Works matching IS 10614036 AND DT 1999 AND VI 21 AND IP 4
Results: 29
Publishing paradigms.
- Published in:
- 1999
- Publication type:
- Editorial
Anti-Xistentialism.
- Published in:
- Nature Genetics, 1999, v. 21, n. 4, p. 343, doi. 10.1038/7661
- By:
- Publication type:
- Article
Mediating immunity to mycobacteria.
- Published in:
- Nature Genetics, 1999, v. 21, n. 4, p. 345, doi. 10.1038/7663
- By:
- Publication type:
- Article
A vital role for vitamin A.
- Published in:
- Nature Genetics, 1999, v. 21, n. 4, p. 346, doi. 10.1038/7665
- By:
- Publication type:
- Article
Making sense out of sound.
- Published in:
- Nature Genetics, 1999, v. 21, n. 4, p. 347, doi. 10.1038/7668
- By:
- Publication type:
- Article
Touchingbase.
- Published in:
- Nature Genetics, 1999, v. 21, n. 4, p. 351
- Publication type:
- Article
A common nonsense mutation results in α-actinin-3 deficiency in the general population.
- Published in:
- Nature Genetics, 1999, v. 21, n. 4, p. 353, doi. 10.1038/7675
- By:
- Publication type:
- Article
A mutation in NRL is associated with autosomal dominant retinitis pigmentosa.
- Published in:
- Nature Genetics, 1999, v. 21, n. 4, p. 355, doi. 10.1038/7678
- By:
- Publication type:
- Article
Counting the repetitive kringle-IV repeats in the gene encoding human apolipoprotein(a) by fibre-FISH.
- Published in:
- Nature Genetics, 1999, v. 21, n. 4, p. 357, doi. 10.1038/7681
- By:
- Publication type:
- Article
Atm haploinsufficiency results in increased sensitivity to sublethal doses of ionizing radiation in mice.
- Published in:
- Nature Genetics, 1999, v. 21, n. 4, p. 359, doi. 10.1038/7684
- By:
- Publication type:
- Article
Loss of information due to ambiguous haplotyping of SNPs.
- Published in:
- Nature Genetics, 1999, v. 21, n. 4, p. 360, doi. 10.1038/7687
- By:
- Publication type:
- Article
Genetic determinism and the overprotection of human subjects.
- Published in:
- Nature Genetics, 1999, v. 21, n. 4, p. 362, doi. 10.1038/7692
- By:
- Publication type:
- Article
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
- Published in:
- Nature Genetics, 1999, v. 21, n. 4, p. 363, doi. 10.1038/7693
- By:
- Publication type:
- Article
A human IFNGR1 small deletion hotspot associated with dominant susceptibility to mycobacterial infection.
- Published in:
- Nature Genetics, 1999, v. 21, n. 4, p. 370, doi. 10.1038/7701
- By:
- Publication type:
- Article
An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8).
- Published in:
- Nature Genetics, 1999, v. 21, n. 4, p. 379, doi. 10.1038/7710
- By:
- Publication type:
- Article
Comparative genomes of Chlamydia pneumoniae and C. trachomatis.
- Published in:
- Nature Genetics, 1999, v. 21, n. 4, p. 385, doi. 10.1038/7716
- By:
- Publication type:
- Article
Independent regulation of the two Pax5 alleles during B-cell development.
- Published in:
- Nature Genetics, 1999, v. 21, n. 4, p. 390, doi. 10.1038/7720
- By:
- Publication type:
- Article
Transferrin receptor is necessary for development of erythrocytes and the nervous system.
- Published in:
- Nature Genetics, 1999, v. 21, n. 4, p. 396, doi. 10.1038/7727
- By:
- Publication type:
- Article
Tsix, a gene antisense to Xist at the X-inactivation centre.
- Published in:
- Nature Genetics, 1999, v. 21, n. 4, p. 400, doi. 10.1038/7734
- By:
- Publication type:
- Article
Interacting loci cause severe iris atrophy and glaucoma in DBA/2J mice.
- Published in:
- Nature Genetics, 1999, v. 21, n. 4, p. 405, doi. 10.1038/7741
- By:
- Publication type:
- Article
A common human skin tumour is caused by activating mutations in β-catenin.
- Published in:
- Nature Genetics, 1999, v. 21, n. 4, p. 410, doi. 10.1038/7747
- By:
- Publication type:
- Article
The complete family of genes encoding G proteins of Caenorhabditis elegans.
- Published in:
- Nature Genetics, 1999, v. 21, n. 4, p. 414, doi. 10.1038/7753
- By:
- Publication type:
- Article
Identification of the gene responsible for gelatinous drop-like corneal dystrophy.
- Published in:
- Nature Genetics, 1999, v. 21, n. 4, p. 420, doi. 10.1038/7759
- By:
- Publication type:
- Article
A novel endothelial-derived lipase that modulates HDL metabolism.
- Published in:
- Nature Genetics, 1999, v. 21, n. 4, p. 424, doi. 10.1038/7766
- By:
- Publication type:
- Article
Retroposition of autosomal mRNA yielded testis-specific gene family on human Y chromosome.
- Published in:
- Nature Genetics, 1999, v. 21, n. 4, p. 429, doi. 10.1038/7771
- By:
- Publication type:
- Article
The gene encoding proline dehydrogenase modulates sensorimotor gating in mice.
- Published in:
- Nature Genetics, 1999, v. 21, n. 4, p. 434, doi. 10.1038/7777
- By:
- Publication type:
- Article
The Pendred syndrome gene encodes a chloride-iodide transport protein.
- Published in:
- Nature Genetics, 1999, v. 21, n. 4, p. 440, doi. 10.1038/7783
- By:
- Publication type:
- Article
Embryonic retinoic acid synthesis is essential for early mouse post-implantation development.
- Published in:
- Nature Genetics, 1999, v. 21, n. 4, p. 444, doi. 10.1038/7788
- By:
- Publication type:
- Article
Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment.
- Published in:
- 1999
- By:
- Publication type:
- Erratum