Works matching IS 00034800 AND DT 2018 AND VI 82 AND IP 1
Results: 7
Evaluation of a Role for NPY and NPY2R in the Pathogenesis of Obesity by Mutation and Copy Number Variation Analysis in Obese Children and Adolescents.
- Published in:
- Annals of Human Genetics, 2018, v. 82, n. 1, p. 1, doi. 10.1111/ahg.12211
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- Publication type:
- Article
Construction of an Exome-Wide Risk Score for Schizophrenia Based on a Weighted Burden Test.
- Published in:
- Annals of Human Genetics, 2018, v. 82, n. 1, p. 11, doi. 10.1111/ahg.12212
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- Article
Exome Sequencing Identifies a Novel Nonsense Mutation of MYO6 as the Cause of Deafness in a Brazilian Family.
- Published in:
- Annals of Human Genetics, 2018, v. 82, n. 1, p. 23, doi. 10.1111/ahg.12213
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- Article
Issue Information.
- Published in:
- Annals of Human Genetics, 2018, v. 82, n. 1, p. 1, doi. 10.1111/ahg.12214
- Publication type:
- Article
Corrigendum.
- Published in:
- Annals of Human Genetics, 2018, v. 82, n. 1, p. 52, doi. 10.1111/ahg.12237
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- Article
Single-center experience of N-linked Congenital Disorders of Glycosylation with a Summary of Molecularly Characterized Cases in Arabs.
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- Annals of Human Genetics, 2018, v. 82, n. 1, p. 35, doi. 10.1111/ahg.12220
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- Article
Choledochal Cyst with 17q12 Chromosomal Duplication.
- Published in:
- Annals of Human Genetics, 2018, v. 82, n. 1, p. 48, doi. 10.1111/ahg.12221
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- Publication type:
- Article