Journal of Genetic Medicine : eISSN 2383-8442 / pISSN 1226-1769

Fig. 2.

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Fig. 2. The phenotypic spectrum of Cornelia de Lange syndrome according to the affected gene. In each affected gene, the mode of inheritance and sex ratio of patients are indicated. M, male; F, female; AD, autosomal dominant; XL, X-linked.
Journal of Genetic Medicine 2022;19:85-93 https://doi.org/10.5734/JGM.2022.19.2.85
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