Karen W Gripp

Karen W Gripp

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Karen W Gripp

Publications by authors named "Karen W Gripp"

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Costello syndrome: Clinical phenotype, genotype, and management guidelines.

Am J Med Genet A 2019 Sep 20;179(9):1725-1744. Epub 2019 Jun 20.

Division of Genomic Medicine, Department of Pediatrics, University of California Davis, Sacramento, California.

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http://dx.doi.org/10.1002/ajmg.a.61270DOI Listing
September 2019

PEDIA: prioritization of exome data by image analysis.

Genet Med 2019 Jun 5. Epub 2019 Jun 5.

Institute of Genomic Statistics and Bioinformatics, University of Bonn, Bonn, Germany.

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http://dx.doi.org/10.1038/s41436-019-0566-2DOI Listing
June 2019

Identifying facial phenotypes of genetic disorders using deep learning.

Nat Med 2019 01 7;25(1):60-64. Epub 2019 Jan 7.

Division of Medical Genetics, A. I. du Pont Hospital for Children/Nemours, Wilmington, DE, USA.

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http://dx.doi.org/10.1038/s41591-018-0279-0DOI Listing
January 2019

Imaging phenotype of multiple mitochondrial dysfunction syndrome 2, a rare BOLA3-associated leukodystrophy.

Am J Med Genet A 2018 12 10;176(12):2787-2790. Epub 2018 Oct 10.

Department of Medical Imaging, Nemours A I duPont Hospital for Children, Wilmington, Delaware.

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http://dx.doi.org/10.1002/ajmg.a.40490DOI Listing
December 2018

Urine cell-free DNA is a biomarker for nephroblastomatosis or Wilms tumor in PIK3CA-related overgrowth spectrum (PROS).

Genet Med 2018 09 4;20(9):1077-1081. Epub 2018 Jan 4.

Medical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.

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http://dx.doi.org/10.1038/gim.2017.228DOI Listing
September 2018

Further delineation of Aymé-Gripp syndrome and use of automated facial analysis tool.

Am J Med Genet A 2018 07;176(7):1648-1656

A. I. du Pont Hospital for Children/Nemours, Wilmington, Delaware.

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http://doi.wiley.com/10.1002/ajmg.a.38832
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http://dx.doi.org/10.1002/ajmg.a.38832DOI Listing
July 2018

Ribosome Levels Selectively Regulate Translation and Lineage Commitment in Human Hematopoiesis.

Cell 2018 03 15;173(1):90-103.e19. Epub 2018 Mar 15.

Division of Hematology/Oncology, Boston Children's Hospital and Department of Pediatric Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02115, USA; Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA. Electronic address:

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http://dx.doi.org/10.1016/j.cell.2018.02.036DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5866246PMC
March 2018

Genotype-Phenotype Correlation in NF1: Evidence for a More Severe Phenotype Associated with Missense Mutations Affecting NF1 Codons 844-848.

Am J Hum Genet 2018 01 28;102(1):69-87. Epub 2017 Dec 28.

Department of Genetics, University of Alabama at Birmingham, Birmingham, AL 35294, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2017.12.001DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5777934PMC
January 2018

Computational Prediction of Position Effects of Apparently Balanced Human Chromosomal Rearrangements.

Am J Hum Genet 2017 Aug 20;101(2):206-217. Epub 2017 Jul 20.

Department of Obstetrics, Gynecology, and Reproductive Biology, Brigham and Women's Hospital, Boston, MA 02115, USA; Johannes Gutenberg University, Mainz 55122, Germany; Program in Medical and Population Genetics, Broad Institute of Harvard and MIT, Cambridge, MA 02142, USA; Department of Pathology, Brigham and Women's Hospital, Boston, MA 02115, USA; Division of Evolution and Genomic Science, School of Biological Sciences, Manchester Academic Health Science Centre, Manchester M13 9NT, UK. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S00029297173024
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http://dx.doi.org/10.1016/j.ajhg.2017.06.011DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5544382PMC
August 2017

Phenotypic spectrum of Costello syndrome individuals harboring the rare HRAS mutation p.Gly13Asp.

Am J Med Genet A 2017 May 3;173(5):1309-1318. Epub 2017 Apr 3.

Center for Applied Clinical Genomics, A. I. duPont Hospital for Children/Nemours, Wilmington, Delaware.

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http://dx.doi.org/10.1002/ajmg.a.38178DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5397353PMC
May 2017

Age-related differences in prevalence of autism spectrum disorder symptoms in children and adolescents with Costello syndrome.

Am J Med Genet A 2017 May 4;173(5):1294-1300. Epub 2017 Apr 4.

Section of Psychology, Department of Pediatrics, Baylor College of Medicine, Texas Children's Hospital, Houston, Texas.

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http://dx.doi.org/10.1002/ajmg.a.38174DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5397350PMC
May 2017

A novel patient with an attenuated Costello syndrome phenotype due to an HRAS mutation affecting codon 146-Literature review and update.

Am J Med Genet A 2017 Apr;173(4):1109-1114

Department of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong, China.

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http://dx.doi.org/10.1002/ajmg.a.38118DOI Listing
April 2017

Cytotoxicity of Zardaverine in Embryonal Rhabdomyosarcoma from a Costello Syndrome Patient.

Front Oncol 2017 3;7:42. Epub 2017 Apr 3.

High-Throughput Screening and Drug Discovery Laboratory, Nemours Center for Childhood Cancer Research, Nemours Biomedical Research, Nemours/A.I. duPont Hospital for Children, Wilmington, DE, USA.

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http://dx.doi.org/10.3389/fonc.2017.00042DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5376947PMC
April 2017

Elucidation of -mediated Noonan syndrome with cardiac hypertrophy.

JCI Insight 2017 03 9;2(5):e91225. Epub 2017 Mar 9.

Department of Molecular Pharmacology and Experimental Therapeutics and Windland Smith Rice Sudden Death Genomics Laboratory.

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http://dx.doi.org/10.1172/jci.insight.91225DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5333962PMC
March 2017

The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies.

Authors:
Claire Redin Harrison Brand Ryan L Collins Tammy Kammin Elyse Mitchell Jennelle C Hodge Carrie Hanscom Vamsee Pillalamarri Catarina M Seabra Mary-Alice Abbott Omar A Abdul-Rahman Erika Aberg Rhett Adley Sofia L Alcaraz-Estrada Fowzan S Alkuraya Yu An Mary-Anne Anderson Caroline Antolik Kwame Anyane-Yeboa Joan F Atkin Tina Bartell Jonathan A Bernstein Elizabeth Beyer Ian Blumenthal Ernie M H F Bongers Eva H Brilstra Chester W Brown Hennie T Brüggenwirth Bert Callewaert Colby Chiang Ken Corning Helen Cox Edwin Cuppen Benjamin B Currall Tom Cushing Dezso David Matthew A Deardorff Annelies Dheedene Marc D'Hooghe Bert B A de Vries Dawn L Earl Heather L Ferguson Heather Fisher David R FitzPatrick Pamela Gerrol Daniela Giachino Joseph T Glessner Troy Gliem Margo Grady Brett H Graham Cristin Griffis Karen W Gripp Andrea L Gropman Andrea Hanson-Kahn David J Harris Mark A Hayden Rosamund Hill Ron Hochstenbach Jodi D Hoffman Robert J Hopkin Monika W Hubshman A Micheil Innes Mira Irons Melita Irving Jessie C Jacobsen Sandra Janssens Tamison Jewett John P Johnson Marjolijn C Jongmans Stephen G Kahler David A Koolen Jerome Korzelius Peter M Kroisel Yves Lacassie William Lawless Emmanuelle Lemyre Kathleen Leppig Alex V Levin Haibo Li Hong Li Eric C Liao Cynthia Lim Edward J Lose Diane Lucente Michael J Macera Poornima Manavalan Giorgia Mandrile Carlo L Marcelis Lauren Margolin Tamara Mason Diane Masser-Frye Michael W McClellan Cinthya J Zepeda Mendoza Björn Menten Sjors Middelkamp Liya R Mikami Emily Moe Shehla Mohammed Tarja Mononen Megan E Mortenson Graciela Moya Aggie W Nieuwint Zehra Ordulu Sandhya Parkash Susan P Pauker Shahrin Pereira Danielle Perrin Katy Phelan Raul E Piña Aguilar Pino J Poddighe Giulia Pregno Salmo Raskin Linda Reis William Rhead Debra Rita Ivo Renkens Filip Roelens Jayla Ruliera Patrick Rump Samantha L P Schilit Ranad Shaheen Rebecca Sparkes Erica Spiegel Blair Stevens Matthew R Stone Julia Tagoe Joseph V Thakuria Bregje W van Bon Jiddeke van de Kamp Ineke van Der Burgt Ton van Essen Conny M van Ravenswaaij-Arts Markus J van Roosmalen Sarah Vergult Catharina M L Volker-Touw Dorothy P Warburton Matthew J Waterman Susan Wiley Anna Wilson Maria de la Concepcion A Yerena-de Vega Roberto T Zori Brynn Levy Han G Brunner Nicole de Leeuw Wigard P Kloosterman Erik C Thorland Cynthia C Morton James F Gusella Michael E Talkowski

Nat Genet 2017 01 14;49(1):36-45. Epub 2016 Nov 14.

Molecular Neurogenetics Unit, Center for Human Genetic Research, Department of Neurology, Massachusetts General Hospital, Boston, Massachusetts, USA.

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http://dx.doi.org/10.1038/ng.3720DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5307971PMC
January 2017

36th Annual David W. Smith Workshop on Malformations and Morphogenesis: Abstracts of the 2015 annual meeting.

Am J Med Genet A 2016 Jul 27;170(7):1665-726. Epub 2016 Apr 27.

Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah.

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http://dx.doi.org/10.1002/ajmg.a.37600DOI Listing
July 2016

Differentiating between copy-number-variation and gain-of-function mutation.

Authors:
Karen W Gripp

Am J Med Genet A 2015 Nov 2;167A(11):2684. Epub 2015 Jul 2.

Division of Medical Genetics, AI duPont Hospital for Children/Nemours, Wilmington, Delaware.

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http://dx.doi.org/10.1002/ajmg.a.37220DOI Listing
November 2015

High Incidence of Noonan Syndrome Features Including Short Stature and Pulmonic Stenosis in Patients carrying NF1 Missense Mutations Affecting p.Arg1809: Genotype-Phenotype Correlation.

Hum Mutat 2015 Nov 21;36(11):1052-63. Epub 2015 Aug 21.

Department of Genetics, Medical Genomics Laboratory, University of Alabama at Birmingham, Birmingham, Alabama.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5049609PMC
http://dx.doi.org/10.1002/humu.22832DOI Listing
November 2015

Truncating mutations in the last exon of NOTCH3 cause lateral meningocele syndrome.

Am J Med Genet A 2015 Feb 13;167A(2):271-81. Epub 2014 Nov 13.

Division of Medical Genetics, A.I. duPont Hospital for Children, Wilmington, Delaware, and Sidney Kimmel Medical School at T. Jefferson University, Philadelphia, Pennsylvania.

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http://dx.doi.org/10.1002/ajmg.a.36863DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5589071PMC
February 2015

Neuromotor synapses in Escobar syndrome.

Am J Med Genet A 2013 Dec 16;161A(12):3042-8. Epub 2013 Aug 16.

Nemours Biomedical Research, Alfred I. duPont Hospital for Children, Wilmington, Delaware.

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http://dx.doi.org/10.1002/ajmg.a.36154DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5600816PMC
December 2013

Constitutional mismatch repair deficiency presenting in childhood as three simultaneous malignancies.

Pediatr Blood Cancer 2013 Nov 1;60(11):E135-6. Epub 2013 Jun 1.

Department of Pediatrics, Jefferson Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania; Department of Pediatrics, A. I. duPont Hospital for Children, Wilmington, Delaware.

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http://dx.doi.org/10.1002/pbc.24613DOI Listing
November 2013

Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autism.

Nat Genet 2013 Nov 29;45(11):1405-8. Epub 2013 Sep 29.

1] Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA. [2] Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, Texas, USA. [3].

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http://www.nature.com/articles/ng.2776
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http://dx.doi.org/10.1038/ng.2776DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3819162PMC
November 2013

Verbal memory functioning in adolescents and young adults with Costello syndrome: evidence for relative preservation in recognition memory.

Am J Med Genet A 2013 Sep 5;161A(9):2258-65. Epub 2013 Aug 5.

Section of Psychology, Department of Pediatrics, Baylor College of Medicine/Texas Children's Hospital, Houston, Texas 77030, USA.

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http://dx.doi.org/10.1002/ajmg.a.36078DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3745536PMC
September 2013

Orthopedic manifestations and implications for individuals with Costello syndrome.

Am J Med Genet A 2013 Aug 27;161A(8):1940-9. Epub 2013 Jun 27.

Genetic Counseling Program, Arcadia University, Glenside, PA, USA.

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http://dx.doi.org/10.1002/ajmg.a.36047DOI Listing
August 2013

Assessing genotype-phenotype correlation in Costello syndrome using a severity score.

Genet Med 2013 Jul 21;15(7):554-7. Epub 2013 Feb 21.

Division of Medical Genetics, Alfred I. duPont Hospital for Children, Wilmington, Delaware, USA.

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http://dx.doi.org/10.1038/gim.2013.6DOI Listing
July 2013

Keratoconus in Costello syndrome.

Am J Med Genet A 2013 May 13;161A(5):1132-6. Epub 2013 Mar 13.

Division of Medical Genetics, A. I. duPont Hospital for Children, Wilmington, DE, USA.

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http://dx.doi.org/10.1002/ajmg.a.35816DOI Listing
May 2013

Exome analysis in clinical practice: expanding the phenotype of Bartsocas-Papas syndrome.

Am J Med Genet A 2013 May;161A(5):1058-63

Division of Medical Genetics, A. I. duPont Hospital for Children, Wilmington, DE 19803, USA.

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http://dx.doi.org/10.1002/ajmg.a.35913DOI Listing
May 2013

Cardiac anomalies in Axenfeld-Rieger syndrome due to a novel FOXC1 mutation.

Am J Med Genet A 2013 Jan 14;161A(1):114-9. Epub 2012 Dec 14.

Division of Medical Genetics, A. I. DuPont Hospital for Children, Wilmington, Delaware.

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http://dx.doi.org/10.1002/ajmg.a.35697DOI Listing
January 2013

Normative growth charts for individuals with Costello syndrome.

Am J Med Genet A 2012 Nov 7;158A(11):2692-9. Epub 2012 Aug 7.

Division of General Pediatrics, A. I. duPont Hospital for Children, Wilmington, Delaware 19803, USA.

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http://doi.wiley.com/10.1002/ajmg.a.35534
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http://dx.doi.org/10.1002/ajmg.a.35534DOI Listing
November 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

Transmission of the rare HRAS mutation (c. 173C > T; p.T58I) further illustrates its attenuated phenotype.

Am J Med Genet A 2012 May 9;158A(5):1095-101. Epub 2012 Apr 9.

Division of Medical Genetics, A I duPont Hospital for Children, Wilmington, Delaware 19803, USA.

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http://dx.doi.org/10.1002/ajmg.a.35294DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4164267PMC
May 2012

Costello syndrome: a Ras/mitogen activated protein kinase pathway syndrome (rasopathy) resulting from HRAS germline mutations.

Genet Med 2012 Mar;14(3):285-92

Division of Medical Genetics, Alfred I. duPont Hospital for Children, Wilmington, Delaware, USA.

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http://www.nature.com/articles/gim0b013e31822dd91f
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http://dx.doi.org/10.1038/gim.0b013e31822dd91fDOI Listing
March 2012

Long-term survival in TARP syndrome and confirmation of RBM10 as the disease-causing gene.

Am J Med Genet A 2011 Oct 9;155A(10):2516-20. Epub 2011 Sep 9.

Division of Medical Genetics, A. I. duPont Hospital for Children, Wilmington, Delaware.

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http://dx.doi.org/10.1002/ajmg.a.34190DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3183328PMC
October 2011

Molecular confirmation of HRAS p.G12S in siblings with Costello syndrome.

Am J Med Genet A 2011 Sep 10;155A(9):2263-8. Epub 2011 Aug 10.

Division of Medical Genetics, A I duPont Hospital for Children, Wilmington, Delaware 19803, USA.

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http://dx.doi.org/10.1002/ajmg.a.34150DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3158836PMC
September 2011

Lateral meningocele syndrome and Hajdu-Cheney syndrome: different disorders with overlapping phenotypes.

Authors:
Karen W Gripp

Am J Med Genet A 2011 Jul 10;155A(7):1773-4; author reply 1775. Epub 2011 Jun 10.

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http://dx.doi.org/10.1002/ajmg.a.34075DOI Listing
July 2011

Neurocognitive, adaptive, and behavioral functioning of individuals with Costello syndrome: a review.

Am J Med Genet C Semin Med Genet 2011 May 14;157C(2):115-22. Epub 2011 Apr 14.

Section of Psychology, at Baylor College of Medicine and Clinical Psychologist in the Psychology Service at Texas Children’s Hospital in Houston, Texas, USA.

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http://dx.doi.org/10.1002/ajmg.c.30299DOI Listing
May 2011

CNS imaging is a key diagnostic tool in the evaluation of patients with CFC syndrome: two cases and literature review.

Am J Med Genet A 2011 Mar 18;155A(3):605-11. Epub 2011 Feb 18.

Department of Pediatrics, University Hospital of Heraklion, Crete, Greece.

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http://dx.doi.org/10.1002/ajmg.a.33787DOI Listing
March 2011

Grade 1 microtia, wide anterior fontanel and novel type tracheo-esophageal fistula in methimazole embryopathy.

Am J Med Genet A 2011 Mar 22;155A(3):526-33. Epub 2011 Feb 22.

Division of Medical Genetics, A. I. duPont Hospital for Children, Wilmington, Delaware, USA.

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http://doi.wiley.com/10.1002/ajmg.a.33705
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http://dx.doi.org/10.1002/ajmg.a.33705DOI Listing
March 2011

X-linked hereditary hemihypotrophy hemiparesis hemiathetosis.

Am J Med Genet A 2010 Nov;152A(11):2727-30

Department of Neurology, LSU Health Sciences Center, New Orleans, Louisiana, USA.

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http://dx.doi.org/10.1002/ajmg.a.33545DOI Listing
November 2010

Agenesis of the corpus callosum and congenital lymphedema: A novel recognizable syndrome?

Am J Med Genet A 2010 Jul;152A(7):1621-6

Medical Genetics Research Group and Regional Genetics Service, St Mary's Hospital, Manchester, UK.

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http://dx.doi.org/10.1002/ajmg.a.33200DOI Listing
July 2010

Living with Costello syndrome: quality of life issues in older individuals.

Am J Med Genet A 2010 Jan;152A(1):84-90

Division of Medical Genetics, Alfred I. duPont Hospital for Children, Nemours' Children's Clinic, 1600 Rockland Rd., Wilmington, DE 19803, USA.

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http://dx.doi.org/10.1002/ajmg.a.33147DOI Listing
January 2010

Longitudinal course of cognitive, adaptive, and behavioral characteristics in Costello syndrome.

Am J Med Genet A 2009 Dec;149A(12):2666-72

Psychology Service, Department of Pediatrics, Texas Children's Hospital, Psychology Section, Pediatrics, Baylor College of Medicine, Houston, Texas, USA.

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http://dx.doi.org/10.1002/ajmg.a.33126DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2787985PMC
December 2009

Significant overlap and possible identity of macrocephaly capillary malformation and megalencephaly polymicrogyria-polydactyly hydrocephalus syndromes.

Am J Med Genet A 2009 May;149A(5):868-76

Division of Medical Genetics, Alfred I duPont Hospital for Children, Wilmington, Delaware 19803, USA.

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http://dx.doi.org/10.1002/ajmg.a.32732DOI Listing
May 2009

Preaxial hallucal polydactyly as a marker for diabetic embryopathy.

Birth Defects Res A Clin Mol Teratol 2009 Jan;85(1):13-9

Emory University School of Medicine, Atlanta, Georgia 30033, USA.

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http://dx.doi.org/10.1002/bdra.20503DOI Listing
January 2009

The diagnosis of Costello syndrome: nomenclature in Ras/MAPK pathway disorders.

Am J Med Genet A 2008 May;146A(9):1218-20

Regional Genetic Service and Medical Genetics Research Group, Central Manchester and Manchester Children's Hospitals University NHS Trust, Manchester, UK.

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http://dx.doi.org/10.1002/ajmg.a.32273DOI Listing
May 2008

Expanding the phenotype of SPONASTRIME dysplasia to include short dental roots, hypogammaglobulinemia, and cataracts.

Am J Med Genet A 2008 Feb;146A(4):468-73

Division of Medical Genetics, A. I. duPont Hospital for Children, Wilmington, Delaware 19803, USA.

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http://dx.doi.org/10.1002/ajmg.a.32155DOI Listing
February 2008

Longitudinal assessment of cognitive characteristics in Costello syndrome.

Am J Med Genet A 2007 Dec;143A(24):3185-93

Learning Support Center for Child Psychology, Department of Pediatrics, Texas Children's Hospital, Child Psychology, Allied Health Sciences, Baylor College of Medicine, Houston, Texas, USA.

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http://dx.doi.org/10.1002/ajmg.a.31968DOI Listing
December 2007

Costello syndrome and related disorders.

Curr Opin Pediatr 2007 Dec;19(6):636-44

Division of Medical Genetics, A.I. duPont Hospital for Children, Wilmington, Delaware 19803, USA.

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http://pdfs.journals.lww.com/co-pediatrics/2007/12000/Costel
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http://content.wkhealth.com/linkback/openurl?sid=WKPTLP:land
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http://dx.doi.org/10.1097/MOP.0b013e3282f161dcDOI Listing
December 2007

Hepatoblastoma and heart transplantation in a patient with cardio-facio-cutaneous syndrome.

Am J Med Genet A 2007 Jul;143A(13):1481-8

Department of Pediatrics,University of Virginia Health System, Charlottesville, Virginia.

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http://dx.doi.org/10.1002/ajmg.a.31819DOI Listing
July 2007

Selective IgM deficiency and 22q11.2 deletion syndrome.

Ann Allergy Asthma Immunol 2007 Jul;99(1):87-92

Division of Allergy and Clinical Immunology, Alfred I. DuPont Hospital for Children, Wilmington, Delaware 19899, USA.

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http://dx.doi.org/10.1016/S1081-1206(10)60627-8DOI Listing
July 2007