ELIZABETH ROEDER to Heterozygote
This is a "connection" page, showing publications ELIZABETH ROEDER has written about Heterozygote.
Connection Strength
0.170
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De novo heterozygous mutations in SMC3 cause a range of Cornelia de Lange syndrome-overlapping phenotypes. Hum Mutat. 2015 Apr; 36(4):454-62.
Score: 0.098
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De novo heterozygous missense and loss-of-function variants in CDC42BPB are associated with a neurodevelopmental phenotype. Am J Med Genet A. 2020 05; 182(5):962-973.
Score: 0.034
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Autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants. Genet Med. 2018 10; 20(10):1175-1185.
Score: 0.030
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Familial paragangliomas: the emerging impact of molecular genetics on evaluation and management. Am J Otol. 1999 Sep; 20(5):639-43.
Score: 0.008