Prenatal diagnosis of herlitz junctional epidermolysis bullosa by amniocentesis-Reference-Cited by-同舟云学术

Prenatal diagnosis of herlitz junctional epidermolysis bullosa by amniocentesis

Published:1995-11 Issue:11 Volume:15 Page:1027-1034
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Marinkovich M. Peter,Meneguzzi Guerrino,Burgeson Robert E.,Blanchet-Bardon Claudine,Holbrook Karen A.,Smith Lynne T.,Christiano Angela M.,Ortonne Jean-Paul

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Reference23 articles.

1. Herlitz's junctional epidermolysis bullosa is linked to mutations in the gene (LAMC2) for the γ2 subunit of nicein/kalinin (LAMININ–5)

2. Herlitz junctional epidermolysis bullosa keratinocytes display heterogeneous defects of nicein/kalinin gene expression.

3. A new nomenclature for the laminins

4. Revised clinical and laboratory criteria for subtypes of inherited epidermolysis bullosa

5. (1971). Epidermolysis Bullosa: A Clinical, Genetic and Epidemiologic Study, Baltimore: The Johns Hopkins Press, 1–180.

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1. Retrospective evidence on outcomes and experiences of pregnancy and childbirth in epidermolysis bullosa in Australia and New Zealand;International Journal of Women's Dermatology;2017-03

2. Retrospective evidence on outcomes and experiences of pregnancy and childbirth in epidermolysis bullosa in Australia and New Zealand;International Journal of Women's Dermatology;2015-02

3. Laminin-10 is crucial for hair morphogenesis;The EMBO Journal;2003-05-15

4. Genetic reversion of inherited skin disorders;Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis;2002-11

5. Junctional epidermolysis bullosa gravis (Herlitz): diagnostic and genetic aspects;Journal of the European Academy of Dermatology and Venereology;2001-01