Prenatal diagnosis for keratin mutations to exclude transmission of epidermolytic hyperkeratosis

Rothnagel, J. A., Lin, M. T. S., Longley, M. A., Holder, R. A., Hazen, P. G., Levy, M. L. and Roop, D. R. (1998) Prenatal diagnosis for keratin mutations to exclude transmission of epidermolytic hyperkeratosis. Prenatal Diagnosis, 18 8: 826-830. doi:10.1002/(SICI)1097-0223(199808)18:8<826::AID-PD360>3.0.CO;2-5


Author Rothnagel, J. A.
Lin, M. T. S.
Longley, M. A.
Holder, R. A.
Hazen, P. G.
Levy, M. L.
Roop, D. R.
Title Prenatal diagnosis for keratin mutations to exclude transmission of epidermolytic hyperkeratosis
Journal name Prenatal Diagnosis   Check publisher's open access policy
ISSN 0197-3851
Publication date 1998-08
Sub-type Article (original research)
DOI 10.1002/(SICI)1097-0223(199808)18:8<826::AID-PD360>3.0.CO;2-5
Volume 18
Issue 8
Start page 826
End page 830
Total pages 5
Language eng
Keyword intermediate filaments
disease
genetics
mosaicism
Bullous Ichthyosiform Erythroderma
Palmoplantar Keratoderma
Lethal Genes
Mosaicism
Skin
Differentiation
Manifestation
Vorner
Nevus
Q-Index Code C1
Q-Index Status Provisional Code
Institutional Status Unknown

Document type: Journal Article
Sub-type: Article (original research)
Collection: School of Chemistry and Molecular Biosciences
 
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