Wikidata

(Q53303831)

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

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title
Evidence for a recurrent microdeletion at chromosome 16p11.2 associated with congenital anomalies of the kidney and urinary tract (CAKUT) and Hirschsprung disease (English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20799338
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20799338%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 February 2020

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