Works matching IS 00034800 AND DT 2014 AND VI 78 AND IP 3
Results: 7
Complete Mitochondrial Genome Analysis and Clinical Documentation of a Five-Generational Indian Family with Mitochondrial 1555A>G Mutation and Postlingual Hearing Loss.
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- Annals of Human Genetics, 2014, v. 78, n. 3, p. 217, doi. 10.1111/ahg.12061
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Novel Variants in the MC4R and LEPR Genes among Severely Obese Children from the Iberian Population.
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- Annals of Human Genetics, 2014, v. 78, n. 3, p. 195, doi. 10.1111/ahg.12058
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Effective Variant Detection by Targeted Deep Sequencing of DNA Pools: An Example from Parkinson's Disease.
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- Annals of Human Genetics, 2014, v. 78, n. 3, p. 243, doi. 10.1111/ahg.12060
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- Article
Surnames in Honduras: A Study of the Population of Honduras through Isonymy.
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- Annals of Human Genetics, 2014, v. 78, n. 3, p. 165, doi. 10.1111/ahg.12057
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- Article
Maternal Genetic Heritage of Southeastern Europe Reveals a New Croatian Isolate and a Novel, Local Sub-Branching in the X2 Haplogroup.
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- Annals of Human Genetics, 2014, v. 78, n. 3, p. 178, doi. 10.1111/ahg.12056
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- Article
Update of the Spectrum of GJB2 Mutations in 107 Patients with Nonsyndromic Hearing Loss in the Fujian Population of China.
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- Annals of Human Genetics, 2014, v. 78, n. 3, p. 235, doi. 10.1111/ahg.12062
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- Article
Mutation Screening of the HGD Gene Identifies a Novel Alkaptonuria Mutation with Significant Founder Effect and High Prevalence.
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- Annals of Human Genetics, 2014, v. 78, n. 3, p. 155, doi. 10.1111/ahg.12055
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- Article