Literature DB >> 13030490

Congenital familial testicular deficiency.

A R SOHVAL, L J SOFFER.   

Abstract

Entities:  

Keywords:  EUNUCHOIDISM

Mesh：

Year:  1953        PMID： 13030490     DOI： 10.1016/0002-9343(53)90044-8

Source DB:  PubMed          Journal:  Am J Med        ISSN： 0002-9343            Impact factor:   4.965


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  7 in total

Review 1.  [ON THE CLINICAL ASPECTS AND HISTOPATHOLOGY OF PRIMARY MALE HYPOGONADISM. 1. NOSOLOGICAL CLASSIFICATION OF MALE HYPOGONADISM].

Authors:  O HORNSTEIN
Journal:  Arch Klin Exp Dermatol       Date:  1963-09-02

2.  Male hypogonadal syndromes.

Authors:  G I SWYER
Journal:  Proc R Soc Med       Date:  1954-06

3.  Localization of the gene for a syndrome of X-linked skeletal dysplasia and mental retardation to Xq27-qter.

Authors:  S R Dlouhy; J C Christian; J L Haines; P M Conneally; M E Hodes
Journal:  Hum Genet       Date:  1987-02       Impact factor: 4.132

4.  [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

5.  Undescended testes: treatment with gonadotropin.

Authors:  J R Bierich
Journal:  Eur J Pediatr       Date:  1982-12       Impact factor: 3.183

6.  A syndrome of hypogonadism, alopecia, diabetes mellitus, mental retardation, deafness, and ECG abnormalities.

Authors:  N J Woodhouse; N A Sakati
Journal:  J Med Genet       Date:  1983-06       Impact factor: 6.318

7.  Hypergonadotropic hypogonadism, progressive early-onset spinocerebellar ataxia, and late-onset sensorineural hearing loss: case report and literature review.

Authors:  E Sarikaya; Cg Ensert; Hc Gulerman
Journal:  Balkan J Med Genet       Date:  2011-12       Impact factor: 0.519
  7 in total

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