A germline mutation of the KIF1Bβ gene on 1p36 in a family with neural and nonneural tumors.
- Published in:
- Human Genetics, 2008, v. 124, n. 3, p. 279, doi. 10.1007/s00439-008-0553-1
- By:
- Publication type:
- Article
Works matching IS 03406717 AND DT 2008 AND VI 124 AND IP 3
Results: 14
1
2
Association of Interleukin-1 gene polymorphisms with central obesity and metabolic syndrome in a coronary heart disease population.
- Published in:
- Human Genetics, 2008, v. 124, n. 3, p. 199, doi. 10.1007/s00439-008-0540-6
- By:
- Publication type:
- Article
3
Genome-wide distribution of ancestry in Mexican Americans.
- Published in:
- Human Genetics, 2008, v. 124, n. 3, p. 207, doi. 10.1007/s00439-008-0541-5
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- Publication type:
- Article
4
Germline BRCA1 mutations predispose to pancreatic adenocarcinoma.
- Published in:
- Human Genetics, 2008, v. 124, n. 3, p. 271, doi. 10.1007/s00439-008-0554-0
- By:
- Publication type:
- Article
5
Sequence variants in the PLEKHH2 region are associated with diabetic nephropathy in the GoKinD study population.
- Published in:
- Human Genetics, 2008, v. 124, n. 3, p. 255, doi. 10.1007/s00439-008-0548-y
- By:
- Publication type:
- Article
6
LRRK2 R1628P increases risk of Parkinson’s disease: replication evidence.
- Published in:
- Human Genetics, 2008, v. 124, n. 3, p. 287, doi. 10.1007/s00439-008-0544-2
- By:
- Publication type:
- Article
7
Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndrome.
- Published in:
- Human Genetics, 2008, v. 124, n. 3, p. 215, doi. 10.1007/s00439-008-0543-3
- By:
- Publication type:
- Article
8
Jan A. Witkowski and John R. Inglis (eds): Davenport’s dream. Twenty-first century reflections on heredity and eugenics.
- Published in:
- 2008
- By:
- Publication type:
- Book Review
9
Merlin G. Butler, Philip D. K. Lee, Barbara Y. Whitman: Management of Prader-Willi syndrome.
- Published in:
- 2008
- By:
- Publication type:
- Book Review
10
Genetic regulation of amniotic fluid TNF-alpha and soluble TNF receptor concentrations affected by race and preterm birth.
- Published in:
- Human Genetics, 2008, v. 124, n. 3, p. 243, doi. 10.1007/s00439-008-0547-z
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- Publication type:
- Article
11
Network-based model weighting to detect multiple loci influencing complex diseases.
- Published in:
- Human Genetics, 2008, v. 124, n. 3, p. 225, doi. 10.1007/s00439-008-0545-1
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- Publication type:
- Article
12
Gender influences monoallelic expression of ATP10A in human brain.
- Published in:
- Human Genetics, 2008, v. 124, n. 3, p. 235, doi. 10.1007/s00439-008-0546-0
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- Publication type:
- Article
13
Novel human pathological mutations.
- Published in:
- Human Genetics, 2008, v. 124, n. 3, p. 293, doi. 10.1007/s00439-008-0551-3
- Publication type:
- Article
14
Association of PARL rs3732581 genetic variant with insulin levels, metabolic syndrome and coronary artery disease.
- Published in:
- Human Genetics, 2008, v. 124, n. 3, p. 263, doi. 10.1007/s00439-008-0552-2
- By:
- Publication type:
- Article