Literature DB >> 14409876

The occurrence of ectodermal dysplasia and corneal dysplasia in one family: an inquiry into the mode of inheritance.

A H KLINE, J B SIDBURY, C P RICHTER.   

Abstract

Entities:  

Keywords:  ABNORMALITIES/genetics

Mesh：

Year:  1959        PMID： 14409876     DOI： 10.1016/s0022-3476(59)80230-4

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


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  6 in total

1.  Cytogenetic findings in 89 cases of Turner's syndrome with abnormal karyotypes.

Authors:  W Schmid; E Naef; G Mürset; A Prader
Journal:  Humangenetik       Date:  1974

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.  Anhidrotic ectodermal dysplasia with frequent infections and amyloidosis.

Authors:  R A Clark; G S Omenn
Journal:  West J Med       Date:  1977-03

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

6.  Anhidrotic ectodermal dysplasia with lacrimal anomalies.

Authors:  G M Liakos
Journal:  Br J Ophthalmol       Date:  1979-07       Impact factor: 4.638
  6 in total

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