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Application of high-resolution array comparative genomic hybridization in children with unknown synd...

Application of high-resolution array comparative genomic hybridization in children with unknown synd...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1891087558

Application of high-resolution array comparative genomic hybridization in children with unknown syndromic microcephaly

About this item

Full title

Application of high-resolution array comparative genomic hybridization in children with unknown syndromic microcephaly

Publisher

New York: Nature Publishing Group US

Journal title

Pediatric research, 2017-08, Vol.82 (2), p.253-260

Language

English

Formats

Publication information

Publisher

New York: Nature Publishing Group US

More information

Scope and Contents

Contents

Backround
Microcephaly can either be isolated or it may coexist with other neurological entities and/or multiple congenital anomalies, known as syndromic microcephaly. Although many syndromic cases can be classified based on the characteristic phenotype, some others remain uncertain and require further investigation. The present study describes...

Alternative Titles

Full title

Application of high-resolution array comparative genomic hybridization in children with unknown syndromic microcephaly

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_1891087558

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1891087558

Other Identifiers

ISSN

0031-3998,1530-0447

E-ISSN

1530-0447

DOI

10.1038/pr.2017.65

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