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Human Heredity
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June 16, 2024
A Statistical Testing Strategy Accounting for Random and Nonrandom (Skewed) X-Chromosome Inactivation Identifies Lung Cancer Susceptibility Loci among Smokers
Rodolphe 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 Ataxia
Senmao 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 Deafness
Amale 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 Diseases
Karishma Mahtani, Diana Park, Jessica Abbott, et al.
Human Heredity
|
January 1, 1985
Red cell NADH diaphorase variants in Japanese
K Shimizu, H Keino, A Mizutani, et al.
Human Heredity
|
January 1, 1987
Mitochondrial malic enzyme in human leukocytes
G Siebert, A Amorim
Human Heredity
|
January 1, 1987
Polymorphism of S-adenosylhomocysteine hydrolase in Italy
R 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 Punjab
S M Chahal, I J Bansal, I K Sehgal, et al.
Human Heredity
|
January 1, 1987
The association of Hp 1 and sickle cell disease
R S Ostrowski, J C Travis, E S Talley
Human Heredity
|
January 1, 1987
Method for the typing of the C3 polymorphism in stored sera by means of isoelectric focusing
G Beckman, C Sikström
Page
of 237
Search research articles
Search
Showing results (491-500 of 2,367) with videos related to
Sort By:
Page
of 237
Human Heredity
|
June 16, 2024
A Statistical Testing Strategy Accounting for Random and Nonrandom (Skewed) X-Chromosome Inactivation Identifies Lung Cancer Susceptibility Loci among Smokers
Rodolphe 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 Ataxia
Senmao 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 Deafness
Amale 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 Diseases
Karishma Mahtani, Diana Park, Jessica Abbott, et al.
Human Heredity
|
January 1, 1985
Red cell NADH diaphorase variants in Japanese
K Shimizu, H Keino, A Mizutani, et al.
Human Heredity
|
January 1, 1987
Mitochondrial malic enzyme in human leukocytes
G Siebert, A Amorim
Human Heredity
|
January 1, 1987
Polymorphism of S-adenosylhomocysteine hydrolase in Italy
R 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 Punjab
S M Chahal, I J Bansal, I K Sehgal, et al.
Human Heredity
|
January 1, 1987
The association of Hp 1 and sickle cell disease
R S Ostrowski, J C Travis, E S Talley
Human Heredity
|
January 1, 1987
Method for the typing of the C3 polymorphism in stored sera by means of isoelectric focusing
G Beckman, C Sikström
Page
of 237