Disorders of sex development in Wolf–Hirschhorn syndrome: a genotype–phenotype correlation and MSX1 as candidate gene

Disorders of sex development in Wolf–Hirschhorn syndrome: a genotype–phenotype correlation and MSX1 as candidate gene

Abstract Background Wolf–Hirschhorn (WHS) is a set of congenital physical anomalies and mental retardation associated with a partial deletion of the short arm of chromosome 4. To establish a genotype–phenotype correlation; we carried out a molecular cytogenetic analysis on two Tunisian WHS patients....

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Bibliographic Details
Main Authors: Khouloud Rjiba, Hédia Ayech, Olfa Kraiem, Wafa Slimani, Afef Jelloul, Imen Ben Hadj Hmida, Nabiha Mahdhaoui, Ali Saad, Soumaya Mougou-Zerelli
Format: Article
Language:English
Published: BMC 2021-02-01
Series:Molecular Cytogenetics
Subjects:
Hypospadias
Array CGH
FISH
Wolf–Hirschhorn syndrome
MSX1gene
Online Access:https://doi.org/10.1186/s13039-021-00531-8

Internet

https://doi.org/10.1186/s13039-021-00531-8

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