Characterisation of deletions of the ZFHX1B region and genotype-phenotype analysis in Mowat-Wilson syndrome

C. Zweier, I. K. Temple, F. Beemer, E. Zackai, T. Lerman-Sagie, B. Weschke, C. E. Anderson, A. Rauch

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)601-605
Number of pages5
JournalJournal of Medical Genetics
Issue number8
StatePublished - 1 Aug 2003
Externally publishedYes

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