Works matching IS 10614036 AND DT 1998 AND VI 20 AND IP 3
Results: 28
SNP attack on complex traits.
- Published in:
- Nature Genetics, 1998, v. 20, n. 3, p. 217, doi. 10.1038/3011
- Publication type:
- Article
Women on the move.
- Published in:
- Nature Genetics, 1998, v. 20, n. 3, p. 219, doi. 10.1038/3012
- By:
- Publication type:
- Article
Life, death and nuclear spots.
- Published in:
- Nature Genetics, 1998, v. 20, n. 3, p. 220, doi. 10.1038/3014
- By:
- Publication type:
- Article
The zebrafish and haematopoietic justice.
- Published in:
- Nature Genetics, 1998, v. 20, n. 3, p. 222, doi. 10.1038/3016
- By:
- Publication type:
- Article
Type 2 diabetes ? who is conducting the orchestra?
- Published in:
- Nature Genetics, 1998, v. 20, n. 3, p. 223, doi. 10.1038/3018
- By:
- Publication type:
- Article
Touching Base.
- Published in:
- Nature Genetics, 1998, v. 20, n. 3, p. 226, doi. 10.1038/3021
- Publication type:
- Article
Stable dicentric X chromosomes with two functional centromeres.
- Published in:
- Nature Genetics, 1998, v. 20, n. 3, p. 227, doi. 10.1038/3024
- By:
- Publication type:
- Article
Fetal exposure to DES results in de-regulation of Wnt7a during uterine morphogenesis.
- Published in:
- Nature Genetics, 1998, v. 20, n. 3, p. 228, doi. 10.1038/3027
- By:
- Publication type:
- Article
Differential SMN2 expression associated with SMA severity.
- Published in:
- Nature Genetics, 1998, v. 20, n. 3, p. 230, doi. 10.1038/3030
- By:
- Publication type:
- Article
DRPLA aggregation and transglutaminase, revisited.
- Published in:
- Nature Genetics, 1998, v. 20, n. 3, p. 231, doi. 10.1038/3033
- By:
- Publication type:
- Article
A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasis.
- Published in:
- Nature Genetics, 1998, v. 20, n. 3, p. 233, doi. 10.1038/3034
- By:
- Publication type:
- Article
A zebrafish model for hepatoerythropoietic porphyria.
- Published in:
- Nature Genetics, 1998, v. 20, n. 3, p. 239, doi. 10.1038/3041
- By:
- Publication type:
- Article
Positional cloning of the zebrafish sauternes gene: a model for congenital sideroblastic anaemia.
- Published in:
- Nature Genetics, 1998, v. 20, n. 3, p. 244, doi. 10.1038/3049
- By:
- Publication type:
- Article
Progressive ataxia, myoclonic epilepsy and cerebellar apoptosis in cystatin B-deficient mice.
- Published in:
- Nature Genetics, 1998, v. 20, n. 3, p. 251, doi. 10.1038/3059
- By:
- Publication type:
- Article
PML induces a novel caspase-independent death process.
- Published in:
- Nature Genetics, 1998, v. 20, n. 3, p. 259, doi. 10.1038/3068
- By:
- Publication type:
- Article
Pml is essential for multiple apoptotic pathways.
- Published in:
- Nature Genetics, 1998, v. 20, n. 3, p. 266, doi. 10.1038/3073
- By:
- Publication type:
- Article
A gene encoding a novel RFX-associated transactivator is mutated in the majority of MHC class II deficiency patients.
- Published in:
- Nature Genetics, 1998, v. 20, n. 3, p. 273, doi. 10.1038/3081
- By:
- Publication type:
- Article
Genetic evidence for a higher female migration rate in humans.
- Published in:
- Nature Genetics, 1998, v. 20, n. 3, p. 278, doi. 10.1038/3088
- By:
- Publication type:
- Article
The Fanconi anaemia group G gene FANCG is identical with XRCC9.
- Published in:
- Nature Genetics, 1998, v. 20, n. 3, p. 281, doi. 10.1038/3093
- By:
- Publication type:
- Article
A Pro12Ala substitution in PPARγ2 associated with decreased receptor activity, lower body mass index and improved insulin sensitivity.
- Published in:
- Nature Genetics, 1998, v. 20, n. 3, p. 284, doi. 10.1038/3099
- By:
- Publication type:
- Article
Rapid amplification of a retrotransposon subfamily is evolving the mouse genome.
- Published in:
- Nature Genetics, 1998, v. 20, n. 3, p. 288, doi. 10.1038/3104
- By:
- Publication type:
- Article
Somatic mutations of the mitochondrial genome in human colorectal tumours.
- Published in:
- Nature Genetics, 1998, v. 20, n. 3, p. 291, doi. 10.1038/3108
- By:
- Publication type:
- Article
Impaired glucose tolerance in mice with a targeted impairment of insulin action in muscle and adipose tissue.
- Published in:
- Nature Genetics, 1998, v. 20, n. 3, p. 294, doi. 10.1038/3112
- By:
- Publication type:
- Article
Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction.
- Published in:
- Nature Genetics, 1998, v. 20, n. 3, p. 299, doi. 10.1038/3118
- By:
- Publication type:
- Article
A genome-wide scan for human obesity genes reveals a major susceptibility locus on chromosome 10.
- Published in:
- Nature Genetics, 1998, v. 20, n. 3, p. 304, doi. 10.1038/3123
- By:
- Publication type:
- Article
Esx1 is an X-chromosome-imprinted regulator of placental development and fetal growth.
- Published in:
- Nature Genetics, 1998, v. 20, n. 3, p. 309, doi. 10.1038/3129
- By:
- Publication type:
- Article
Assignment of Tangier disease to chromosome 9q31 by a graphical linkage exclusion strategy.
- Published in:
- 1998
- By:
- Publication type:
- Erratum
Inversin, a novel gene in the vertebrate left-right axis pathway, is partially deleted in the inv mouse.
- Published in:
- 1998
- By:
- Publication type:
- Erratum