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- Published in:
- 1998
- Publication type:
- Editorial
Sometimes it's hot, sometimes it's not.
- Published in:
- Nature Genetics, 1998, v. 19, n. 3, p. 213, doi. 10.1038/881
- By:
- Publication type:
- Article
A recombination hotspot responsible for two inherited peripheral neuropathies is located near a mariner transposon-like element.
- Published in:
- 1998
- By:
- Publication type:
- Erratum
Weighing in on diabetes risk.
- Published in:
- Nature Genetics, 1998, v. 19, n. 3, p. 209, doi. 10.1038/876
- By:
- Publication type:
- Article
Vertebrate genome evolution and the zebrafish gene map.
- Published in:
- 1998
- By:
- Publication type:
- Erratum
Counting on Xist.
- Published in:
- Nature Genetics, 1998, v. 19, n. 3, p. 211, doi. 10.1038/878
- By:
- Publication type:
- Article
Non-invasive sexing of preimplantation stage mammalian embryos.
- Published in:
- Nature Genetics, 1998, v. 19, n. 3, p. 220, doi. 10.1038/893
- By:
- Publication type:
- Article
Nuclear power and mitochondrial disease.
- Published in:
- Nature Genetics, 1998, v. 19, n. 3, p. 214, doi. 10.1038/883
- By:
- Publication type:
- Article
Touching Base.
- Published in:
- Nature Genetics, 1998, v. 19, n. 3, p. 218, doi. 10.1038/888
- Publication type:
- Article
It's raining SNPs, hallelujah?
- Published in:
- Nature Genetics, 1998, v. 19, n. 3, p. 216, doi. 10.1038/885
- By:
- Publication type:
- Article
Cloning and characterization of a family of novel mammalian DNA (cytosine-5) methyltransferases.
- Published in:
- Nature Genetics, 1998, v. 19, n. 3, p. 219, doi. 10.1038/890
- By:
- Publication type:
- Article
Human genome annotation ? a possible role for HUGO?
- Published in:
- Nature Genetics, 1998, v. 19, n. 3, p. 222, doi. 10.1038/896
- By:
- Publication type:
- Article
PTEN and inherited hamartoma-cancer syndromes.
- Published in:
- Nature Genetics, 1998, v. 19, n. 3, p. 223, doi. 10.1038/897
- By:
- Publication type:
- Article
Mutation detection and single-molecule counting using isothermal rolling-circle amplification.
- Published in:
- Nature Genetics, 1998, v. 19, n. 3, p. 225, doi. 10.1038/898
- By:
- Publication type:
- Article
DNA sequence diversity in a 9.7-kb region of the human lipoprotein lipase gene.
- Published in:
- Nature Genetics, 1998, v. 19, n. 3, p. 233, doi. 10.1038/907
- By:
- Publication type:
- Article
Identification of the gene responsible for Best macular dystrophy.
- Published in:
- Nature Genetics, 1998, v. 19, n. 3, p. 241, doi. 10.1038/915
- By:
- Publication type:
- Article
Role of the region 3′ to Xist exon 6 in the counting process of X-chromosome inactivation.
- Published in:
- Nature Genetics, 1998, v. 19, n. 3, p. 249, doi. 10.1038/924
- By:
- Publication type:
- Article
BRCA1 protein is linked to the RNA polymerase II holoenzyme complex via RNA helicase A.
- Published in:
- Nature Genetics, 1998, v. 19, n. 3, p. 254, doi. 10.1038/930
- By:
- Publication type:
- Article
Total colourblindness is caused by mutations in the gene encoding the α-subunit of the cone photoreceptor cGMP-gated cation channel.
- Published in:
- Nature Genetics, 1998, v. 19, n. 3, p. 257, doi. 10.1038/935
- By:
- Publication type:
- Article
An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness.
- Published in:
- Nature Genetics, 1998, v. 19, n. 3, p. 260, doi. 10.1038/940
- By:
- Publication type:
- Article
Loss-of-function mutations in a calcium-channel α<sub>1</sub>-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness.
- Published in:
- Nature Genetics, 1998, v. 19, n. 3, p. 264, doi. 10.1038/947
- By:
- Publication type:
- Article
Mutations in the glucokinase gene of the fetus result in reduced birth weight.
- Published in:
- Nature Genetics, 1998, v. 19, n. 3, p. 268, doi. 10.1038/953
- By:
- Publication type:
- Article
Mutation in Npps in a mouse model of ossification of the posterior longitudinal ligament of the spine.
- Published in:
- Nature Genetics, 1998, v. 19, n. 3, p. 271, doi. 10.1038/956
- By:
- Publication type:
- Article
The mouse pudgy mutation disrupts Delta homologue Dll3 and initiation of early somite boundaries.
- Published in:
- Nature Genetics, 1998, v. 19, n. 3, p. 274, doi. 10.1038/961
- By:
- Publication type:
- Article
Mutations in the mineralocorticoid receptor gene cause autosomal dominant pseudohypoaldosteronism type I.
- Published in:
- Nature Genetics, 1998, v. 19, n. 3, p. 279, doi. 10.1038/966
- By:
- Publication type:
- Article
Renal and intestinal absorptive defects in mice lacking the NHE3 Na<sup>+</sup>/H<sup>+</sup> exchanger.
- Published in:
- Nature Genetics, 1998, v. 19, n. 3, p. 282, doi. 10.1038/969
- By:
- Publication type:
- Article
CLN5, a novel gene encoding a putative transmembrane protein mutated in Finnish variant late infantile neuronal ceroid lipofuscinosis.
- Published in:
- Nature Genetics, 1998, v. 19, n. 3, p. 286, doi. 10.1038/975
- By:
- Publication type:
- Article
Loss of adenylyl cyclase I activity disrupts patterning of mouse somatosensory cortex.
- Published in:
- Nature Genetics, 1998, v. 19, n. 3, p. 289, doi. 10.1038/980
- By:
- Publication type:
- Article
A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitus.
- Published in:
- Nature Genetics, 1998, v. 19, n. 3, p. 292, doi. 10.1038/985
- By:
- Publication type:
- Article
A search for type 1 diabetes susceptibility genes in families from the United Kingdom.
- Published in:
- Nature Genetics, 1998, v. 19, n. 3, p. 297, doi. 10.1038/991
- By:
- Publication type:
- Article
A male-female bias in type 1 diabetes and linkage to chromosome Xp in MHC HLA-DR3-positive patients.
- Published in:
- Nature Genetics, 1998, v. 19, n. 3, p. 301, doi. 10.1038/995
- By:
- Publication type:
- Article
Mutations in GDI1 are responsible for X-linked non-specific mental retardation.
- Published in:
- 1998
- By:
- Publication type:
- Erratum