Cri-du-chat Syndrome in a child with a 46,XX,der(5),t(4;5)(q32;p14)pat karyotype

AlanMcDermott; RayPoulding; DesmondCreery

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Cri-du-chat Syndrome in a child with a 46,XX,der(5),t(4;5)(q32;p14)pat karyotype

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An infant with the clinical features of Cri-du-chat Syndrome was found to possess one component of a subtle reciprocal translocation found in the father and identified as 46,XY,t(4;5)(q32;p14).

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《Human Genetics》 |1977年第1期|109-112|共页
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AlanMcDermott; RayPoulding; DesmondCreery;
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Southmead Hospital;

Cheltenham General Hospital;

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正文语种英语
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1. A Child with Multiple Congenital Malformations and a 46,XX,t(Bq+;Dq#x2212;)/45,XX,#x2212;B, #x2212;D, + der(B),t(Bq+;Dq#x2212;) Karyotype [J] . AlessandraCarnevale, Luis De LosCobos journal of medical genetics . 1973,第4期

机译：A Child with Multiple Congenital Malformations and a 46,XX,t(Bq+;Dq#x2212;)/45,XX,#x2212;B, #x2212;D, + der(B),t(Bq+;Dq#x2212;) Karyotype
2. Combined trisomy 9 and Ullrich-Turner syndrome in a girl with a 46,X,der(9)t(X;9)(q12;q32) karyotype [J] . Canun S, Mutchinick O, Shaffer LGFernandez C american journal of medical genetics . 1998,第3期

机译：Combined trisomy 9 and Ullrich-Turner syndrome in a girl with a 46,X,der(9)t(X;9)(q12;q32) karyotype
3. A 45, XX,5–,13–, dic+ karyotype in a case of cri-du-chat syndrome [J] . E. Niebuhr cytogenetic and genome research . 1972,第3期

机译：A 45, XX,5–,13–, dic+ karyotype in a case of cri-du-chat syndrome
4. Partial trisomy 6p: 46XX -10 der(10)t(6;10) (p22;q26)pat and HLA localisation. [O] . P Ferrando, C San Román, S Rodriguez de Cordoba, 1981

机译：部分三体性6p：46XX-10der（10）t（6; 10）（p22; q26）pat和HLA定位。
5. Partial trisomy 6p: 46,XX, -10, der(10),t(6;10) (p22;q26)pat and HLA localisation. [O] . Ferrando, P, San Román, C, Rodriguez de Cordoba, S, 1981

机译：部分三体性6p：46，XX，-10，der（10），t（6; 10）（p22; q26）pat和HLA定位。

Cri-du-chat Syndrome in a child with a 46,XX,der(5),t(4;5)(q32;p14)pat karyotype

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