Rare Diseases
Records 1 - 3 (of 3 Records) |
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A genotype and phenotype analysis of SMAD6 mutant patients with radioulnar synostosis. Shen Fang et al. Molecular genetics & genomic medicine 2021 e1850 |
Evaluation of Sporadic and Familial Cases with Craniofrontonasal Syndrome: A Wide Clinical Spectrum and Identification of a Novel EFNB1 Gene Mutation. Gürsoy Semra et al. Molecular syndromology 2021 12(5) 269-278 |
Clinical Genetics of Polydactyly: An Updated Review. Umair Muhammad et al. Frontiers in genetics 2018 9447 |