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7q间质性缺失及β-葡萄糖醛酸酶基因排除定位的总结

A summary of 7q interstitial deletions and exclusion mapping of the gene for beta-glucuronidase.

作者信息

Fagan K, Gill A, Henry R, Wilkinson I, Carey B

机构信息

Department of Neonatology, Mater Hospital, Waratah, NSW 2298, Australia.

出版信息

J Med Genet. 1989 Oct;26(10):619-25. doi: 10.1136/jmg.26.10.619.

Abstract

Three patients are described with different phenotypes and differing de novo interstitial deletions of the long arm of a chromosome 7. The first patient has a deletion with loss of the proximal 7q11.23 band. Only three other cases have been reported with this particular deletion. Our second case shows mild dysmorphism similar to the other four patients reported with deletion of bands 7q21.12----21.3. Our third patient has a deletion of the 7q22.1----32.2 segment and has many of the phenotypic features of the other reported cases of del 7q22----32. GUSB, the gene for beta-glucuronidase, has been localised to the 7cen----q22 region. Analysis of beta-glucuronidase levels in blood leucocytes of our patients has helped more precisely to assign this gene locus to 7q21.11 or 7q22.1.

摘要

本文描述了3例具有不同表型且7号染色体长臂存在不同新发间质性缺失的患者。首例患者的缺失累及近端7q11.23带。仅有另外3例报道有这种特定的缺失。我们的第二例患者表现出轻度畸形,与另外4例报道的7q21.12----21.3带缺失患者相似。我们的第三例患者缺失7q22.1----32.2节段,具有其他报道的7q22----32缺失病例的许多表型特征。β-葡萄糖醛酸酶基因(GUSB)已定位于7cen----q22区域。对我们患者血液白细胞中β-葡萄糖醛酸酶水平的分析有助于更精确地将该基因座定位于7q21.11或7q22.1。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e25/1015712/5a7066e77087/jmedgene00060-0012-a.jpg

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