Naegeli-Franceschetti-Jadassohn Syndrome and Dermatopathia Pigmentosa Reticularis: Two Allelic Ectodermal Dysplasias Caused by Dominant Mutations in KRT14-Reference-Cited by-同舟云学术

Naegeli-Franceschetti-Jadassohn Syndrome and Dermatopathia Pigmentosa Reticularis: Two Allelic Ectodermal Dysplasias Caused by Dominant Mutations in KRT14

Published:2006-10 Issue:4 Volume:79 Page:724-730
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Lugassy Jennie,Itin Peter,Ishida-Yamamoto Akemi,Holland Kristen,Huson Susan,Geiger Dan,Hennies Hans Christian,Indelman Margarita,Bercovich Dani,Uitto Jouni,Bergman Reuven,McGrath John A.,Richard Gabriele,Sprecher Eli

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference41 articles.

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3. Dermatopathia pigmentosa reticularis: a report of a family demonstrating autosomal dominant inheritance;Heimer;J Am Acad Dermatol,1992

4. The gene for Naegeli-Franceschetti-Jadassohn syndrome maps to 17q21;Whittock;J Invest Dermatol,2000

5. Refined mapping of Naegeli-Franceschetti-Jadassohn syndrome to a 6 cM interval on chromosome 17q11.2-q21 and investigation of candidate genes;Sprecher;J Invest Dermatol,2002

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