Anne Slavotinek

Anne Slavotinek

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Developmental and epileptic encephalopathy in two siblings with a novel, homozygous missense variant in SCN1B.

Am J Med Genet A 2019 Nov 29;179(11):2190-2195. Epub 2019 Aug 29.

Institute for Human Genetics, University of California San Francisco, San Francisco, California.

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http://dx.doi.org/10.1002/ajmg.a.61344DOI Listing
November 2019

Genetics of anophthalmia and microphthalmia. Part 2: Syndromes associated with anophthalmia-microphthalmia.

Authors:
Anne Slavotinek

Hum Genet 2019 Sep 30;138(8-9):831-846. Epub 2018 Oct 30.

Division of Genetics, Department of Pediatrics, University of California, San Francisco Room RH384C, 1550 4th St, San Francisco, CA, 94143-2711, USA.

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http://link.springer.com/10.1007/s00439-018-1949-1
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http://dx.doi.org/10.1007/s00439-018-1949-1DOI Listing
September 2019

TASP1 mutation in a female with craniofacial anomalies, anterior segment dysgenesis, congenital immunodeficiency and macrocytic anemia.

Mol Genet Genomic Med 2019 Sep 27;7(9):e818. Epub 2019 Jul 27.

Division of Plastic and Reconstructive Surgery, Department of Surgery, University of California San Francisco, San Francisco, California.

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http://dx.doi.org/10.1002/mgg3.818DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6732342PMC
September 2019

Perspectives of US private payers on insurance coverage for pediatric and prenatal exome sequencing: Results of a study from the Program in Prenatal and Pediatric Genomic Sequencing (P3EGS).

Genet Med 2019 Sep 10. Epub 2019 Sep 10.

Department of Clinical Pharmacy, Center for Translational and Policy Research on Personalized Medicine (TRANSPERS), UCSF Philip R. Lee Institute for Health Policy, and UCSF Helen Diller Family Comprehensive Cancer Center, University of California-San Francisco, San Francisco, CA, USA.

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http://dx.doi.org/10.1038/s41436-019-0650-7DOI Listing
September 2019

Introducing in AJMG Part A: Genetic Syndromes in Adults.

Am J Med Genet A 2019 Aug 26;179(8):1413-1414. Epub 2019 Mar 26.

Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland.

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http://dx.doi.org/10.1002/ajmg.a.61141DOI Listing
August 2019

Case Report of Floating-Harbor Syndrome With Bilateral Cleft Lip.

Cleft Palate Craniofac J 2019 Jun 27:1055665619858257. Epub 2019 Jun 27.

1 Program in Craniofacial Biology and Division of Craniofacial Anomalies, Department of Orofacial Sciences, University of California, San Francisco, CA, USA.

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http://dx.doi.org/10.1177/1055665619858257DOI Listing
June 2019

Use of PTC124 for nonsense suppression therapy targeting BMP4 nonsense variants in vitro and the bmp4st72 allele in zebrafish.

PLoS One 2019 24;14(4):e0212121. Epub 2019 Apr 24.

Division of Genetics, Department of Pediatrics, University of California San Francisco, San Francisco, CA, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0212121PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6481805PMC
April 2019

Private payer coverage policies for exome sequencing (ES) in pediatric patients: trends over time and analysis of evidence cited.

Genet Med 2019 01 12;21(1):152-160. Epub 2018 Jul 12.

University of California at San Francisco, Department of Clinical Pharmacy; Center for Translational and Policy Research on Personalized Medicine (TRANSPERS); UCSF Philip R. Lee Institute for Health Policy; and UCSF Helen Diller Family Comprehensive Cancer Center, San Francisco, California, USA.

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http://dx.doi.org/10.1038/s41436-018-0043-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6329652PMC
January 2019

Two patients with FOXF1 mutations with alveolar capillary dysplasia with misalignment of pulmonary veins and other malformations: Two different presentations and outcomes.

Am J Med Genet A 2018 12 31;176(12):2877-2881. Epub 2018 Oct 31.

Division of Medical Genetics, Department of Pediatrics, University of California San Francisco, San Francisco, California.

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http://doi.wiley.com/10.1002/ajmg.a.40641
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http://dx.doi.org/10.1002/ajmg.a.40641DOI Listing
December 2018

Early inspirations from times gone by.

Am J Med Genet A 2018 Sep 31;176(9):1797-1798. Epub 2018 Jul 31.

National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland.

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http://doi.wiley.com/10.1002/ajmg.a.40474
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http://dx.doi.org/10.1002/ajmg.a.40474DOI Listing
September 2018

PHENOTYPIC HETEROGENEITY IN A FAMILY WITH X-LINKED FAMILIAL EXUDATIVE VITREORETINOPATHY WITH PREVENTION OF VISUAL LOSS IN AN AFFECTED MALE CHILD WITH LASER TREATMENT IN INFANCY.

Retin Cases Brief Rep 2018 Aug 1. Epub 2018 Aug 1.

Ophthalmology Department, University of California School of Medicine, San Francisco, Koret Vision Research Center, San Francisco, California.

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http://dx.doi.org/10.1097/ICB.0000000000000796DOI Listing
August 2018

Mutation update of transcription factor genes FOXE3, HSF4, MAF, and PITX3 causing cataracts and other developmental ocular defects.

Hum Mutat 2018 04 16;39(4):471-494. Epub 2018 Jan 16.

Department of Biological Sciences, University of Delaware, Newark, Delaware.

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http://dx.doi.org/10.1002/humu.23395DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5839989PMC
April 2018

Inner retinal dystrophy in a patient with biallelic sequence variants in BRAT1.

Ophthalmic Genet 2017 12 2;38(6):559-561. Epub 2017 Mar 2.

a Department of Ophthalmology , University of California , San Francisco, San Francisco , California , USA.

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http://dx.doi.org/10.1080/13816810.2017.1290118DOI Listing
December 2017

HLX is a candidate gene for a pattern of anomalies associated with congenital diaphragmatic hernia, short bowel, and asplenia.

Am J Med Genet A 2017 Nov 12;173(11):3070-3074. Epub 2017 Sep 12.

Molecular Genetics of Development Laboratory, Department of Biological Sciences and BioMed Research Center, Faculty of Sciences, University of Quebec at Montreal, Montreal, Quebec.

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http://dx.doi.org/10.1002/ajmg.a.38354DOI Listing
November 2017

Clinical Report: Warsaw Breakage Syndrome with small radii and fibulae.

Am J Med Genet A 2017 Nov 28;173(11):3075-3081. Epub 2017 Sep 28.

Division of Genetics, Department of Pediatrics, University of California, San Francisco, California.

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http://dx.doi.org/10.1002/ajmg.a.38382DOI Listing
November 2017

Pierpont syndrome associated with the p.Tyr446Cys missense mutation in TBL1XR1.

Eur J Med Genet 2017 Oct 4;60(10):504-508. Epub 2017 Jul 4.

Division of Medical Genetics, Department of Pediatrics, UCSF, San Francisco, CA 94143-2711, USA.

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http://dx.doi.org/10.1016/j.ejmg.2017.07.003DOI Listing
October 2017

Characterization of a variant of gap junction protein α8 identified in a family with hereditary cataract.

PLoS One 2017 21;12(8):e0183438. Epub 2017 Aug 21.

Department of Ophthalmology, University of California, San Francisco School of Medicine, San Francisco, CA, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0183438PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5565107PMC
October 2017

The focal facial dermal dysplasias: phenotypic spectrum and molecular genetic heterogeneity.

J Med Genet 2017 09 29;54(9):585-590. Epub 2017 Jun 29.

Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, USA.

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http://dx.doi.org/10.1136/jmedgenet-2017-104561DOI Listing
September 2017

Clinical report: A patient with a late diagnosis of cerebrotendinous xanthomatosis and a response to treatment.

Am J Med Genet A 2017 Aug 7;173(8):2275-2279. Epub 2017 Jun 7.

Department of Pediatrics,, Division of Genetics, University of California, San Francisco, California.

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http://dx.doi.org/10.1002/ajmg.a.38314DOI Listing
August 2017

Jejunal atresia and unilateral postaxial polydactyly: second report of a rare association.

Clin Dysmorphol 2017 Apr;26(2):132-133

Department of Pediatrics, Division of Genetics, University of California, San Francisco, California, USA.

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http://dx.doi.org/10.1097/MCD.0000000000000167DOI Listing
April 2017

Pregnancy and Birth Outcomes among Women with Idiopathic Thrombocytopenic Purpura.

J Pregnancy 2016 22;2016:8297407. Epub 2016 Mar 22.

Epidemiology, OptumInsight, Waltham, MA 02451, USA; Department of Medicine, Division of Pharmacoeconomics and Pharmacoepidemiology, Brigham & Women's Hospital, Harvard Medical School, Boston, MA 02120, USA.

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http://dx.doi.org/10.1155/2016/8297407DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820621PMC
December 2016

Challenges managing end-stage renal disease and kidney transplantation in a child with MTFMT mutation and moyamoya disease.

Pediatr Transplant 2016 Nov 8;20(7):1000-1003. Epub 2016 Jul 8.

Division of Nephrology, Department of Pediatrics, University of California, San Francisco, San Francisco, CA, USA.

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http://dx.doi.org/10.1111/petr.12758DOI Listing
November 2016

Corneal clouding, cataract, and colobomas with a novel missense mutation in B4GALT7-a review of eye anomalies in the linkeropathy syndromes.

Am J Med Genet A 2016 10 20;170(10):2711-8. Epub 2016 Jun 20.

Division of Genetics, Department of Pediatrics, University of California, San Francisco, California.

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http://dx.doi.org/10.1002/ajmg.a.37809DOI Listing
October 2016

The Family of Crumbs Genes and Human Disease.

Mol Syndromol 2016 Oct 18;7(5):274-281. Epub 2016 Aug 18.

Department of Pediatrics, UCSF School of Medicine, University of California San Francisco, San Francisco, Calif., USA.

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http://dx.doi.org/10.1159/000448109DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5109986PMC
October 2016

An emerging, recognizable facial phenotype in association with mutations in GLI-similar 3 (GLIS3).

Am J Med Genet A 2016 07 5;170(7):1918-23. Epub 2016 May 5.

Sheffield Clinical Genetics Service, Sheffield Children's NHS Foundation Trust, United Kingdom.

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http://dx.doi.org/10.1002/ajmg.a.37680DOI Listing
July 2016

Clinical care models in the era of next-generation sequencing.

Authors:
Anne Slavotinek

Mol Genet Genomic Med 2016 May 12;4(3):239-42. Epub 2016 May 12.

UCSF Benioff Children's Hospital University of California, San Francisco Room 384D, Rock Hall, 1550 4th St San Francisco California 94143-2711.

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http://dx.doi.org/10.1002/mgg3.225DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4867557PMC
May 2016

Pregnancy outcomes following exposure to onabotulinumtoxinA.

Pharmacoepidemiol Drug Saf 2016 Feb 4;25(2):179-87. Epub 2015 Dec 4.

Allergan, Inc., Irvine, CA, USA.

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http://dx.doi.org/10.1002/pds.3920DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5063122PMC
February 2016

Novel KIF7 missense substitutions in two patients presenting with multiple malformations and features of acrocallosal syndrome.

Am J Med Genet A 2015 Nov 14;167A(11):2767-76. Epub 2015 Jul 14.

Division of Genetics, Department of Pediatrics, University of California, San Francisco, California.

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http://dx.doi.org/10.1002/ajmg.a.37249DOI Listing
November 2015

DLX4 is associated with orofacial clefting and abnormal jaw development.

Hum Mol Genet 2015 Aug 7;24(15):4340-52. Epub 2015 May 7.

Department of Pediatrics, University of California, San Francisco, San Francisco, CA 94143, USA, Institute for Human Genetics, University of California, San Francisco, San Francisco, CA, USA,

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http://dx.doi.org/10.1093/hmg/ddv167DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4492397PMC
August 2015

Haploinsufficiency and triploinsensitivity of the same 6p25.1p24.3 region in a family.

BMC Med Genomics 2015 Jul 15;8:38. Epub 2015 Jul 15.

Department of Laboratory Medicine, University of California San Francisco, San Francisco, CA, 94107, USA.

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http://dx.doi.org/10.1186/s12920-015-0113-1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4502905PMC
July 2015

Recognizable syndromes in the newborn period.

Clin Perinatol 2015 Jun 7;42(2):263-80, viii. Epub 2015 Apr 7.

Division of Genetics, Department of Pediatrics, University of California, San Francisco, 1550 4th Street, Room RH384D, San Francisco, CA 94143-2711, USA.

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https://linkinghub.elsevier.com/retrieve/pii/S00955108150002
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http://dx.doi.org/10.1016/j.clp.2015.02.003DOI Listing
June 2015

Expanding the phenotypic spectrum of PORCN variants in two males with syndromic microphthalmia.

Eur J Hum Genet 2015 Apr 16;23(4):551-4. Epub 2014 Jul 16.

Center for Human Genetics, University Hospital Leuven, KU Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1038/ejhg.2014.135DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4666577PMC
April 2015

Novel mutations in PXDN cause microphthalmia and anterior segment dysgenesis.

Eur J Hum Genet 2015 Mar 18;23(3):337-41. Epub 2014 Jun 18.

Department of Pediatrics, Division of Genetics, University of California, San Francisco, CA, USA.

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http://www.nature.com/articles/ejhg2014119
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http://dx.doi.org/10.1038/ejhg.2014.119DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4326713PMC
March 2015

CRB2 mutations produce a phenotype resembling congenital nephrosis, Finnish type, with cerebral ventriculomegaly and raised alpha-fetoprotein.

Am J Hum Genet 2015 Jan 31;96(1):162-9. Epub 2014 Dec 31.

Division of Medical Genetics, Icahn School of Medicine at Mount Sinai & Mount Sinai Medical Center, 1 Gustave Levy Place, New York, NY 10029, USA.

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http://dx.doi.org/10.1016/j.ajhg.2014.11.013DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4289687PMC
January 2015

The FgfrL1 receptor is required for development of slow muscle fibers.

Dev Biol 2014 Oct 27;394(2):228-41. Epub 2014 Aug 27.

Department of Clinical Research, University of Bern, 3010 Bern, Switzerland; Department of Rheumatology, University Hospital, 3010 Bern, Switzerland. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S00121606140040
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http://dx.doi.org/10.1016/j.ydbio.2014.08.016DOI Listing
October 2014

The genetics of common disorders - congenital diaphragmatic hernia.

Eur J Med Genet 2014 Aug 2;57(8):418-23. Epub 2014 May 2.

Department of Pediatrics, Division of Genetics, University of California, MSC 2711, Rock Hall Room RH384D, 1550 4th St, San Francisco, CA 94143-2711, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ejmg.2014.04.012DOI Listing
August 2014

Nine patients with Xp22.31 microduplication, cognitive deficits, seizures, and talipes anomalies.

Am J Med Genet A 2014 Aug 6;164A(8):2097-103. Epub 2014 May 6.

Division of Medical Genetics, Department of Pediatrics, Stanford University School of Medicine, Stanford, California.

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http://dx.doi.org/10.1002/ajmg.a.36598DOI Listing
August 2014

Advanced bone age in a girl with Wiedemann-Steiner syndrome and an exonic deletion in KMT2A (MLL).

Am J Med Genet A 2014 Aug 12;164A(8):2079-83. Epub 2014 May 12.

Division of Genetics, Department of Pediatrics, University of California San Francisco, San Francisco, California.

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http://doi.wiley.com/10.1002/ajmg.a.36590
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http://dx.doi.org/10.1002/ajmg.a.36590DOI Listing
August 2014

De novo ANKRD11 and KDM1A gene mutations in a male with features of KBG syndrome and Kabuki syndrome.

Am J Med Genet A 2014 Jul 16;164A(7):1744-9. Epub 2014 May 16.

Department of Pediatrics and Institute for Human Genetics, University of California, San Francisco, San Francisco, California.

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http://dx.doi.org/10.1002/ajmg.a.36450DOI Listing
July 2014

Clinical report: Two patients with atelosteogenesis type I caused by missense mutations affecting the same FLNB residue.

Am J Med Genet A 2013 Mar 11;161A(3):619-25. Epub 2013 Feb 11.

Division of Genetics, Department of Pediatrics, University of California, San Francisco, California 94143-0748, USA.

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http://dx.doi.org/10.1002/ajmg.a.35792DOI Listing
March 2013

2p16.3 microdeletion with partial deletion of the neurexin-1 gene in a female with developmental delays, short stature, and a congenital diaphragmatic hernia.

Clin Dysmorphol 2013 Jan;22(1):22-4

Department of Pediatrics, Division of Genetics, University of California, San Francisco, CA 94143-0748, USA.

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http://dx.doi.org/10.1097/MCD.0b013e32835b8df2DOI Listing
January 2013

Intraparenchymal hemorrhage in a neonate with cleidocranial dysostosis.

Pediatr Neurol 2012 Dec;47(6):455-7

Department of Neurology, University of California at San Francisco, San Francisco, California, USA.

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http://dx.doi.org/10.1016/j.pediatrneurol.2012.08.009DOI Listing
December 2012

Congenital high airway obstruction sequence (CHAOS): a new case and a review of phenotypic features.

Am J Med Genet A 2012 Dec 19;158A(12):3126-36. Epub 2012 Nov 19.

Division of Medical Genetics, Department of Pediatrics, University of California, San Francisco, California 94143-0748, USA.

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http://doi.wiley.com/10.1002/ajmg.a.35643
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http://dx.doi.org/10.1002/ajmg.a.35643DOI Listing
December 2012

Special Section. Syndrome-specific growth charts.

Am J Med Genet A 2012 Nov 4;158A(11):2645-6. Epub 2012 Oct 4.

Department of Medical Genetics and Pediatrics, University of British Columbia and BC Children's Hospital Vancouver, British Columbia, Canada.

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http://doi.wiley.com/10.1002/ajmg.a.35704
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http://dx.doi.org/10.1002/ajmg.a.35704DOI Listing
November 2012

A much needed new journal in the field of Pediatric Genetics.

J Pediatr Genet 2012 Mar;1(1):1-2

Department of Pediatrics, Division of Genetics, University of California, San Francisco, CA, USA.

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http://dx.doi.org/10.3233/PGE-2012-001DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5020911PMC
March 2012

Eye development genes and known syndromes.

Mol Genet Metab 2011 Dec 29;104(4):448-56. Epub 2011 Sep 29.

Department of Pediatrics, Division of Genetics, University of California, San Francisco, San Francisco, CA 94143-0748, USA.

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https://linkinghub.elsevier.com/retrieve/pii/S10967192110034
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http://dx.doi.org/10.1016/j.ymgme.2011.09.029DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3224152PMC
December 2011

Targeted 'next-generation' sequencing in anophthalmia and microphthalmia patients confirms SOX2, OTX2 and FOXE3 mutations.

BMC Med Genet 2011 Dec 28;12:172. Epub 2011 Dec 28.

Department of Pediatrics, Division of Genetics, University of California, San Francisco, 533 Parnassus St, Room U585P, San Francisco, CA 94143-0748 USA.

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http://dx.doi.org/10.1186/1471-2350-12-172DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3262754PMC
December 2011

Congenital diaphragmatic hernia in Smith-Magenis syndrome: a possible locus at chromosome 17p11.2.

Am J Med Genet A 2011 Nov 30;155A(11):2816-20. Epub 2011 Sep 30.

Department of Pediatrics, Division of Genetics, University of California, San Francisco, San Francisco, California 94143-0748, USA.

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http://dx.doi.org/10.1002/ajmg.a.34247DOI Listing
November 2011

A de novo deletion of CALN1 in a male with a bilateral diaphragmatic defect does not definitely cause this malformation.

Am J Med Genet A 2011 May 7;155A(5):1196-201. Epub 2011 Apr 7.

Division of Genetics, Department of Pediatrics, University of California, San Francisco, 94143-0748, USA.

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http://dx.doi.org/10.1002/ajmg.a.34002DOI Listing
May 2011

Clinical utility gene card for: Bardet-Biedl syndrome.

Eur J Hum Genet 2011 Mar 8;19(3). Epub 2010 Dec 8.

Division of Genetics, Department of Pediatrics, University of California, San Francisco, San Francisco, CA 94143, USA.

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http://dx.doi.org/10.1038/ejhg.2010.199DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3061994PMC
March 2011

Expanded spectrum of oculo-auriculo-vertebral spectrum with imperforate anus in a male patient who is negative for SALL1 mutations.

Clin Dysmorphol 2011 Jan;20(1):11-4

Department of Pediatrics, Division of Clinical Genetics, University of California, San Francisco, California 94143-0748, USA.

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http://dx.doi.org/10.1097/mcd.0b013e32833f138cDOI Listing
January 2011

Clinical report of microphthalmia and optic nerve coloboma associated with a de novo microdeletion of chromosome 16p11.2.

Am J Med Genet A 2010 Dec;152A(12):3120-3

Division of Genetics, Department of Pediatrics, Albert Einstein Medical Center, Philadelphia, Pennsylvania 19141, USA.

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http://dx.doi.org/10.1002/ajmg.a.33492DOI Listing
December 2010

A novel EFNB1 mutation (c.712delG) in a family with craniofrontonasal syndrome and diaphragmatic hernia.

Am J Med Genet A 2010 Oct;152A(10):2574-7

Department of Pediatrics, University of California, San Francisco, California 94143-0706, USA.

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http://dx.doi.org/10.1002/ajmg.a.33596DOI Listing
October 2010

Saethre-Chotzen syndrome: a case report.

Cleft Palate Craniofac J 2010 May;47(3):318-21

Division of Pediatric Dentistry, Department of Orofacial Sciences, School of Dentistry, University of California at San Francisco, San Francisco, California, USA.

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http://dx.doi.org/10.1597/07-202.1DOI Listing
May 2010

Hypodontia in Beare-Stevenson syndrome: an example of dental anomalies in FGFR-related craniosynostosis syndromes.

Cleft Palate Craniofac J 2010 May;47(3):253-8

UCSF School of Dentistry, San Francisco, California, USA.

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http://journals.sagepub.com/doi/10.1597/08-282.1
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http://dx.doi.org/10.1597/08-282.1DOI Listing
May 2010

Novel FGFR2 deletion in a patient with Beare-Stevenson-like syndrome.

Am J Med Genet A 2009 Aug;149A(8):1814-7

Department of Pediatrics, University of California, San Francisco, 94143-0748, USA.

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http://dx.doi.org/10.1002/ajmg.a.32947DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2785435PMC
August 2009

Congenital diaphragmatic hernia and microtia in a newborn with mycophenolate mofetil (MMF) exposure: phenocopy for Fryns syndrome or broad spectrum of teratogenic effects?

Am J Med Genet A 2009 Jun;149A(6):1237-40

Department of Pediatrics, Seattle Children's Hospital, University of Washington, Seattle, Washington 98105, USA.

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http://dx.doi.org/10.1002/ajmg.a.32684DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2692642PMC
June 2009