Evidence for a recurrent microdeletion at chromosome...

Evidence for a recurrent microdeletion at chromosome 16p11.2 associated with congenital anomalies of the kidney and urinary tract (CAKUT) and Hirschsprung disease

Matthew G. Sampson, Curtis R. Coughlin II, Paige Kaplan, Laura K. Conlin, Kevin E.C. Meyers, Elaine H. Zackai, Nancy B. Spinner, Lawrence Copelovitch
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Volume:
152A
Year:
2010
Language:
english
Pages:
5
DOI:
10.1002/ajmg.a.33628
File:
PDF, 144 KB
english, 2010
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