Characterisation of deletions of the ZFHX1B region and genotype-phenotype analysis in Mowat-Wilson syndrome.
作者信息
Zweier C, Temple I K, Beemer F, Zackai E, Lerman-Sagie T, Weschke B, Anderson C E, Rauch A
出版信息
J Med Genet. 2003 Aug;40(8):601-5. doi: 10.1136/jmg.40.8.601.
Abstract
摘要
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