常染色体显性Axenfeld-Rieger异常定位于6p25。 - Suppr

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Autosomal dominant Axenfeld-Rieger anomaly maps to 6p25.

作者信息

Gould D B, Mears A J, Pearce W G, Walter M A

出版信息

Am J Hum Genet. 1997 Sep;61(3):765-8.

PMID:9326342

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1715932/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5568/1715932/57b105da2152/ajhg00009-0302-a.jpg

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The detection and estimation of linkage between the genes for elliptocytosis and the Rh blood type.椭圆形红细胞增多症基因与Rh血型之间连锁关系的检测与评估。

Am J Hum Genet. 1956 Jun;8(2):80-96.

Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome.与里格尔综合征相关的新型类双尾同源框转录因子基因RIEG的克隆与鉴定

Nat Genet. 1996 Dec;14(4):392-9. doi: 10.1038/ng1296-392.

Autosomal-dominant iridogoniodysgenesis and Axenfeld-Rieger syndrome are genetically distinct.常染色体显性虹膜角膜内皮发育异常和Axenfeld-Rieger综合征在遗传学上是不同的。

Ophthalmology. 1996 Nov;103(11):1907-15. doi: 10.1016/s0161-6420(96)30408-9.

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Am J Hum Genet. 1996 Dec;59(6):1321-7.

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Genetic heterogeneity in Rieger eye malformation.里格尔眼畸形的遗传异质性。

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