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Human Heredity|June 16, 2024
A Statistical Testing Strategy Accounting for Random and Nonrandom (Skewed) X-Chromosome Inactivation Identifies Lung Cancer Susceptibility Loci among SmokersRodolphe Jantzen, Sophie Camilleri-Broët, Nicole Ezer, et al.Human Heredity|October 29, 2023
A Novel c.3636-4 A>G Mutation in the CCDC88C Plays a Causative Role in Familial Spinocerebellar AtaxiaSenmao Chai, Deyang Liu, Yajing Liu, et al.Human Heredity|December 5, 2019
Further Evidence for the Implication of the MET Gene in Non-Syndromic Autosomal Recessive DeafnessAmale Bousfiha, Zied Riahi, Lamiae Elkhattabi, et al.Human Heredity|October 27, 2021
Importance of Family History in the Era of Exome Analysis: A Report of a Family with Multiple Concurrent Genetic DiseasesKarishma Mahtani, Diana Park, Jessica Abbott, et al.Human Heredity|January 1, 1985
Red cell NADH diaphorase variants in JapaneseK Shimizu, H Keino, A Mizutani, et al.Human Heredity|January 1, 1987
Polymorphism of S-adenosylhomocysteine hydrolase in ItalyR M Corbo, R Palmarino, E Schiattarella, et al.Human Heredity|January 1, 1987
Electrophoretic variants of red cell phosphoglucose isomerase in some caste populations of PunjabS M Chahal, I J Bansal, I K Sehgal, et al.Human Heredity|January 1, 1987
The association of Hp 1 and sickle cell diseaseR S Ostrowski, J C Travis, E S TalleyHuman Heredity|January 1, 1987
Method for the typing of the C3 polymorphism in stored sera by means of isoelectric focusingG Beckman, C SikströmPageof 237