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

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. Patient...

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Detalles Bibliográficos
Autores principales: Rjiba, Khouloud, Ayech, Hédia, Kraiem, Olfa, Slimani, Wafa, Jelloul, Afef, Ben Hadj Hmida, Imen, Mahdhaoui, Nabiha, Saad, Ali, Mougou-Zerelli, Soumaya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7905666/
https://www.ncbi.nlm.nih.gov/pubmed/33627176
http://dx.doi.org/10.1186/s13039-021-00531-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7905666/
https://www.ncbi.nlm.nih.gov/pubmed/33627176
http://dx.doi.org/10.1186/s13039-021-00531-8

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