Prenatal Diagnosis and Molecular Cytogenetic Analyses of a de novo Deletion on Chromosome 4p16.3p15....
Prenatal Diagnosis and Molecular Cytogenetic Analyses of a de novo Deletion on Chromosome 4p16.3p15.33
About this item
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Author / Creator
Luo, Huili , Chang, Ruijie , Liu, Fangfang and Gao, Xia
Publisher
United States: InnoVision Health Media, Inc
Journal title
Language
English
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Publication information
Publisher
United States: InnoVision Health Media, Inc
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Scope and Contents
Contents
Wolf-Hirschhorn syndrome (WHS) (OMIM 194190) is a contiguous gene syndrome with an estimated prevalence of around 1 in 50,000 births. The syndrome is caused by the deletion of a critical region (Wolf-Hirschhorn Syndrome Critical region-WHSCR) on chromosome 4p16.3. Its core features are typical facial gestalt, growth retardation, intellectual disabi...
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Full title
Prenatal Diagnosis and Molecular Cytogenetic Analyses of a de novo Deletion on Chromosome 4p16.3p15.33
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Record Identifier
TN_cdi_proquest_miscellaneous_2865789026
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2865789026
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ISSN
1078-6791
