Literature DB >> 13834605

Testicular feminisation and colour-blindness.

J S STEWART.   

Abstract

Entities:  

Keywords:  COLOR BLINDNESS/case reports; HERMAPHRODITISM/case reports

Mesh：

Year:  1959        PMID： 13834605     DOI： 10.1016/s0140-6736(59)91695-2

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


× No keyword cloud information.
  7 in total

1.  [Chromosomal anomalies and the heredity of acquired color sense disorders].

Authors:  R G FREY
Journal:  Albrecht Von Graefes Arch Ophthalmol       Date:  1961

2.  A sex-linked recessive form of spastic paraplegia.

Authors:  A W JOHNSTON; V A McKUSICK
Journal:  Am J Hum Genet       Date:  1962-03       Impact factor: 11.025

3.  Locus on human X chromosome for dihydrotestosterone receptor and androgen insensitivity.

Authors:  W J Meyer; B R Migeon; C J Migeon
Journal:  Proc Natl Acad Sci U S A       Date:  1975-04       Impact factor: 11.205

4.  A Search for Ocular Anomalies in Persons with Abnormal Numbers of Sex Chromosomes.

Authors:  C McCulloch; W S Hunter
Journal:  Can Med Assoc J       Date:  1962-01-06       Impact factor: 8.262

5.  [Hard-to-classify forms of intersexuality. II. Familial male pseudohermaphroditism with lacking or supernumerary Y chromosome as mosaic].

Authors:  W Sachsse; H J Gilfrich; C Overzier
Journal:  Klin Wochenschr       Date:  1970-08-15

6.  [Intersex types which are difficult to classify. I. Familial masculine pseudohermaphroditism with disproportioned virilization and chromosomal aberration].

Authors:  W Sachsse; H J Gilfrich; C Overzier
Journal:  Klin Wochenschr       Date:  1970-03-15

7.  Genetical studies in testicular feminization syndrome.

Authors:  K Boczkowski
Journal:  J Med Genet       Date:  1968-09       Impact factor: 6.318
  7 in total

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