Report of a mother and daughter with the 12q14 microdeletion syndrome

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  • How to Cite this Article: Bibb AL, Rosenfeld JA, Weaver DD. 2012. Report of a mother and daughter with the 12q14 microdeletion syndrome. Am J Med Genet Part A 158A:417–422.

Abstract

The 12q14 microdeletion syndrome is characterized by microcephaly, short stature, osteopoikilosis, weight deficiency, and learning disabilities. We report on a mother and daughter with a 12q14 microdeletion. To our knowledge these are the first reported familial cases with the syndrome. We also discuss the genes in the deleted area that may be contributing to the phenotype. © 2011 Wiley Periodicals, Inc.

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