Works matching IS 10614036 AND DT 1999 AND VI 23 AND IP 2
Results: 32
Annote bene.
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- Nature Genetics, 1999, v. 23, n. 2, p. 125, doi. 10.1038/13750
- Publication type:
- Article
Breaking the silence in Rett syndrome.
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- Nature Genetics, 1999, v. 23, n. 2, p. 127, doi. 10.1038/13751
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A friendly signal.
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- Nature Genetics, 1999, v. 23, n. 2, p. 128, doi. 10.1038/13753
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- Article
The Kudos of non-homologous end-joining.
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- Nature Genetics, 1999, v. 23, n. 2, p. 130, doi. 10.1038/13755
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- Article
Flower power.
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- Nature Genetics, 1999, v. 23, n. 2, p. 132, doi. 10.1038/13757
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- Article
Incriminating gene suspects, Prader-Willi style.
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- Nature Genetics, 1999, v. 23, n. 2, p. 132, doi. 10.1038/13758
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- Article
A new angle on a pervasive oncogene.
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- Nature Genetics, 1999, v. 23, n. 2, p. 134, doi. 10.1038/13761
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- Article
TOUCHINGbase.
- Published in:
- Nature Genetics, 1999, v. 23, n. 2, p. 137
- Publication type:
- Article
Absence of genome-wide changes in DNA methylation during development of the zebrafish.
- Published in:
- Nature Genetics, 1999, v. 23, n. 2, p. 139, doi. 10.1038/13767
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- Article
Dysferlin deletion in SJL mice (SJL-Dysf) defines a natural model for limb girdle muscular dystrophy 2B.
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- Nature Genetics, 1999, v. 23, n. 2, p. 141, doi. 10.1038/13770
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- Article
Familial endometrial cancer in female carriers of MSH6 germline mutations.
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- Nature Genetics, 1999, v. 23, n. 2, p. 142, doi. 10.1038/13773
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- Article
The fusion gene Cbfb-MYH11 blocks myeloid differentiation and predisposes mice to acute myelomonocytic leukaemia.
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- Nature Genetics, 1999, v. 23, n. 2, p. 144, doi. 10.1038/13776
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- Article
Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA.
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- Nature Genetics, 1999, v. 23, n. 2, p. 147, doi. 10.1038/13779
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- Article
Why and how we age.
- Published in:
- 1999
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- Book Review
Structural genomics: beyond the Human Genome Project.
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- Nature Genetics, 1999, v. 23, n. 2, p. 151, doi. 10.1038/13783
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- Article
Fv2 encodes a truncated form of the Stk receptor tyrosine kinase.
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- Nature Genetics, 1999, v. 23, n. 2, p. 159, doi. 10.1038/13787
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- Publication type:
- Article
Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia.
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- Nature Genetics, 1999, v. 23, n. 2, p. 166, doi. 10.1038/13793
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- Article
Genomic instability in Gadd45a-deficient mice.
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- Nature Genetics, 1999, v. 23, n. 2, p. 176, doi. 10.1038/13802
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- Article
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2.
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- Nature Genetics, 1999, v. 23, n. 2, p. 185, doi. 10.1038/13810
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- Article
Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomas.
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- Nature Genetics, 1999, v. 23, n. 2, p. 189, doi. 10.1038/13815
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- Article
Mre11 and Ku70 interact in somatic cells, but are differentially expressed in early meiosis.
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- Nature Genetics, 1999, v. 23, n. 2, p. 194, doi. 10.1038/13821
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- Article
Disruption of the mouse necdin gene results in early post-natal lethality.
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- Nature Genetics, 1999, v. 23, n. 2, p. 199
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- Article
Genome-wide mapping with biallelic markers in Arabidopsis thaliana.
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- Nature Genetics, 1999, v. 23, n. 2, p. 203, doi. 10.1038/13833
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- Article
Mutations in the skeletal muscle α-actin gene in patients with actin myopathy and nemaline myopathy.
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- Nature Genetics, 1999, v. 23, n. 2, p. 208, doi. 10.1038/13837
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- Article
Early specification of limb muscle precursor cells by the homeobox gene Lbx1h.
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- Nature Genetics, 1999, v. 23, n. 2, p. 213
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- Article
Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12).
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- Nature Genetics, 1999, v. 23, n. 2, p. 217, doi. 10.1038/13848
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- Article
Repression of the gene encoding the TGF-β type II receptor is a major target of the EWS-FLI1 oncoprotein.
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- Nature Genetics, 1999, v. 23, n. 2, p. 222, doi. 10.1038/13854
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- Publication type:
- Article
Mice lacking the folic acid-binding protein Folbp1 are defective in early embryonic development.
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- Nature Genetics, 1999, v. 23, n. 2, p. 228, doi. 10.1038/13861
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- Article
The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations in CLN8.
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- Nature Genetics, 1999, v. 23, n. 2, p. 233, doi. 10.1038/13868
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- Article
Susceptibility to testicular germ-cell tumours in a 129.MOLF-Chr 19 chromosome substitution strain.
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- Nature Genetics, 1999, v. 23, n. 2, p. 237, doi. 10.1038/13874
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- Article
Functional screening of an asthma QTL in YAC transgenic mice.
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- Nature Genetics, 1999, v. 23, n. 2, p. 241, doi. 10.1038/13880
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- Article
Loss of Cul1 results in early embryonic lethality and dysregulation of cyclin E.
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- Nature Genetics, 1999, v. 23, n. 2, p. 245, doi. 10.1038/13886
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- Article