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一名患有X/Y易位的男童Xp远端部分出现零体。

Nullisomy for the distal portion of Xp in a male child with a X/Y translocation.

作者信息

Tiepolo L, Zuffardi O, Rodewald A

出版信息

Hum Genet. 1977 Dec 23;39(3):277-81. doi: 10.1007/BF00295420.

Abstract

An unbalanced X/Y translocation was found in a male child with malformed external genitalia and in his mother, who are respectively nullisomic and monosomic for the distal portion of Xp and have the translocated distal segment of Yq in excess. The loss of the distal portion of Xp is supposed to be the cause of the phenotypic abnormalities present in these subjects. The phenotype of our subjects is compared with those of the other cases of X/Y translocation described in the literature.

摘要

在一名患有外生殖器畸形的男童及其母亲体内发现了一种不平衡的X/Y易位。他们分别在Xp远端部分存在染色体缺失和单体性,并且多余地拥有Yq的易位远端片段。Xp远端部分的缺失被认为是这些受试者出现表型异常的原因。我们受试者的表型与文献中描述的其他X/Y易位病例的表型进行了比较。

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