X-chromosome inactivation in the human trophoblast of early pregnancy.
- Published in:
- Journal of Human Genetics, 2000, v. 45, n. 3, p. 119, doi. 10.1007/s100380050197
- By:
- Publication type:
- Article
Works matching IS 14345161 AND DT 2000 AND VI 45 AND IP 3
Results: 14
1
2
Molecular analysis of α-thalassemia in Nepal: correlation with malaria endemicity.
- Published in:
- Journal of Human Genetics, 2000, v. 45, n. 3, p. 127, doi. 10.1007/s100380050198
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- Publication type:
- Article
3
Identification of Rad51 alteration in patients with bilateral breast cancer.
- Published in:
- Journal of Human Genetics, 2000, v. 45, n. 3, p. 133, doi. 10.1007/s100380050199
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- Publication type:
- Article
4
The 4G/5G polymorphism of the plasminogen activator inhibitor-1 gene is associated with severe preeclampsia.
- Published in:
- Journal of Human Genetics, 2000, v. 45, n. 3, p. 138, doi. 10.1007/s100380050200
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- Publication type:
- Article
5
A Japanese propositus with D-- phenotype characterized by the deletion of both the RHCE gene and D1S80 locus situated in chromosome 1p and the existence of a new CE-D-CE hybrid gene.
- Published in:
- Journal of Human Genetics, 2000, v. 45, n. 3, p. 142, doi. 10.1007/s100380050201
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- Publication type:
- Article
6
Co-segregation of elevated LDL with a novel mutation (D92K) of the LDL receptor in a kindred with multiple lipoprotein abnormalities.
- Published in:
- Journal of Human Genetics, 2000, v. 45, n. 3, p. 154, doi. 10.1007/s100380050202
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- Publication type:
- Article
7
Novel mutations of the FANCG gene causing alternative splicing in Japanese Fanconi anemia.
- Published in:
- Journal of Human Genetics, 2000, v. 45, n. 3, p. 159, doi. 10.1007/s100380050203
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- Publication type:
- Article
8
Genetic alteration of the DCX gene in Japanese patients with subcortical laminar heterotopia or isolated lissencephaly sequence.
- Published in:
- Journal of Human Genetics, 2000, v. 45, n. 3, p. 167
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- Publication type:
- Article
9
Human amniotic epithelial cells are promising transgene carriers for allogeneic cell transplantation into liver.
- Published in:
- Journal of Human Genetics, 2000, v. 45, n. 3, p. 171, doi. 10.1007/s100380050205
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- Publication type:
- Article
10
p24/ING1-ALT1 and p47/ING1-ALT2, distinct alternative transcripts of p33/ING1.
- Published in:
- Journal of Human Genetics, 2000, v. 45, n. 3, p. 177, doi. 10.1007/s100380050206
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- Publication type:
- Article
11
Twenty single nucleotide polymorphisms (SNPs) and their allelic frequencies in four genes that are responsible for familial long QT syndrome in the Japanese population.
- Published in:
- Journal of Human Genetics, 2000, v. 45, n. 3, p. 182, doi. 10.1007/s100380050207
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- Publication type:
- Article
12
Disparity between association and linkage analysis for HNF1A G319S in type 2 diabetes in Canadian Oji-Cree.
- Published in:
- Journal of Human Genetics, 2000, v. 45, n. 3, p. 184, doi. 10.1007/s100380050208
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- Publication type:
- Article
13
Molecular cloning and expression analysis of the human DA41 gene and its mapping to chromosome 9q21.2-q21.3.
- Published in:
- Journal of Human Genetics, 2000, v. 45, n. 3, p. 188, doi. 10.1007/s100380050209
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- Publication type:
- Article
14
cDNA cloning, tissue expression, and chromosome mapping of human homolog of SOX18.
- Published in:
- Journal of Human Genetics, 2000, v. 45, n. 3, p. 192, doi. 10.1007/s100380050210
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- Publication type:
- Article