Infrequent genetic alterations of the PTEN gene in Japanese patients with sporadic prostate cancer.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 4, p. 228, doi. 10.1007/s100380050078
- By:
- Publication type:
- Article
Works matching IS 14345161 AND DT 1998 AND VI 43 AND IP 4
Results: 20
1
2
Mutation analysis of the phenylalanine hydroxylase gene and its clinical implications in two Japanese patients with non-phenylketonuria hyperphenylalaninemia.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 4, p. 231, doi. 10.1007/s100380050079
- By:
- Publication type:
- Article
3
Anticipation in Japanese families with schizophrenia.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 4, p. 217, doi. 10.1007/s100380050076
- By:
- Publication type:
- Article
4
New dominant syndrome of microcephaly, facial abnormalities, micromelia, and mental retardation.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 4, p. 224, doi. 10.1007/s100380050077
- By:
- Publication type:
- Article
5
Molecular diagnosis of patients with β-thalassemia major in central Taiwan by amplified created restriction site analysis.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 4, p. 237, doi. 10.1007/s100380050080
- By:
- Publication type:
- Article
6
Mitochondrial DNA mutations in Japanese patients with optic neuropathy unassociated with a mutation at nucleotide position 11,778.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 4, p. 242, doi. 10.1007/s100380050081
- By:
- Publication type:
- Article
7
Further evidence for a major ancient mutation underlying myotonic dystrophy from linkage disequilibrium studies in the Japanese population.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 4, p. 246, doi. 10.1007/s100380050082
- By:
- Publication type:
- Article
8
Five familial hypercholesterolemic kindreds in Japan with novel mutations of the LDL receptor gene.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 4, p. 250, doi. 10.1007/s100380050083
- By:
- Publication type:
- Article
9
Isolation and mapping of a novel human kidney- and liver-specific gene homologous to the bacterial acetyltransferases.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 4, p. 255, doi. 10.1007/s100380050084
- By:
- Publication type:
- Article
10
Novel missense mutation resulting in the substitution of tyrosine by cysteine at codon 597 of the type X collagen gene associated with Schmid metaphyseal chondrodysplasia.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 4, p. 259, doi. 10.1007/s100380050085
- By:
- Publication type:
- Article
11
Cloning and characterization of the murine P2XM receptor gene.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 4, p. 262, doi. 10.1007/s100380050086
- By:
- Publication type:
- Article
12
Cloning, expression analysis, and chromosomal localization of HIP1R, an isolog of huntingtin interacting protein (HIP1).
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 4, p. 268, doi. 10.1007/s100380050087
- By:
- Publication type:
- Article
13
Isolation, tissue expression, and chromosomal assignment of a novel human gene which encodes a protein with RING finger motif.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 4, p. 272, doi. 10.1007/s100380050088
- By:
- Publication type:
- Article
14
Chromosomal assignment of the gene for human DNA-PKcs interacting protein (KIP) on chromosome 15q25.3-q26.1 by somatic hybrid analysis and fluorescence in situ hybridization.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 4, p. 275, doi. 10.1007/s100380050089
- By:
- Publication type:
- Article
15
A highly polymorphic CA repeat marker at the human tumor necrosis factor alpha (TNFAα) locus.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 4, p. 278, doi. 10.1007/s100380050090
- By:
- Publication type:
- Article
16
Isolation and radiation hybrid mapping of a dinucleotide repeat polymorphism at the human calcium-sensing receptor (CASR) locus.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 4, p. 280, doi. 10.1007/s100380050091
- By:
- Publication type:
- Article
17
A HhaI/BstUI polymorphism in a novel gene at human chromosome 11p15.5.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 4, p. 283, doi. 10.1007/s100380050092
- By:
- Publication type:
- Article
18
A GT dinucleotide repeat polymorphism in intron 1 of the H-cadherin (CDH13) gene.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 4, p. 285, doi. 10.1007/s100380050093
- By:
- Publication type:
- Article
19
Isolation of a polymorphic CA repeat sequence at the human progesterone receptor (PGR) locus.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 4, p. 287, doi. 10.1007/s100380050094
- By:
- Publication type:
- Article
20
A highly polymorphic CA repeat marker at the human interleukin 6 receptor (IL6R) locus.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 4, p. 289, doi. 10.1007/s100380050095
- By:
- Publication type:
- Article