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  1. Article

    Open Access

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

    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 car...

    Khouloud Rjiba, Hédia Ayech, Olfa Kraiem, Wafa Slimani in Molecular Cytogenetics (2021)