Literature DB >> 13212613

Anhidrotic hereditary ectodermal dysplasia; report of two cases in a brother and sister.

J B SEAGLE.   

Abstract

Entities:  

Keywords:  ECTODERMAL DYSPLASIA; SWEATING

Mesh:

Year:  1954        PMID: 13212613     DOI: 10.1016/s0022-3476(54)80264-2

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


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  5 in total

1.  Sex chromatin and gene action in the mammalian X-chromosome.

Authors:  M F LYON
Journal:  Am J Hum Genet       Date:  1962-06       Impact factor: 11.025

2.  Hypohidrotic ectodermal dysplasia in females. A critical analysis and argument for genetic heterogeneity.

Authors:  R J Gorlin; T Old; V E Anderson
Journal:  Z Kinderheilkd       Date:  1970

3.  A genetic study of anodontia in X-linked hypohidrotic ectodermal dysplasia.

Authors:  M Nakata; H Koshiba; K Eto; W E Nance
Journal:  Am J Hum Genet       Date:  1980-11       Impact factor: 11.025

4.  Gene effect in carriers of anhidrotic ectodermal dysplasia.

Authors:  C B Kerr; R S Wells; K E Cooper
Journal:  J Med Genet       Date:  1966-09       Impact factor: 6.318

5.  Ectodermal dysplasia associated with autoimmune disease.

Authors:  S O Hung; A Patterson
Journal:  Br J Ophthalmol       Date:  1984-05       Impact factor: 4.638

  5 in total

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