Novel IDS Variants Identified in Three Unrelated Pakistani Patients Affected with Mucopolysaccharidosis Type II (Hunter Syndrome).
- Published in:
- Human Heredity, 2019, v. 84, n. 6, p. 279, doi. 10.1159/000510065
- By:
- Publication type:
- Article
Works matching IS 00015652 AND DT 2019 AND VI 84 AND IP 6
Results: 7
1
2
A Bayesian Hierarchical Framework for Pathway Analysis in Genome-Wide Association Studies.
- Published in:
- Human Heredity, 2019, v. 84, n. 6, p. 240, doi. 10.1159/000508664
- By:
- Publication type:
- Article
3
Front & Back Matter.
- Published in:
- Human Heredity, 2019, v. 84, n. 6, p. 1, doi. 10.1159/000512996
- Publication type:
- Article
4
A Homozygous RAG1 Gene Mutation in a Case of Combined Immunodeficiency: Clinical, Molecular, and Computational Analysis.
- Published in:
- Human Heredity, 2019, v. 84, n. 6, p. 272, doi. 10.1159/000510062
- By:
- Publication type:
- Article
5
Contents Vol. 84, 2019.
- Published in:
- Human Heredity, 2019, v. 84, n. 6, p. I, doi. 10.1159/000512546
- Publication type:
- Article
6
The Role of miR-210 in the Biological System: A Current Overview.
- Published in:
- Human Heredity, 2019, v. 84, n. 6, p. 233, doi. 10.1159/000509280
- By:
- Publication type:
- Article
7
Power and Sample Size Calculations for Genetic Association Studies in the Presence of Genetic Model Misspecification.
- Published in:
- Human Heredity, 2019, v. 84, n. 6, p. 256, doi. 10.1159/000508558
- By:
- Publication type:
- Article