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The Journal of Investigative Dermatology|November 1, 1994
Hypomelanosis of Ito: a description, not a diagnosisV P Sybert
Human Genetics|January 1, 1992
Preferential mutation of the neurofibromatosis type 1 gene in paternally derived chromosomesK Stephens, L Kayes, V M Riccardi, et al.
American Journal of Human Genetics|March 1, 1995
Epidermolysis bullosa simplex: a keratin 5 mutation is a fully dominant allele in epidermal cytoskeleton functionK Stephens, A Zlotogorski, L Smith, et al.
The Journal of Investigative Dermatology|June 16, 2001
Expression of a truncated keratin 5 may contribute to severe palmar--plantar hyperkeratosis in epidermolysis bullosa simplex patientsR J Livingston, V P Sybert, L T Smith, et al.
Pediatric Dermatology|September 1, 1986
Hereditary hypotrichosis and localized morphea: a new clinical entityP Kulin, V P Sybert
Dermatologic Clinics|January 1, 1987
Prenatal diagnosis and screeningV P Sybert, K A Holbrook
The Journal of Pediatrics|January 1, 1987
Rapp-Hodgkin ectodermal dysplasiaH W Schroeder, V P Sybert
Current Opinion in Pediatrics|August 16, 2000
Molecular genetics in pediatric dermatologyM A Parisi, V P Sybert
American Journal of Medical Genetics|October 1, 1988
Idiopathic extrahepatic biliary atresia: recurrence in sibs in two familiesM L Cunningham, V P Sybert
Clinical Genetics|May 1, 1991
Association of annular pancreas and duodenal obstruction--evidence for Mendelian inheritance?S K Hendricks, V P Sybert
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