High Y-chromosomal Differentiation Among Ethnic Groups of Dir and Swat Districts, Pakistan.
- Published in:
- Annals of Human Genetics, 2017, v. 81, n. 6, p. 234, doi. 10.1111/ahg.12204
- By:
- Publication type:
- Article
Works matching IS 00034800 AND DT 2017 AND VI 81 AND IP 6
Results: 7
1
2
The Impact of FOXP3 Polymorphism on the Risk of Allergic Rhinitis: A Meta-Analysis.
- Published in:
- Annals of Human Genetics, 2017, v. 81, n. 6, p. 284, doi. 10.1111/ahg.12205
- By:
- Publication type:
- Article
3
Disease-Causing Variants in the ATL1 Gene Are a Rare Cause of Hereditary Spastic Paraplegia among Czech Patients.
- Published in:
- Annals of Human Genetics, 2017, v. 81, n. 6, p. 249, doi. 10.1111/ahg.12206
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- Publication type:
- Article
4
Prevalence of Mutations in Deafness-Causing Genes in Cochlear Implanted Patients with Profound Nonsyndromic Sensorineural Hearing Loss in Shandong Province, China.
- Published in:
- Annals of Human Genetics, 2017, v. 81, n. 6, p. 258, doi. 10.1111/ahg.12207
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- Publication type:
- Article
5
Ancestry Informative Marker Panel to Estimate Population Stratification Using Genome-wide Human Array.
- Published in:
- Annals of Human Genetics, 2017, v. 81, n. 6, p. 225, doi. 10.1111/ahg.12208
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- Publication type:
- Article
6
Interaction Between Val158Met Catechol-O-Methyltransferase Polymorphism and Social Cognitive Functioning in Schizophrenia: Pilot Study.
- Published in:
- Annals of Human Genetics, 2017, v. 81, n. 6, p. 267, doi. 10.1111/ahg.12209
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- Publication type:
- Article
7
Evaluation of CCAAT/Enhancer Binding Protein (C/EBP) Alpha (CEBPA) and Runt-Related Transcription Factor 1 (RUNX1) Expression in Patients with De Novo Acute Myeloid Leukemia.
- Published in:
- Annals of Human Genetics, 2017, v. 81, n. 6, p. 276, doi. 10.1111/ahg.12210
- By:
- Publication type:
- Article