Works matching IS 14345161 AND DT 2001 AND VI 46 AND IP 12
Results: 10
Characterization of a familial RCC-associated t(2;3)(q33;q21) chromosome translocation.
- Published in:
- Journal of Human Genetics, 2001, v. 46, n. 12, p. 685, doi. 10.1007/s100380170001
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- Article
Genetic polymorphisms in the promoter and 5′ UTR region of the Fc α receptor (CD89) are not associated with a risk of IgA nephropathy.
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- Journal of Human Genetics, 2001, v. 46, n. 12, p. 694, doi. 10.1007/s100380170002
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- Article
Single-nucleotide polymorphisms of the proprotein convertase subtilisin/kexin type 5 (PCSK5) gene.
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- Journal of Human Genetics, 2001, v. 46, n. 12, p. 730, doi. 10.1007/s100380170008
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- Article
Identification of an aberrant type of rearrangement in the T-cell receptor α/δ locus in adult T-cell leukemia.
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- Journal of Human Genetics, 2001, v. 46, n. 12, p. 706, doi. 10.1007/s100380170004
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- Article
Identification of nonsynonymous polymorphisms in the superantigen-coding region of IDDMK[sub 1,2] 22 and a pilot study on the association between IDDMK[sub 1,2] 22 and type 1 diabetes.
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- Journal of Human Genetics, 2001, v. 46, n. 12, p. 712, doi. 10.1007/s100380170005
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- Article
VNTR sequence on human chromosome 11p15 that affects transcriptional activity.
- Published in:
- Journal of Human Genetics, 2001, v. 46, n. 12, p. 717, doi. 10.1007/s100380170006
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- Article
Identification of six novel MYH9 mutations and genotype–phenotype relationships in autosomal dominant macrothrombocytopenia with leukocyte inclusions.
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- Journal of Human Genetics, 2001, v. 46, n. 12, p. 722, doi. 10.1007/s100380170007
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- Article
ABCC6 gene polymorphism associated with variation in plasma lipoproteins.
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- Journal of Human Genetics, 2001, v. 46, n. 12, p. 699, doi. 10.1007/s100380170003
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- Article
Heterozygous 17-bp deletion in the forkhead transcription factor gene, FOXL2, in a Japanese family with blepharophimosis-ptosis-epicanthus inversus syndrome.
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- Journal of Human Genetics, 2001, v. 46, n. 12, p. 733, doi. 10.1007/s100380170009
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- Article
LETTER TO THE EDITOR.
- Published in:
- Journal of Human Genetics, 2001, v. 46, n. 12, p. 737, doi. 10.1007/PL00010919
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- Article