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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 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.
The Journal of Investigative Dermatology|May 1, 1995
A common keratin 5 gene mutation in epidermolysis bullosa simplex--Weber-CockayneP Ehrlich, V P Sybert, A Spencer, et al.
American Journal of Human Genetics|March 3, 1999
Cyclic ichthyosis with epidermolytic hyperkeratosis: A phenotype conferred by mutations in the 2B domain of keratin K1V P Sybert, J S Francis, L D Corden, 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.
Pediatrics|January 7, 1998
Cardiovascular malformations and complications in Turner syndromeV P Sybert
The Journal of Pediatrics|March 1, 1984
Adult height in Turner syndrome with and without androgen therapyV P Sybert
Pediatric Dermatology|June 1, 1989
Hypohidrotic ectodermal dysplasia: argument against an autosomal recessive form clinically indistinguishable from X-linked hypohidrotic ectodermal dysplasia (Christ-Siemens-Touraine syndrome)V P Sybert
Pediatric Dermatology|November 1, 1985
Aplasia cutis congenita: a report of 12 new families and review of the literatureV P Sybert
Archives of Dermatology|November 1, 1993
Principles of genetics in the molecular era. A primer for dermatologistsV P Sybert
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