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المؤلفون: M. van Geel, D. Marcus-Soekarman, M. Devies, Maaike Vreeburg, E.A. de Zwart-Storm, Ruud G. L. Nellen, M.A.M. van Steensel, M.I. Schouten
المصدر: American Journal of Medical Genetics Part A. :360-363
مصطلحات موضوعية: Adult, Pathology, medicine.medical_specialty, DNA Mutational Analysis, Hyperkeratosis, Limb Deformities, Congenital, Connexin, Oculodentodigital dysplasia, Biology, medicine.disease_cause, Genetics, medicine, Humans, Abnormalities, Multiple, Eye Abnormalities, Keratoderma, Genetics (clinical), Sequence Deletion, Mutation, integumentary system, Tooth Abnormalities, Keratosis, medicine.disease, Dyskeratosis, Phenotype, Palmoplantar keratoderma, Dysplasia, Connexin 43, Skin Abnormalities, Female, Syndactyly
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2دورية أكاديمية
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