Works matching IS 00034800 AND DT 2015 AND VI 79 AND IP 2
Results: 7
A Clinical and Molecular Analysis of Branchio-Oculo-Facial Syndrome Patients in Russia Revealed New Mutations in TFAP2A.
- Published in:
- Annals of Human Genetics, 2015, v. 79, n. 2, p. 148, doi. 10.1111/ahg.12098
- By:
- Publication type:
- Article
Addressing Population-Specific Multiple Testing Burdens in Genetic Association Studies.
- Published in:
- Annals of Human Genetics, 2015, v. 79, n. 2, p. 136, doi. 10.1111/ahg.12095
- By:
- Publication type:
- Article
Effectiveness of Shrinkage and Variable Selection Methods for the Prediction of Complex Human Traits using Data from Distantly Related Individuals.
- Published in:
- Annals of Human Genetics, 2015, v. 79, n. 2, p. 122, doi. 10.1111/ahg.12099
- By:
- Publication type:
- Article
Admixed Origin of the Kayah (Red Karen) in Northern Thailand Revealed by Biparental and Paternal Markers.
- Published in:
- Annals of Human Genetics, 2015, v. 79, n. 2, p. 108, doi. 10.1111/ahg.12100
- By:
- Publication type:
- Article
Asp58Ala is the Predominant Mutation of the TTR Gene in Korean Patients with Hereditary Transthyretin-Related Amyloidosis.
- Published in:
- Annals of Human Genetics, 2015, v. 79, n. 2, p. 99, doi. 10.1111/ahg.12101
- By:
- Publication type:
- Article
A Novel Homozygous Nonsense Mutation in the PVRL4 Gene and Expansion of Clinical Spectrum of EDSS1.
- Published in:
- Annals of Human Genetics, 2015, v. 79, n. 2, p. 92, doi. 10.1111/ahg.12094
- By:
- Publication type:
- Article
De Novo Mutations in the BMPR2 Gene in Patients with Heritable Pulmonary Arterial Hypertension.
- Published in:
- Annals of Human Genetics, 2015, v. 79, n. 2, p. 85, doi. 10.1111/ahg.12096
- By:
- Publication type:
- Article