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Journal of the American Academy of Dermatology|January 1, 1988
Palmar-plantar keratoderma. A clinical, ultrastructural, and biochemical studyV P Sybert, B A Dale, K A HolbrookThe Journal of Pediatrics|April 1, 1990
Pigmentary abnormalities and mosaicism for chromosomal aberration: association with clinical features similar to hypomelanosis of ItoV P Sybert, R A Pagon, M Donlan, et al.The Journal of Investigative Dermatology|May 1, 1987
Keratinocytes cultured from subjects with ichthyosis vulgaris are phenotypically abnormalP Fleckman, K A Holbrook, B A Dale, et al.The Journal of Investigative Dermatology|April 1, 1983
Epidermolytic hyperkeratosis: ultrastructure and biochemistry of skin and amniotic fluid cells from two affected fetuses and a newborn infantK A Holbrook, B A Dale, V P Sybert, et al.The Journal of Investigative Dermatology|August 1, 1993
A keratin 14 mutational hot spot for epidermolysis bullosa simplex, Dowling-Meara: implications for diagnosisK Stephens, V P Sybert, E M Wijsman, et al.The Journal of Investigative Dermatology|March 1, 1997
Primers for exon-specific amplification of the KRT5 gene: identification of novel and recurrent mutations in epidermolysis bullosa simplex patientsK Stephens, P Ehrlich, M Weaver, et al.Human Molecular Genetics|December 10, 1999
NF1 microdeletion breakpoints are clustered at flanking repetitive sequencesM O Dorschner, V P Sybert, M Weaver, et al.The New England Journal of Medicine|September 8, 1983
Evaluation of a protocol for post-mortem examination of stillbirthsR F Mueller, V P Sybert, J Johnson, et al.The Journal of Pediatrics|September 1, 1996
Prevalence of hypopigmented macules in a healthy populationS L Vanderhooft, J S Francis, R A Pagon, et al.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.Pageof 30