SANMATI CUDDAPAH to Female
This is a "connection" page, showing publications SANMATI CUDDAPAH has written about Female.
Connection Strength
0.060
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IRF6 Sequencing in Interrupted Clefting. Cleft Palate Craniofac J. 2016 05; 53(3):373-6.
Score: 0.019
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Expanding the phenotypic spectrum of ARCN1-related syndrome. Genet Med. 2022 06; 24(6):1227-1237.
Score: 0.008
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Bi-allelic variants in OGDHL cause a neurodevelopmental spectrum disease featuring epilepsy, hearing loss, visual impairment, and ataxia. Am J Hum Genet. 2021 12 02; 108(12):2368-2384.
Score: 0.007
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A new syndrome of moyamoya disease, kidney dysplasia, aminotransferase elevation, and skin disease associated with?de novo variants in RNF213. Am J Med Genet A. 2021 07; 185(7):2168-2174.
Score: 0.007
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De novo variants in MED12 cause X-linked syndromic neurodevelopmental disorders in 18 females. Genet Med. 2021 04; 23(4):645-652.
Score: 0.007
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Fetal cardiomyopathy in neurofibromatosis type I: Novel phenotype and review of the literature. Am J Med Genet A. 2019 06; 179(6):1042-1046.
Score: 0.006
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Efficacy of early treatment in patients with cobalamin C disease identified by newborn screening: a 16-year experience. Genet Med. 2017 08; 19(8):926-935.
Score: 0.005