Works matching IS 03406717 AND DT 2003 AND VI 113 AND IP 3
Results: 14
The origins and genetic structure of three co-resident Chinese Muslim populations: the Salar, Bo'an and Dongxiang.
- Published in:
- Human Genetics, 2003, v. 113, n. 3, p. 244, doi. 10.1007/s00439-003-0948-y
- By:
- Publication type:
- Article
Analysis of zinc transporter, hZnT4 (Slc30A4), gene expression in a mammary gland disorder leading to reduced zinc secretion into milk.
- Published in:
- Human Genetics, 2003, v. 113, n. 3, p. 202, doi. 10.1007/s00439-003-0952-2
- By:
- Publication type:
- Article
Sequence variation in the CHAT locus shows no association with late-onset Alzheimer's disease.
- Published in:
- Human Genetics, 2003, v. 113, n. 3, p. 258, doi. 10.1007/s00439-003-0960-2
- By:
- Publication type:
- Article
Markers informative for ancestry demonstrate consistent megabase-length linkage disequilibrium in the African American population.
- Published in:
- Human Genetics, 2003, v. 113, n. 3, p. 211, doi. 10.1007/s00439-003-0961-1
- By:
- Publication type:
- Article
Impact of public health strategies on the birth prevalence of cystic fibrosis in Brittany, France.
- Published in:
- Human Genetics, 2003, v. 113, n. 3, p. 280, doi. 10.1007/s00439-003-0962-0
- By:
- Publication type:
- Article
Increased prevalence of CFTR mutations and variants and decreased chloride secretion in primary sclerosing cholangitis.
- Published in:
- Human Genetics, 2003, v. 113, n. 3, p. 286, doi. 10.1007/s00439-003-0963-z
- By:
- Publication type:
- Article
The association between Japanese primary open-angle glaucoma and normal tension glaucoma patients and the optineurin gene.
- Published in:
- Human Genetics, 2003, v. 113, n. 3, p. 276, doi. 10.1007/s00439-003-0964-y
- By:
- Publication type:
- Article
Comparison of strategies for selecting single nucleotide polymorphisms for case/control association studies.
- Published in:
- Human Genetics, 2003, v. 113, n. 3, p. 253, doi. 10.1007/s00439-003-0965-x
- By:
- Publication type:
- Article
Increased variation in mtDNA in patients with familial sensorineural hearing impairment.
- Published in:
- Human Genetics, 2003, v. 113, n. 3, p. 220, doi. 10.1007/s00439-003-0966-9
- By:
- Publication type:
- Article
Genome-wide homozygosity mapping localizes a gene for autosomal recessive non-progressive infantile ataxia to 20q11-q13.
- Published in:
- Human Genetics, 2003, v. 113, n. 3, p. 293, doi. 10.1007/s00439-003-0967-8
- By:
- Publication type:
- Article
Lung cancer risk in germline p53 mutation carriers: association between an inherited cancer predisposition, cigarette smoking, and cancer risk.
- Published in:
- Human Genetics, 2003, v. 113, n. 3, p. 238, doi. 10.1007/s00439-003-0968-7
- By:
- Publication type:
- Article
Altitude is a phenotypic modifier in hereditary paraganglioma type 1: evidence for an oxygen-sensing defect.
- Published in:
- Human Genetics, 2003, v. 113, n. 3, p. 228, doi. 10.1007/s00439-003-0969-6
- By:
- Publication type:
- Article
Novel types of mutation in the choroideremia (CHM) gene: a full-length L1 insertion and an intronic mutation activating a cryptic exon.
- Published in:
- Human Genetics, 2003, v. 113, n. 3, p. 268, doi. 10.1007/s00439-003-0970-0
- By:
- Publication type:
- Article
Mutational analysis of the human FATE gene in 144 infertile men.
- Published in:
- Human Genetics, 2003, v. 113, n. 3, p. 195, doi. 10.1007/s00439-003-0974-9
- By:
- Publication type:
- Article