A gene for universal congenital alopecia maps to chromosome 8p21-22 (Q24538720)

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S Cichon

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I R Vogt

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S Hemmer

4

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R Kruse

5

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M Knapp

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T Höller

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M Faiyaz ul Haque

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S Haque

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P Propping

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M Ahmad

American Journal of Human Genetics

11

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language of work or name

English

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publication date

February 1998

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published in

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volume

62

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issue

2

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page(s)

386-90

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Expression of a dominant negative mutant of epidermal growth factor receptor in the epidermis of transgenic mice elicits striking alterations in hair follicle development and skin structure

27 September 2017

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Atrichias and hypotrichoses: a brief review with description of a recessive atrichia in two brothers

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Heritable disorders of hair

27 September 2017

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Genetic disorders associated with severe alopecia in children: a report of two unusual cases and a review

27 September 2017

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27 September 2017

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X-linked recessive inheritance in a family with isolated congenital alopecia.

29 November 2018

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12 December 2020

[Atrichia congenita and its heredity]

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12 December 2020

Isolated congenital atrichia in an Omani kindred

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12 December 2020

A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13

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12 December 2020

[Total familial hereditary hypotrichosis in four generations.]

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12 December 2020

Identifiers

DOI

10.1086/301717

1 reference

1 reference

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PubMed publication ID

9463324

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