Genetic Analyses of a Three Generation Family Segregating Hirschsprung Disease and Iris Heterochromia.
We present the genetic analyses conducted on a three-generation family (14 individuals) with three members affected with isolated-Hirschsprung disease (HSCR) and one with HSCR and heterochromia iridum (syndromic-HSCR), a phenotype reminiscent of Waardenburg-Shah syndrome (WS4). WS4 is characterized...
Main Authors: | , , , , , , , , |
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格式: | 文件 |
语言: | English |
出版: |
Public Library of Science (PLoS)
2013-01-01
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丛编: | PLoS ONE |
在线阅读: | http://europepmc.org/articles/PMC3694150?pdf=render |