Wikidata

(Q50307028)

English

Broadening the phenotype associated with mutations in UPF3B: two further cases with renal dysplasia and variable developmental delay.

scientific article published on 25 April 2012

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Statements

title
Broadening the phenotype associated with mutations in UPF3B: two further cases with renal dysplasia and variable developmental delay. (English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
22609145
retrieved
2 March 2018
reference URL
http://europepmc.org/abstract/MED/22609145

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