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Pamela Ehrlich

Observed name: P Ehrlich
Observed institution: University of Washington
OpenAlex ID: A5113498765
Deletions spanning the neurofibromatosis 1 gene: identification and phenotype of five patients.
1994 · L M Kayes, W Burke, et al. · PubMed Central · 210
Primers for Exon-Specific Amplification of the KRT5 Gene: Identification of Novel and Recurrent Mutations in Epidermolysis Bullosa Simplex Patients
1997 · Karen Stephens, Pamela Ehrlich, et al. · Journal of Investigative Dermatology · 74
A Keratin 14 Mutational Hot Spot for Epidermolysis Bullosa Simplex, Dowling-Meara: Implications for Diagnosis
1993 · Karen Stephens, Virginia P Syber, et al. · Journal of Investigative Dermatology · 73
Epidermolysis bullosa simplex: a keratin 5 mutation is a fully dominant allele in epidermal cytoskeleton function.
1995 · K Stephens, A Zlotogorski, et al. · PubMed Central · 54
A Common Keratin 5 Gene Mutation in Epidermolysis Bullosa Simplex–Weber-Cockayne
1995 · Pamela Ehrlich, Virginia P Sybert, et al. · Journal of Investigative Dermatology · 32
Identification of a common keratin 5 mutation in epidermolysis bullosa simplex-Weber-Cockayne
1994 · Pamela Ehrlich, Virginia P. Sybert, et al. · Journal of Investigative Dermatology · 1
A homozygous mutation in keratin 5 is a fully dominant allele responsible for epidermolysis bullosa simplex
1994 · Karen Stephens, Luke L. H. Smith, et al. · The American Journal of Human Genetics
Works count: 7
Citation count: 444
H-index: 5
I10-index: 5
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