Medical Pearl: An easy way to diagnose severe neonatal monilethrix-Reference-Cited by-同舟云学术

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Medical Pearl: An easy way to diagnose severe neonatal monilethrix

Published:2002-01 Issue:1 Volume:46 Page:111-112
ISSN:0190-9622
Container-title:Journal of the American Academy of Dermatology
language:en
Short-container-title:Journal of the American Academy of Dermatology

Author:

Landau Marina,Brenner Sarah,Metzker Aryeh

Publisher

Elsevier BV

Subject

Dermatology

Reference7 articles.

1. Pediatric dermatology;Schachner,1995

2. Identification of novel mutations in basic hair keratins hHb1 and hHb6 in monilethrix: implications for protein structure and clinical phenotype;Korge;J Invest Dermatol,1999

3. Monilethrix: mutational hotspot in the helix termination motif of the human hair basic keratin 6;Horev;Hum Hered,2000

4. Monilethrix: an ultrastructural study;Ito;J Cutan Pathol,1984

5. The genetic analysis of monilethrix in a large inbred kindred;Schaap;Am J Med Genet,1982

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3. 15 Diseases of cutaneous appendages;Weedon's Skin Pathology;2010

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