The X linked recessive form of XY gonadal dysgenesis with a high incidence of gonadal germ cell tumours: clinical and genetic studies.

Author:

Mann J R,Corkery J J,Fisher H J,Cameron A H,Mayerova A,Wolf U,Kennaugh A A,Woolley V

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference25 articles.

1. Mendelian inheritance in man;IMcKusick, V.A.

2. Familial syndrome of streak gonads and normal male karyotype in five phenotypic females;Espiner, E.A.; Veale, A.M.; Sands, V.E.; Fitzgerald, P.H.;N Engl J Med,1970

3. Gonadal dysgenesis in individuals with apparently normal chromosomal complements: tabulation of cases and compilation of genetic data;Simpson, J.L.; Christakos, A.C.; Horwith, M.; Silverman, F.S.;Birth Defects,1971

4. Genetically determined sexreversal in 46, XY humans;German, J.; Simpson, J.L.; Chaganti, R.S.K.; Summitt, R.L.; Reid, L.B.; Merkatz, JR;Science,1978

5. XY gonadal dysgenesis: genetic heterogeneity based upon clinical observations, H-Y antigen status and segregation analysis;Simpson, J.L.; Blagowidow, N.; Martin, A.O.;Hum Genet,1981

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