Cytogenetic and molecular diagnosis of Fanconi anemia revealed two hidden phenotypes: Disorder of sex development and cerebro‐oculo‐facio‐skeletal syndrome
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DOI: 10.1002/mgg3.694
Abstract: Several studies have shown a high rate of consanguinity and endogamy in North African populations. As a result, the frequency of autosomal recessive diseases is relatively high in the region with the co‐occurrence of two… read more here.
Keywords: fanconi anemia; diagnosis fanconi; anemia revealed; molecular diagnosis ... See more keywords