Evidence for a recurrent microdeletion at chromosome 16p11.2 associated with congenital anomalies of the kidney and urinary tract (CAKUT) and Hirschsprung disease. (Q53303831)
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scientific article published in October 2010
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Evidence for a recurrent microdeletion at chromosome 16p11.2 associated with congenital anomalies of the kidney and urinary tract (CAKUT) and Hirschsprung disease. |
scientific article published in October 2010 |
Statements
Evidence for a recurrent microdeletion at chromosome 16p11.2 associated with congenital anomalies of the kidney and urinary tract (CAKUT) and Hirschsprung disease (English)
Paige Kaplan
Laura K Conlin
Kevin E C Meyers
Elaine H Zackai
Nancy B Spinner