SANMATI CUDDAPAH to Phenotype
This is a "connection" page, showing publications SANMATI CUDDAPAH has written about Phenotype.
Connection Strength
0.067
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Expanding the phenotypic spectrum of ARCN1-related syndrome. Genet Med. 2022 06; 24(6):1227-1237.
Score: 0.025
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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: 0.022
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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: 0.020