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对13例患有沃夫-贺许宏氏症候群[4号染色体短臂缺失(del(4p))]患者的基因与临床研究。

Genetic and clinical studies in 13 patients with the Wolf-Hirschhorn syndrome [del(4p)].

作者信息

Wilson M G, Towner J W, Coffin G S, Ebbin A J, Siris E, Brager P

出版信息

Hum Genet. 1981;59(4):297-307. doi: 10.1007/BF00295461.

Abstract

Clinical and cytogenetic studies are reported on 13 patients with Wolf-Hirschhorn syndrome. The oldest of the living twelve probands is 24 years of age. Three of these patients had a translocation involving the short arm of chromosome 4, and in one of these the anomalous chromosome was inherited from the father. Another three patients were believed, on the basis of GTG-staining, to have a translocation although the origin of the translocated chromatin could not be identified. In the remaining seven patients the anomalous chromosome appeared to be a simple deletion, although in two cases a translocation could not be ruled out. Cytogenetic studies in these patients suggest that the critical deletion involved in Wolf-Hirschhorn syndrome is within 4p16.

摘要

本文报告了13例Wolf-Hirschhorn综合征患者的临床和细胞遗传学研究情况。12名在世先证者中年龄最大的为24岁。其中3例患者存在涉及4号染色体短臂的易位,其中1例异常染色体来自父亲。另外3例患者,基于GTG染色,虽无法确定易位染色质的来源,但推测存在易位。其余7例患者,异常染色体似乎为单纯缺失,不过有2例不能排除易位情况。对这些患者的细胞遗传学研究表明,Wolf-Hirschhorn综合征所涉及的关键缺失位于4p16区域内。

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