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Sequence variants of the HTR3A gene contribute to the genetic prediction of postoperative nausea in Taiwan.
- Published in:
- Journal of Human Genetics, 2014, v. 59, n. 12, p. 655, doi. 10.1038/jhg.2014.89
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- Article
Precise detection of chromosomal translocation or inversion breakpoints by whole-genome sequencing.
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- Journal of Human Genetics, 2014, v. 59, n. 12, p. 649, doi. 10.1038/jhg.2014.88
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- Article
Compound heterozygous BRAT1 mutations cause familial Ohtahara syndrome with hypertonia and microcephaly.
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- Journal of Human Genetics, 2014, v. 59, n. 12, p. 687, doi. 10.1038/jhg.2014.91
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- Article
A canonical splice site mutation in GIPC3 causes sensorineural hearing loss in a large Pakistani family.
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- Journal of Human Genetics, 2014, v. 59, n. 12, p. 683, doi. 10.1038/jhg.2014.86
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- Article
The somatic GNAQ mutation c.548G>A (p.R183Q) is consistently found in Sturge-Weber syndrome.
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- Journal of Human Genetics, 2014, v. 59, n. 12, p. 691, doi. 10.1038/jhg.2014.95
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- Article
Forensic STR loci reveal common genetic ancestry of the Thai-Malay Muslims and Thai Buddhists in the deep Southern region of Thailand.
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- Journal of Human Genetics, 2014, v. 59, n. 12, p. 675, doi. 10.1038/jhg.2014.93
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- Article
Identification of the rare compound heterozygous variants in the NEB gene in a Korean family with intellectual disability, epilepsy and early-childhood-onset generalized muscle weakness.
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- Journal of Human Genetics, 2014, v. 59, n. 12, p. 643, doi. 10.1038/jhg.2014.87
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- Article
An A/C germline single-nucleotide polymorphism in the TNFAIP3 gene is associated with advanced disease stage and survival in only surgically treated esophageal cancer.
- Published in:
- Journal of Human Genetics, 2014, v. 59, n. 12, p. 661, doi. 10.1038/jhg.2014.90
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- Article
Recurrence risks for different pregnancy outcomes and meiotic segregation analysis of spermatozoa in carriers of t(1;11)(p36.22;q12.2).
- Published in:
- Journal of Human Genetics, 2014, v. 59, n. 12, p. 667, doi. 10.1038/jhg.2014.92
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- Article