MODY type 2 in Greig cephalopolysyndactyly syndrome (GCPS) as part of a contiguous gene deletion syndrome

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American Journal Of Medical Genetics Part A, Vol. 155, Iss. 10, 2011-10 ,pp. : 2469-2472

John Wiley & Sons Inc

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Evidence for a new contiguous gene syndrome, the chromosome 16p13.3 deletion syndrome alias severe Rubinstein–Taybi syndrome

By Bartsch Oliver   Rasi Sasan   Delicado Alicia   Dyack Sarah   Neumann Luitgard   Seemanová Eva   Volleth Marianne   Haaf Thomas   Kalscheuer Vera  

Human Genetics, Vol. 120, Iss. 2, 2006-09 ,pp. : 179-186

Springer Publishing Company

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Delineation of the clinically recognizable 17q22 contiguous gene deletion syndrome in a patient carrying the smallest microdeletion known to date

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3p14 deletion is a rare contiguous gene syndrome: Report of 2 new patients and an overview of 14 patients

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Three‐generation family with novel contiguous gene deletion on chromosome 2p22 associated with thoracic aortic aneurysm syndrome

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