Log in to save to my catalogue

Wolf-Hirschhorn Syndrome: A Case with Normal Karyotype, Demonstrated by Array CGH (aCGH)

Wolf-Hirschhorn Syndrome: A Case with Normal Karyotype, Demonstrated by Array CGH (aCGH)

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_1562564662

Wolf-Hirschhorn Syndrome: A Case with Normal Karyotype, Demonstrated by Array CGH (aCGH)

About this item

Full title

Wolf-Hirschhorn Syndrome: A Case with Normal Karyotype, Demonstrated by Array CGH (aCGH)

Publisher

Tehran: Academy of Medical Sciences of I.R. Iran

Journal title

Archives of Iranian medicine, 2014-09, Vol.17 (9), p.642

Language

English

Formats

Publication information

Publisher

Tehran: Academy of Medical Sciences of I.R. Iran

More information

Scope and Contents

Contents

Wolf-Hirschhorn syndrome (WHS) is a disorder that affects many parts of the body. The major features of this condition include specific craniofacial malformations, delayed growth and development, intellectual disability and seizures. Here, we report a case of WHS: a 27-month-old girl with a microdeletion at distal part of short arm of chromosome 4....

Alternative Titles

Full title

Wolf-Hirschhorn Syndrome: A Case with Normal Karyotype, Demonstrated by Array CGH (aCGH)

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_journals_1562564662

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_1562564662

Other Identifiers

ISSN

1029-2977

E-ISSN

1735-3947

How to access this item