06-P029 Congenital hypertelorism & osteopenia, a novel autosomal recessive disease of development

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06-P029 Congenital hypertelorism & osteopenia, a novel autosomal recessive disease of development

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Identification of a Novel Intragenic Deletion of the PHKD1 Gene in a Patient with Autosomal Recessive Polycystic Kidney Disease

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ژورنال

عنوان ژورنال: Mechanisms of Development

سال: 2009

ISSN: 0925-4773

DOI: 10.1016/j.mod.2009.06.255