Virginia P Sybert

Virginia P Sybert

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Virginia P Sybert

Virginia P Sybert

Publications by authors named "Virginia P Sybert"

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Postnatal outcomes of prenatally diagnosed 45,X/46,XX.

Am J Med Genet A 2016 May 20;170A(5):1196-201. Epub 2016 Jan 20.

Division of Medical Genetics, University of Washington, Seattle, Washington.

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http://dx.doi.org/10.1002/ajmg.a.37551DOI Listing
May 2016

So You Want to Be in Journals, or What Happens When You Press "Send".

Pediatr Dermatol 2015 Jul-Aug;32(4):558-61. Epub 2015 Apr 6.

Pediatric Dermatology, Group Health Cooperative, Seattle, Washington.

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http://dx.doi.org/10.1111/pde.12573DOI Listing
April 2016

Ventral midline blanching in the setting of segmental infantile hemangiomas: clinical observations and pathogenetic implications.

Pediatr Dermatol 2015 Mar-Apr;32(2):180-7. Epub 2014 Dec 22.

School of Medicine, University of California, San Diego, San Diego, California.

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http://dx.doi.org/10.1111/pde.12462DOI Listing
December 2015

Actionable exomic incidental findings in 6503 participants: challenges of variant classification.

Genome Res 2015 Mar 30;25(3):305-15. Epub 2015 Jan 30.

Department of Medicine, Division of Medical Genetics, University of Washington, Seattle, Washington 98195, USA; Department of Genome Sciences, University of Washington, Seattle, Washington 98195, USA;

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http://dx.doi.org/10.1101/gr.183483.114DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4352885PMC
March 2015

Genetic counseling in epidermolysis bullosa.

Dermatol Clin 2010 Apr;28(2):239-43, viii

Division of Medical Genetics, University of Washington School of Medicine, Seattle, WA 98195, USA.

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http://dx.doi.org/10.1016/j.det.2009.12.004DOI Listing
April 2010

Dermatologic findings of ankyloblepharon-ectodermal defects-cleft lip/palate (AEC) syndrome.

Am J Med Genet A 2009 Sep;149A(9):1900-6

Texas Children's Hospital, Department of Pediatric Dermatology, Baylor College of Medicine, 6621 Fannin Street, Houston, TX 77030, USA.

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http://doi.wiley.com/10.1002/ajmg.a.32797
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http://dx.doi.org/10.1002/ajmg.a.32797DOI Listing
September 2009

Mosaicism in genetic skin disorders.

Pediatr Dermatol 2006 Jan-Feb;23(1):87-92

Department of Dermatology, University of California San Francisco, San Francisco, California, USA.

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http://dx.doi.org/10.1111/j.1525-1470.2006.00180.xDOI Listing
July 2006

Hereditary woolly hair and keratosis pilaris.

J Am Acad Dermatol 2006 Feb;54(2 Suppl):S35-9

Division of Dermatology, University of Washington, Seattle, Washington, USA.

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https://linkinghub.elsevier.com/retrieve/pii/S01909622050042
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http://dx.doi.org/10.1016/j.jaad.2005.01.092DOI Listing
February 2006

Skin erosions and wound healing in ankyloblepharon-ectodermal defect-cleft lip and/or palate.

Arch Dermatol 2005 Dec;141(12):1591-4

Kids Dermatology, 621 S. New Ballas Road, St. Louis, MO 63141, USA.

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http://dx.doi.org/10.1001/archderm.141.12.1591DOI Listing
December 2005

Understanding aneuploidy.

Pediatr Dermatol 2005 May-Jun;22(3):270-5

Department of Dermatology and Pediatrics, University of California San Francisco, San Francisco, California, USA.

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http://dx.doi.org/10.1111/j.1525-1470.2005.22323.xDOI Listing
August 2005

Mosaicism in cutaneous pigmentation.

Curr Opin Pediatr 2005 Aug;17(4):494-500

Division of Dermatology, Department of Medicine, University of Washington, Department of Dermatology, Group Health Permanente, Seattle, Washington 98195-6524, USA.

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http://dx.doi.org/10.1097/01.mop.0000171319.84053.45DOI Listing
August 2005

Growth characteristics of children with ectodermal dysplasia syndromes.

Pediatrics 2005 Aug;116(2):e229-34

Children's Nutrition Research Center, Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.

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http://dx.doi.org/10.1542/peds.2004-2830DOI Listing
August 2005

Turner's syndrome.

N Engl J Med 2004 Sep;351(12):1227-38

Division of Medical Genetics, Department of Medicine, University of Washington School of Medicine, Seattle, USA.

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http://dx.doi.org/10.1056/NEJMra030360DOI Listing
September 2004

Phenotype and X inactivation in 45,X/46,X,r(X) cases.

Am J Med Genet A 2004 Jul;128A(3):276-84

Genetic Services, Group Health Permanente, Seattle, Washington 98112, USA.

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http://dx.doi.org/10.1002/ajmg.a.30002DOI Listing
July 2004

Genetic heterogeneity of KID syndrome: identification of a Cx30 gene (GJB6) mutation in a patient with KID syndrome and congenital atrichia.

J Invest Dermatol 2004 May;122(5):1108-13

Division of Dermatology, Department of Medicine, University of Washington, Seattle, WA, USA.

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http://dx.doi.org/10.1111/j.0022-202X.2004.22518.xDOI Listing
May 2004

Effects of pregnancy on the renal and pulmonary manifestations in women with tuberous sclerosis complex.

Genet Med 2003 May-Jun;5(3):154-60

Department of Internal Medicine, University of Washington, Seattle, Washington 98105, USA.

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http://dx.doi.org/10.1097/01.GIM.0000066795.92152.67DOI Listing
August 2003

Genetic heterogeneity in erythrokeratodermia variabilis: novel mutations in the connexin gene GJB4 (Cx30.3) and genotype-phenotype correlations.

J Invest Dermatol 2003 Apr;120(4):601-9

Department of Dermatology and Cutaneous Biology, Jefferson Medical College, and Jefferson Institute of Molecular Medicine, Thomas Jefferson University, Philadelphia, Pennsylvania 19107, USA.

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http://dx.doi.org/10.1046/j.1523-1747.2003.12080.xDOI Listing
April 2003

Growth failure in early life: an important manifestation of Turner syndrome.

Horm Res 2002 ;57(5-6):157-64

Department of Pediatrics, Division of Pediatric Endocrinology, School of Public Health, The University of North Carolina at Chapel Hill, NC 27599, USA.

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http://dx.doi.org/10.1159/000058376DOI Listing
October 2002