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February 4, 2002American Journal of Medical GeneticsOpen Access

“Mowat‐Wilson” syndrome with and without Hirschsprung disease is a distinct, recognizable multiple congenital anomalies‐mental retardation syndrome caused by mutations in the zinc finger homeo box 1B gene

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Authors

CZChristiane ZweierUniversity Hospital of BernBABeate AlbrechtMax Planck SocietyBMBeate MitullaKlinik für Psychosomatik

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Zweier et al. (2002) studied this question.

synapsesocial.com/papers/6a63ca67b1ac4c8fd1f2d5dehttps://doi.org/10.1002/ajmg.10226
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Also Consider

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  3. 3Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23.1998 · 273 citations
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