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Human Heredity|January 1, 1987
The sequence of chromosome 3 loci AHSG:TF:CHE1T Zelinski, H Kaita, M Lewis, et al.Human Heredity|June 30, 2021
Putative Digenic GJB2/MYO7A Inheritance of Hearing Loss Detected in a Patient with 48,XXYY Klinefelter SyndromeQin Zhang, Tiantian Qin, Wenmu Hu, et al.Human Heredity|January 1, 1987
Genetic studies of low-abundance human plasma proteins. IV. Improved typing of alpha-1 acid glycoprotein (orosomucoid) by isoelectric focusing and immunoblottingM H Escallon, R E Ferrell, M I KambohHuman Heredity|January 1, 1988
Gc subtypes in Finns, Swedes and Swedish LappsL Beckman, G Beckman, P O NylanderHuman Heredity|January 1, 1988
Study of possible genetic predisposition to endemic goitre among the Fur and Baggara tribes of the SudanR A Bayoumi, T S Taha, N SahaHuman Heredity|January 1, 1987
Distribution of alpha-1-antitrypsin and haptoglobin phenotypes in bladder cancer patientsH G Benkmann, H P Hanssen, R Ovenbeck, et al.Human Heredity|January 1, 1987
Serum protein markers in ankylosing spondylitisS Rantapää Dahlqvist, L BeckmanHuman Heredity|January 1, 1987
Genetic markers in patients with intracranial aneurysmsO Norrgård, G Beckman, L Beckman, et al.Human Heredity|October 31, 2022
Reduction of Missed Diagnosis of G6PD Deficiency in Heterozygous Females by G6PD/6PGD Ratio Assay Combined with Amplification Refractory Mutation System PCRShiguo Chen, Jian Gao, Qunyan Wu, et al.Pageof 237