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
Works matching IS 00034800 AND DT 2015 AND VI 79 AND IP 2
Results: 7
1
2
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
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- Publication type:
- Article
3
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
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- Publication type:
- Article
4
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
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- Publication type:
- Article
5
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
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- Publication type:
- Article
6
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
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- Publication type:
- Article
7
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