PARTIAL TRISOMY-17Q - KARYOTYPE - 46,XY,DER(21),T(17-21)(Q22-P13)

被引：20

作者：

FRYNS, JP

PARLOIR, C

VANDENBERGHE, H

机构：

[1] Division of Human Genetics, Department of Human Biology, Leuven, B-3000, Minderbroedersstraat

来源：

HUMAN GENETICS | 1979年 / 49卷 / 03期

关键词：

D O I：

10.1007/BF00569357

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

A 15-year-old deeply mentally retarded male is described with partial distal 17q trisomy (17q22→17qter), as the result of a de novo 17q/21p translocation. Differential Ag-staining showed that the satellites of chromosome 21 were included in the translocation chromosome. © 1979 Springer-Verlag.

引用

页码：361 / 364

页数：4

共 6 条

[1]

BIEDERMAN B, 1977, CLIN GENET, V11, P77

[2]

EIBERG H, 1974, LANCET, V2, P836

[3]

LATTA E, 1974, HUMANGENETIK, V23, P213

[4] INCLUSION OF SATELLITES IN AN 18-21 TRANSLOCATIONS CHROMOSOME SHOWN BY AMMONIACAL SILVER STAINING (SAT-BANDING) IN CASE OF PARTIAL TRISOMY-18 [J].

NEU, RL ;

ORTEGA, CC ;

BARG, GA ;

PINTO, W ;

GARDNER, LI ;

HOWELL, WM ;

DENTON, TE .

JOURNAL OF MEDICAL GENETICS, 1976, 13 (06) :520-522

[5]

PALUTKE W, 1976, CLIN GENET, V9, P454

[6]

SALMANCAGOMEZ F, 1975, ANN GENET, V18, P235

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