Works matching IS 14345161 AND DT 2003 AND VI 48 AND IP 11
Results: 10
The apolipoprotein CIII T2854G variants are associated with postprandial triacylglycerol concentrations in normolipidemic Korean men.
- Published in:
- Journal of Human Genetics, 2003, v. 48, n. 11, p. 551, doi. 10.1007/s10038-003-0074-7
- By:
- Publication type:
- Article
Human endogenous retroviruses with transcriptional potential in the brain.
- Published in:
- Journal of Human Genetics, 2003, v. 48, n. 11, p. 575, doi. 10.1007/s10038-003-0081-8
- By:
- Publication type:
- Article
Different attenuated phenotypes of GM2 gangliosidosis variant B in Japanese patients with HEXA mutations at codon 499, and five novel mutations responsible for infantile acute form.
- Published in:
- Journal of Human Genetics, 2003, v. 48, n. 11, p. 571, doi. 10.1007/s10038-003-0080-9
- By:
- Publication type:
- Article
A family with spinal anaplastic ependymoma: evidence of loss of chromosome 22q in tumor.
- Published in:
- Journal of Human Genetics, 2003, v. 48, n. 11, p. 598, doi. 10.1007/s10038-003-0078-3
- By:
- Publication type:
- Article
Identification and characterization of a novel splice-site mutation in a patient with Wiskott-Aldrich syndrome.
- Published in:
- Journal of Human Genetics, 2003, v. 48, n. 11, p. 590, doi. 10.1007/s10038-003-0083-6
- By:
- Publication type:
- Article
Mutations in the gene encoding KIAA1199 protein, an inner-ear protein expressed in Deiters’ cells and the fibrocytes, as the cause of nonsyndromic hearing loss.
- Published in:
- Journal of Human Genetics, 2003, v. 48, n. 11, p. 564, doi. 10.1007/s10038-003-0079-2
- By:
- Publication type:
- Article
Structural basis of the GM2 gangliosidosis B variant.
- Published in:
- Journal of Human Genetics, 2003, v. 48, n. 11, p. 582, doi. 10.1007/s10038-003-0082-7
- By:
- Publication type:
- Article
Power of association test for detecting minor histocompatibility gene causing graft-versus-host disease following bone marrow transplantation.
- Published in:
- 2003
- By:
- Publication type:
- Correction Notice
Identification of a novel liver-specific expressed gene, TCP10L, encoding a human leucine zipper protein with transcription inhibition activity.
- Published in:
- Journal of Human Genetics, 2003, v. 48, n. 11, p. 556, doi. 10.1007/s10038-003-0075-6
- By:
- Publication type:
- Article
Characterization of six base pair deletion in the putative HNF1-binding site of human PXR promoter.
- Published in:
- Journal of Human Genetics, 2003, v. 48, n. 11, p. 594, doi. 10.1007/s10038-003-0076-5
- By:
- Publication type:
- Article