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3号染色体短臂的间质缺失。胎儿病理学检查及对位于3(p11----p14.2)区域的β-半乳糖苷酶-1(GLB-1)基因的排除。

Interstitial deletion of the short arm of chromosome 3. Fetal pathology and exclusion of the gene for beta-galactosidase-1 (GLB-1) from 3(p11----p14.2).

作者信息

Hertz J M, Coerdt W, Hahnemann N, Schwartz M

机构信息

Institute of Human Genetics, University of Aarhus, Denmark.

出版信息

Hum Genet. 1988 Aug;79(4):389-91. doi: 10.1007/BF00282185.

Abstract

A de novo interstitial deletion of the short arm of chromosome 3 was prenatally diagnosed in a male fetus, karyotype 46,XY,del(3)(pter----p14.2::p11----qter). The fetus had craniofacial dysmorphisms, a single transverse palmar crease, ulnar deviation in the wrists, cardiovascular anomalies, a slight ureteric dilatation and a mobile caecum. Our observations are compared with five other cases with interstitial deletion of the short arm of chromosome 3 to delineate further the proximal 3p deletion syndrome. The gene for beta-galactosidase-1 (GLB-1) has previously been assigned to chromosome 3(p21----q21). The absence of a gene dosis effect for GLB-1 in this study indicates exclusion of GLB-1 from 3(p11----p14.2).

摘要

一名男性胎儿被产前诊断出3号染色体短臂存在新发间质性缺失,核型为46,XY,del(3)(pter----p14.2::p11----qter)。该胎儿有颅面畸形、单一横向掌褶、手腕尺侧偏斜、心血管异常、轻度输尿管扩张和活动盲肠。我们将观察结果与其他5例3号染色体短臂间质性缺失的病例进行比较,以进一步明确近端3p缺失综合征。β-半乳糖苷酶-1(GLB-1)基因先前已定位到3号染色体(p21----q21)。本研究中GLB-1不存在基因剂量效应,表明GLB-1不在3号染色体(p11----p14.2)区域。

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