Associated Papers
A novel MECOM variant associated with congenital amegakaryocytic thrombocytopenia and radioulnar synostosis.
Al-Abboh H et al.
Pediatric Blood & Cancer, 2022
A de novo heterozygous HOXA11 variant in a patient with mesomelic dysplasia with urogenital abnormalities.
Sezer A et al.
American Journal of Medical Genetics. Part A, 2022
Human HOX gene disorders.
Quinonez SC et al.
Molecular Genetics and Metabolism, 2014
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