U. Eiholzer, D. L'Allemand, WB. Zipf (eds): Prader-Willi syndrome as a model for obesity.
- Published in:
- Human Genetics, 2004, v. 114, n. 4, p. 398, doi. 10.1007/s00439-003-1064-8
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- Publication type:
- Article
Works matching IS 03406717 AND DT 2004 AND VI 114 AND IP 4
Results: 16
1
2
David Reiss, Jenae M. Neiderhiser, E. Mavis Hetherington, Robert Plomin (Editors): The relationship code: deciphering genetic and social influences on adolescent development.
- Published in:
- Human Genetics, 2004, v. 114, n. 4, p. 399, doi. 10.1007/s00439-003-1069-3
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- Publication type:
- Article
3
R. Horowoski, Y. Mizuno, C.W. Olanow, W.H. Poewe, P. Riederer, J.A. Stoessl, M.B.H. Youdim (Editors) Advances in research on neurodegeneration (volume 10).
- Published in:
- Human Genetics, 2004, v. 114, n. 4, p. 400, doi. 10.1007/s00439-003-1070-x
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- Publication type:
- Article
4
Contrasting patterns of Y chromosome variation in Ashkenazi Jewish and host non-Jewish European populations.
- Published in:
- Human Genetics, 2004, v. 114, n. 4, p. 354, doi. 10.1007/s00439-003-1073-7
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- Publication type:
- Article
5
A mutation in PCSK9 causing autosomal-dominant hypercholesterolemia in a Utah pedigree.
- Published in:
- Human Genetics, 2004, v. 114, n. 4, p. 349, doi. 10.1007/s00439-003-1071-9
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- Publication type:
- Article
6
Leukotriene-related gene polymorphisms in ASA-intolerant asthma: an association with a haplotype of 5-lipoxygenase.
- Published in:
- Human Genetics, 2004, v. 114, n. 4, p. 337, doi. 10.1007/s00439-004-1082-1
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- Publication type:
- Article
7
Origin and spread of the 1278insTATC mutation causing Tay-Sachs disease in Ashkenazi Jews: genetic drift as a robust and parsimonious hypothesis.
- Published in:
- Human Genetics, 2004, v. 114, n. 4, p. 366, doi. 10.1007/s00439-003-1072-8
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- Publication type:
- Article
8
Nucleotide and haplotypic diversity of the NOS2A promoter region and its relationship to cerebral malaria.
- Published in:
- Human Genetics, 2004, v. 114, n. 4, p. 401, doi. 10.1007/s00439-003-1068-4
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- Article
9
Mutations.
- Published in:
- Human Genetics, 2004, v. 114, n. 4, p. 402, doi. 10.1007/s00439-004-1090-1
- Publication type:
- Article
10
The assertion that a G21V mutation in AGTR2 causes mental retardation is not supported by other studies.
- Published in:
- Human Genetics, 2004, v. 114, n. 4, p. 396, doi. 10.1007/s00439-003-1076-4
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- Publication type:
- Article
11
Genetics of parkin-linked disease.
- Published in:
- Human Genetics, 2004, v. 114, n. 4, p. 327, doi. 10.1007/s00439-003-1074-6
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- Publication type:
- Article
12
AGTR2 mutation and mental retardation: a reply.
- Published in:
- Human Genetics, 2004, v. 114, n. 4, p. 397, doi. 10.1007/s00439-003-1077-3
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- Publication type:
- Article
13
Novel SBDS mutations caused by gene conversion in Japanese patients with Shwachman-Diamond syndrome.
- Published in:
- Human Genetics, 2004, v. 114, n. 4, p. 345
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- Publication type:
- Article
14
TP53 haplotype-based analysis and incidence of post-angioplasty restenosis.
- Published in:
- Human Genetics, 2004, v. 114, n. 4, p. 386, doi. 10.1007/s00439-003-1080-8
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- Publication type:
- Article
15
Patterns of linkage disequilibrium in the MHC region on human chromosome 6p.
- Published in:
- Human Genetics, 2004, v. 114, n. 4, p. 377, doi. 10.1007/s00439-003-1075-5
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- Publication type:
- Article
16
Common variants within the interleukin 4 receptor a gene (IL4R) are associated with susceptibility to osteoarthritis.
- Published in:
- Human Genetics, 2004, v. 114, n. 4, p. 391, doi. 10.1007/s00439-004-1083-0
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- Publication type:
- Article