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Journal of Human Genetics|April 20, 2001
Glycogen storage disease type Ia: molecular study in Brazilian patientsF de C Reis, H C Caldas, D Y Norato, et al.Journal of Human Genetics|April 20, 2001
Identification and allelic frequencies of novel single-nucleotide polymorphisms in the DUSP1 and BTG1 genesC Suzuki, M Unoki, Y NakamuraJournal of Human Genetics|April 20, 2001
Multiple single-nucleotide polymorphisms (SNPs) in the Japanese population in six candidate genes for long QT syndromeH Iwasa, M Kurabayashi, R Nagai, et al.Journal of Human Genetics|April 27, 2001
The c-Jun NH2-terminal kinase3 (JNK3) gene: genomic structure, chromosomal assignment, and loss of expression in brain tumorsS Yoshida, K Fukino, H Harada, et al.Journal of Human Genetics|April 27, 2001
Establishment of an optimized set of 406 microsatellite markers covering the whole genome for the Japanese populationK Ikari, H Onda, K Furushima, et al.Journal of Human Genetics|September 18, 2001
The hemoglobin O mutation in Indonesia: distribution and phenotypic expressionD Daud, A Harahap, I Setianingsih, et al.Journal of Human Genetics|September 18, 2001
Mutations of the PKD1 gene among Japanese autosomal dominant polycystic kidney disease patients, including one heterozygous mutation identified in members of the same familyM Mizoguchi, T Tamura, A Yamaki, et al.Journal of Human Genetics|September 18, 2001
Genetic features of hearing loss associated with ear anomalies: PDS and EYA1 mutation analysisA Namba, S Abe, H Shinkawa, et al.Journal of Human Genetics|November 28, 2001
Molecular and cell biological aspects of Alzheimer diseaseB S ShastryJournal of Human Genetics|May 17, 2003
Association of positional and functional candidate genes FGF1, FBN2, and LOX on 5q31 with intracranial aneurysmTaku Yoneyama, Hidetoshi Kasuya, Hideaki Onda, et al.Pageof 351