Works matching IS 14345161 AND DT 2004 AND VI 49 AND IP 2
Results: 9
Identification of a novel polymorphism involving a CGG repeat in the PTCH gene and a genome-wide screening of CGG-containing genes.
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- Journal of Human Genetics, 2004, v. 49, n. 2, p. 97, doi. 10.1007/s10038-003-0117-0
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3’ rapid amplification of cDNA ends (RACE) walking for rapid structural analysis of large transcripts.
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- Journal of Human Genetics, 2004, v. 49, n. 2, p. 102, doi. 10.1007/s10038-003-0109-0
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- Article
Whole exon 5 and intron 5 replaced by RHCE in D[sup Va](Hus).
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- Journal of Human Genetics, 2004, v. 49, n. 2, p. 106, doi. 10.1007/s10038-003-0112-5
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- Article
Catalog of 162 single nucleotide polymorphisms (SNPs) in a 4.7-kb region of the HLA-DP loci in southern Chinese ethnic groups.
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- Journal of Human Genetics, 2004, v. 49, n. 2, p. 73, doi. 10.1007/s10038-003-0110-7
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- Article
Genetic variants in PCSK9 affect the cholesterol level in Japanese.
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- Journal of Human Genetics, 2004, v. 49, n. 2, p. 109, doi. 10.1007/s10038-003-0114-3
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- Article
High heritability of bone size at the hip and spine in Chinese.
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- Journal of Human Genetics, 2004, v. 49, n. 2, p. 87, doi. 10.1007/s10038-003-0113-4
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- Article
LRP5, low-density-lipoprotein-receptor-related protein 5, is a determinant for bone mineral density.
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- Journal of Human Genetics, 2004, v. 49, n. 2, p. 80, doi. 10.1007/s10038-003-0111-6
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- Article
The chimeric CYP21P/CYP21 gene and 21-hydroxylase deficiency.
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- Journal of Human Genetics, 2004, v. 49, n. 2, p. 65, doi. 10.1007/s10038-003-0115-2
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- Article
Leigh syndrome caused by mitochondrial DNA G13513A mutation: frequency and clinical features in Japan.
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- Journal of Human Genetics, 2004, v. 49, n. 2, p. 92, doi. 10.1007/s10038-003-0116-1
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- Article