Characterisation of deletions of the ZFHX1B region and genotype-phenotype analysis in Mowat-Wilson syndrome.
Zweier C; Temple IK; Beemer F; Zackai E; Lerman-Sagie T; Weschke B; Anderson CE; Rauch A; Journal Of Medical Genetics, 2003, vol. 40, issue 8, p 601, ISSN 14686244. ISBN 14686244.

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