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新的与X染色体连锁的智力迟钝、男性乳房发育和肥胖综合征与DXS255相关。

New X-linked syndrome of mental retardation, gynecomastia, and obesity is linked to DXS255.

作者信息

Wilson M, Mulley J, Gedeon A, Robinson H, Turner G

机构信息

Department of Medical Genetics, Prince of Wales Children's Hospital, Randwick, Sydney, Australia.

出版信息

Am J Med Genet. 1991 Sep 15;40(4):406-13. doi: 10.1002/ajmg.1320400405.

Abstract

We describe 14 males from 3 successive generations in a family who have X-linked mental retardation (XLMR), obesity, gynecomastia, speech difficulties, emotional lability, tapering fingers, and small feet. Linkage analysis using markers spread along the X chromosome demonstrated a gene localisation close to the centromere. Maximum lod scores for markers near the centromere, all at theta = 0.00, were 1.36 for DXS72, and 1.46 for DXYS1. The closest flanking markers which showed recombination were DXS84 and DXS94, defining the physical localisation within Xp21.1-q22. DXS255 was fully informative with lod-1 confidence interval for theta of 0.00-0.12. Clinical findings and linkage data in this family distinguish it from the Börjeson-Forssman-Lehmann syndrome and other previously described XLMR syndromes.

摘要

我们描述了一个家族中连续三代的14名男性,他们患有X连锁智力迟钝(XLMR)、肥胖、男性乳房发育、言语困难、情绪不稳定、手指变细和脚小。使用沿X染色体分布的标记进行连锁分析表明,有一个基因定位于靠近着丝粒的位置。着丝粒附近标记的最大对数优势分数,在θ = 0.00时,DXS72为1.36,DXYS1为1.46。显示重组的最紧密侧翼标记是DXS84和DXS94,确定了其物理定位在Xp21.1-q22内。DXS255在θ为0.00-0.12时具有完全信息性,对数优势置信区间为-1。该家族的临床发现和连锁数据将其与Börjeson-Forssman-Lehmann综合征及其他先前描述的XLMR综合征区分开来。

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