Evidence for a recurrent microdeletion at chromosome 16p11.2 associated with congenital anomalies of the kidney and urinary tract (CAKUT) and Hirschsprung disease.
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| Description | scientific article published in October 2010 |
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author: Matthew G Sampson Curtis R Coughlin Ii Lawrence Copelovitch |
| Publication date | October 1, 2010 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |