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Journal of Human Genetics|November 28, 2001
Homozygosity and linkage disequilibrium mapping of autosomal recessive distal myopathy (Nonaka distal myopathy)T Asaka, K Ikeuchi, S Okino, et al.Journal of Human Genetics|November 28, 2001
Identification of human multidrug resistance protein 1 (MRP1) mutations and characterization of a G671V substitutionS Conrad, H M Kauffmann, K Ito, et al.Journal of Human Genetics|November 28, 2001
Mutation and association analysis of the interferon regulatory factor 2 gene (IRF2) with atopic dermatitisY Nishio, E Noguchi, S Ito, et al.Journal of Human Genetics|February 24, 2001
Association of estrogen receptor beta (ESR2) gene polymorphism with blood pressureS Ogawa, M Emi, M Shiraki, et al.Journal of Human Genetics|February 24, 2001
Novel polymorphisms of prostate-specific antigen (PSA) gene associated with PSA mRNA expression in breast cancerQ F Yang, T Sakurai, L Shan, et al.Journal of Human Genetics|June 18, 2003
STR polymorphisms of "forensic loci" in the northern Han Chinese populationWei Wang, Huiling Jia, Qin Wang, et al.Journal of Human Genetics|July 29, 2003
Identification of a novel 2026G-->C mutation of the MRP2 gene in a Japanese patient with Dubin-Johnson syndromeShinya Wakusawa, Ikuo Machida, Satoshi Suzuki, et al.Journal of Human Genetics|August 9, 2003
Extreme androgen resistance in a kindred with a novel insertion/deletion mutation in exon 5 of the androgen receptor geneFelipe Vilchis, Luis Ramos, Susana Kofman-Alfaro, et al.Journal of Human Genetics|August 26, 2003
Anion exchanger 1 mutations associated with distal renal tubular acidosis in the Thai populationPa-Thai Yenchitsomanus, Nunghathai Sawasdee, Atchara Paemanee, et al.Journal of Human Genetics|August 28, 2003
Homozygous mutation Arg768Trp in the ABC-transporter encoding gene MRP2/cMOAT/ABCC2 causes Dubin-Johnson syndrome in a Caucasian patientVerena Materna, Hermann LagePageof 352