Works matching IS 14345161 AND DT 1998 AND VI 43 AND IP 3
Results: 17
VNTR (variable number of tandem repeat) sequences as transcriptional, translational, or functional regulators.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 3, p. 149, doi. 10.1007/s100380050059
- By:
- Publication type:
- Article
Association and linkage of LDLR gene variation with variation in plasma low density lipoprotein cholesterol.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 3, p. 153, doi. 10.1007/s100380050060
- By:
- Publication type:
- Article
A novel missense mutation of the tissue-nonspecific alkaline phosphatase gene detected in a patient with hypophosphatasia.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 3, p. 160, doi. 10.1007/s100380050061
- By:
- Publication type:
- Article
Heterozygosities and allelic frequencies of 358 dinucleotide-repeat marker loci in the Japanese population.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 3, p. 165, doi. 10.1007/s100380050062
- By:
- Publication type:
- Article
Expression and chromosomal localization of KIAA0369, a putative kinase structurally related to Doublecortin.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 3, p. 169, doi. 10.1007/s100380050063
- By:
- Publication type:
- Article
Interstitial deletion of chromosome 7q in a patient with Williams syndrome and infantile spasms.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 3, p. 178, doi. 10.1007/s100380050064
- By:
- Publication type:
- Article
A novel mutation of coproporphyrinogen oxidase (CPO) gene in a Japanese family.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 3, p. 182, doi. 10.1007/s100380050065
- By:
- Publication type:
- Article
Molecular phylogenetics of the hominoid Y chromosome.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 3, p. 185, doi. 10.1007/s100380050066
- By:
- Publication type:
- Article
Identification of amplified DNA sequences on double minute chromosomes in a leukemic cell line KY821 by means of spectral karyotyping and comparative genomic hybridization.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 3, p. 187, doi. 10.1007/s100380050067
- By:
- Publication type:
- Article
Joint laxity, vitreoretinal degeneration, facial abnormalities, and generalized skeletal alterations: A new syndrome?
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 3, p. 191, doi. 10.1007/s100380050068
- By:
- Publication type:
- Article
Y-Specific DNA polymorphisms of the YAP element and the locus DYS19 in the Korean population.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 3, p. 195, doi. 10.1007/s100380050069
- By:
- Publication type:
- Article
Novel MEN1 gene mutations in familial multiple endocrine neoplasia type 1.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 3, p. 199, doi. 10.1007/s100380050070
- By:
- Publication type:
- Article
Isolation, tissue expression, and chromosomal assignment of human RGS5, a novel G-protein signaling regulator gene.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 3, p. 202, doi. 10.1007/s100380050071
- By:
- Publication type:
- Article
Connatal Pelizaeus-Merzbacher disease: A missense mutation in exon 4 of the proteolipid protein (PLP) gene.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 3, p. 206, doi. 10.1007/s100380050072
- By:
- Publication type:
- Article
Assignment of the ZIP kinase gene to human chromosome 19p13.3 by somatic hybrid analysis and fluorescence in-situ hybridization.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 3, p. 209, doi. 10.1007/s100380050073
- By:
- Publication type:
- Article
Dinucleotide repeat polymorphism in the first intron of the CSR gene.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 3, p. 212, doi. 10.1007/s100380050074
- By:
- Publication type:
- Article
Novel polymorphisms in the βig-h3 gene.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 3, p. 214, doi. 10.1007/s100380050075
- By:
- Publication type:
- Article