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letter . 2003 Aug;40(8):601–605. doi: 10.1136/jmg.40.8.601
Characterisation of deletions of the ZFHX1B region and genotype-phenotype analysis in Mowat-Wilson syndrome
C Zweier
, I Temple
, F Beemer
, E Zackai
, T Lerman-Sagie
, B Weschke
, C Anderson
, A Rauch
C Zweier
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I Temple
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F Beemer
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E Zackai
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T Lerman-Sagie
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B Weschke
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C Anderson
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A Rauch
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PMCID: PMC1735564 PMID: 12920073
See the article "Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23." in volume 35 on page 617.