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You searched for: Author/Creator Wu, Yaning

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1. A de novo interstitial deletion of 7q31.2q31.31 identified in a girl with developmental delay and hearing loss. Issue 2 (13th April 2016)

5. Clinical, developmental and molecular update on Cornelia de Lange syndrome and the cohesin complex: Abstracts from the 2014 Scientific and Educational Symposium. (21st April 2015)

6. Compound heterozygote CDK5RAP2 mutations in a Guatemalan/Honduran child with autosomal recessive primary microcephaly, failure to thrive and speech delay. (21st April 2015)

8. Hearing loss, coloboma and left ventricular enlargement in a boy with an interstitial 10q26 deletion. Issue 2 (29th April 2016)