Literature DB >> 13250193

Male pseudohermaphroditism: a hitherto undescribed form.

G I SWYER.   

Abstract

Entities:  

Keywords:  HERMAPHRODITISM

Mesh：

Year:  1955        PMID： 13250193      PMCID： PMC1980764          DOI： 10.1136/bmj.2.4941.709

Source DB:  PubMed          Journal:  Br Med J        ISSN： 0007-1447


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  7 in total

1.  The webbing syndrome (Ullrich-Turner) with and without gonadal agenesis: chromosomal sex typing by skin cell or leucocyte examination in diagnosis.

Authors:  A RUSSELL; B LEVIN; M WILMERS
Journal:  Proc R Soc Med       Date:  1955-04

2.  Chromosomal sex in ovarian agenesis.

Authors:  L WILKINS; M M GRUMBACH; J J VAN WYK
Journal:  J Clin Endocrinol Metab       Date:  1954-10       Impact factor: 5.958

3.  Chromosomal sex in Turner's syndrome with coarctation of the aorta.

Authors:  P E POLANI; W F HUNTER; B LENNOX
Journal:  Lancet       Date:  1954-07-17       Impact factor: 79.321

4.  The detection of chromosomal sex in hermaphrodites from a skin biopsy.

Authors:  K L MOORE; M A GRAHAM; M L BARR
Journal:  Surg Gynecol Obstet       Date:  1953-06

5.  Male pseudohermaphrodism.

Authors:  C N ARMSTRONG
Journal:  Proc R Soc Med       Date:  1953-04

6.  A case of male pseudohermaphroditism.

Authors:  D C BEATTY; C J CHAMP; G I M SWYER
Journal:  Br Med J       Date:  1953-06-20

7.  The hereditary occurrence of testes and absence of sexual hair in amenorrheic women: a type of pseudohermaphroditism.

Authors:  R W SCHNEIDER; R A VAN OMMEN; S O HOERR
Journal:  J Clin Endocrinol Metab       Date:  1952-04       Impact factor: 5.958
  7 in total
  31 in total

Review 1.  Etiopathogenesis, classification, investigations and diagnosis in intersex disorders.

Authors:  M G Forest
Journal:  Indian J Pediatr       Date:  1992 Jul-Aug       Impact factor: 1.967

2.  [CHROMOSOME MOSAIC 45/XO-/46XX-/47/XXX SIMULATING A "TRUE GONADAL DYSGENESIS"].

Authors:  R ZABEL; R WITKOWSKI; J DAMM
Journal:  Arch Klin Exp Dermatol       Date:  1964-05-15

3.  Goldberg-Maxwell syndrome; report of the anomaly in three sisters.

Authors:  R VAISH
Journal:  Br Med J       Date:  1958-12-06

4.  The chromosomes in a case of pure gonadal dysgenesis.

Authors:  D G HARNDEN; J S STEWART
Journal:  Br Med J       Date:  1959-12-12

5.  Gonadal dysgenesis in normal-looking females; a genetic theory to explain variability of the syndrome.

Authors:  R HOFFENBERG; W P JACKSON
Journal:  Br Med J       Date:  1957-06-01

6.  Nuclei and sex.

Authors:  W M DAVIDSON; D R SMITH
Journal:  Postgrad Med J       Date:  1956-12       Impact factor: 2.401

7.  Mutations in the conserved domain of SRY are uncommon in XY gonadal dysgenesis.

Authors:  E K Pivnick; S Wachtel; D Woods; J L Simpson; C E Bishop
Journal:  Hum Genet       Date:  1992-11       Impact factor: 4.132

8.  Pure gonadal dysgenesis (type XX). Report on a family with four affected sibs.

Authors:  H R Nazareth; L M Farah; A J Cunha; F J Vieira
Journal:  Hum Genet       Date:  1977-06-10       Impact factor: 4.132

9.  An extended long-range restriction map of the human sex-determining region on Yp, including ZFY, finds marked homology on Xp and no detectable Y sequences in an XX male.

Authors:  V Verga; R P Erickson
Journal:  Am J Hum Genet       Date:  1989-05       Impact factor: 11.025

10.  H-Y antigen in Swyer syndrome and the genetics of XY gonadal dysgenesis.

Authors:  C A Moreira-Filho; S P Toledo; V R Bagnolli; O Frota-Pessoa; H Bisi; A Wajntal
Journal:  Hum Genet       Date:  1979       Impact factor: 4.132
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