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一名患有X;Y易位的45,X男性:对特纳综合征和X连锁点状软骨发育不良相关基因定位的意义。

A 45,X male with an X;Y translocation: implications for the mapping of the genes responsible for Turner syndrome and X-linked chondrodysplasia punctata.

作者信息

Weil D, Portnoï M F, Levilliers J, Wang I, Mathieu M, Taillemite J L, Meier M, Boudailliez B, Petit C

机构信息

Institut Pasteur, Unité de Génétique Moléculaire Humaine (CNRS URA 1445), Paris, France.

出版信息

Hum Mol Genet. 1993 Nov;2(11):1853-6. doi: 10.1093/hmg/2.11.1853.

Abstract

In a male patient with a 45,X karyotype, the terminal part of the Y chromosome short arm was translocated as a single block on to the X chromosome. This rearranged X chromosome was, in every regard, the same as that present in XX males resulting from an abnormal X-Y interchange. Correlations between the phenotype of this patient and the extent of the deletions on the X and Y chromosomes allowed us to map the genes responsible for most features of the Turner syndrome between DXS432 and Xqter on the X chromosome, and the homologous Y genes either on Yp in interval 4 or on Yq. The molecular analysis of this X-Y translocation allowed us also to reduce the interval for the X-linked recessive chondrodysplasia punctata gene to a 1.5 Mb interval between DXS432 and DXS31.

摘要

在一名核型为45,X的男性患者中,Y染色体短臂的末端部分作为一个单一片段易位到了X染色体上。这条重排的X染色体在各方面都与因异常X-Y互换而产生的XX男性所携带的X染色体相同。该患者的表型与X和Y染色体上缺失范围之间的相关性,使我们能够将负责特纳综合征大多数特征的基因定位在X染色体上DXS432和Xqter之间,以及Y染色体上位于区间4的Yp或Yq上的同源Y基因。对这种X-Y易位的分子分析还使我们能够将X连锁隐性点状软骨发育不良基因的区间缩小到DXS432和DXS31之间1.5 Mb的区间。

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