[XYY syndrome and trisomy 21 (48, XYY, 21+). A phenotype showing a combined autosomal and gonosomal chromosome aberrations].
作者信息
Murken J D, Lippoldmüller E, Spiess H
出版信息
Monatsschr Kinderheilkd (1902). 1972 Nov;120(11):469-71.
PMID:4264493
Abstract
摘要
相似文献
1
[XYY syndrome and trisomy 21 (48, XYY, 21+). A phenotype showing a combined autosomal and gonosomal chromosome aberrations].[XYY综合征与21三体（48，XYY，21 +）。一种显示常染色体和性染色体联合畸变的表型]
Monatsschr Kinderheilkd (1902). 1972 Nov;120(11):469-71.
2
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XYY chromosomal complement, proven by fluorescence, in a child with trisomy 21:48,XYY,21+.通过荧光检测证实，一名21三体患儿存在XYY染色体组成：48,XYY,21+。
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Double trisomy as a mosaic. Case history (48, XYY, + 21/47,XY, +21) and survey of the literature of mixed autosomal-gonosomal trisomies.嵌合型双三体。病例报告（48，XYY，+21/47，XY，+21）及常染色体-性染色体混合三体文献综述
Acta Genet Med Gemellol (Roma). 1978;27:67-74. doi: 10.1017/s0001566000009521.
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48,XYY,+13 karyotype in a liveborn infant.一名活产婴儿的核型为48,XYY,+13 。
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[Congenital leukemia with chromosome aberrations (Trisomy G) in a non-mongoloid child].
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Testicular agenesis in a boy with XY-XYY mosaicism.一名患有XY-XYY嵌合体的男孩的睾丸发育不全。
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