Characterisation of deletions of the ZFHX1B region and genotype-phenotype analysis in Mowat-Wilson syndrome.
Zweier, C.; Temple, I.K.; Beemer, F.; Zackai, E.; Lerman-Sagie, T.; Weschke, B.; Anderson, C.E.; Rauch, A.; Journal of Medical Genetics, 2003, vol. 40, issue 8, p 601, ISSN 00222593. ISBN 14686244.

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