Literature DB >> 14098761

[APROPOS OF 7 CASES OF ECTODERMAL DYSPLASIA IN SUBJECTS OF THE FEMALE SEX, 6 OF THEM IN THE SAME FAMILY. GENETIC DISCUSSION].

R BERNARD, F GIRAUD, M ROUBY, M HARTUNG.   

Abstract

Entities:  

Keywords:  ECTODERMAL DEFECT, CONGENITAL; GENETICS, HUMAN; INFANT, NEWBORN

Mesh:

Year:  1963        PMID: 14098761

Source DB:  PubMed          Journal:  Arch Fr Pediatr        ISSN: 0003-9764


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  3 in total

1.  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

2.  X-linked anhidrotic ectodermal dysplasia with some unusual features.

Authors:  W M Settineri; F M Salzano; M J Fretas
Journal:  J Med Genet       Date:  1976-06       Impact factor: 6.318

3.  Anhidrotic ectodermal dysplasia as autosomal recessive trait in an inbred kindred.

Authors:  E Passarge; C T Nuzum; W K Schubert
Journal:  Humangenetik       Date:  1966
  3 in total

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