Log in to save to my catalogue
Log in to save to my catalogue

Prenatal Diagnosis of a 2.5 Mb De Novo 17q24.1q24.2 Deletion Encompassing KPNA2 and PSMD12 Genes in...

| Ask | Become a Library member

Prenatal Diagnosis of a 2.5 Mb De Novo 17q24.1q24.2 Deletion Encompassing KPNA2 and PSMD12 Genes in...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1894915826

Prenatal Diagnosis of a 2.5 Mb De Novo 17q24.1q24.2 Deletion Encompassing KPNA2 and PSMD12 Genes in a Fetus with Craniofacial Dysmorphism, Equinovarus Feet, and Syndactyly

About this item

Full title

Prenatal Diagnosis of a 2.5 Mb De Novo 17q24.1q24.2 Deletion Encompassing KPNA2 and PSMD12 Genes in a Fetus with Craniofacial Dysmorphism, Equinovarus Feet, and Syndactyly

Author / Creator

Naud, Marie-Emmanuelle , Tosca, Lucie , Martinovic, Jelena , Saada, Julien , Métay, Corinne , Drévillon, Loïc , Benoit, Virginie , Brisset, Sophie and Tachdjian, Gérard

Journal title

Case reports in genetics, 2017, Vol.2017, p.7803136-7803136

Language

English

Formats

Reports

More information

Alternative Titles

Full title

Prenatal Diagnosis of a 2.5 Mb De Novo 17q24.1q24.2 Deletion Encompassing KPNA2 and PSMD12 Genes in a Fetus with Craniofacial Dysmorphism, Equinovarus Feet, and Syndactyly

Authors, Artists and Contributors

Author / Creator

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_1894915826

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1894915826

Other Identifiers

ISSN

2090-6544

DOI

10.1155/2017/7803136

How to access this item

Log in as a Library member

Full text available

View in old catalogue

Connecting people and collections