Anticipation in familial intracranial aneurysms in consecutive generations.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 10, p. 737, doi. 10.1038/sj.ejhg.5201039
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- Publication type:
- Article
Works matching IS 10184813 AND DT 2003 AND VI 11 AND IP 10
Results: 14
1
2
From surnames to the history of Y chromosomes: the Sardinian population as a paradigm.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 10, p. 802, doi. 10.1038/sj.ejhg.5201040
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- Article
3
Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 10, p. 744, doi. 10.1038/sj.ejhg.5201043
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- Publication type:
- Article
4
Analysis of the French National Registry of unrelated bone marrow donors, using surnames as a tool for improving geographical localisation of HLA haplotypes.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 10, p. 794, doi. 10.1038/sj.ejhg.5201038
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- Publication type:
- Article
5
DFNB39, a recessive form of sensorineural hearing impairment, maps to chromosome 7q11.22-q21.12.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 10, p. 812, doi. 10.1038/sj.ejhg.5201041
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- Publication type:
- Article
6
Global survey of haplotype frequencies and linkage disequilibrium at the RET locus.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 10, p. 760, doi. 10.1038/sj.ejhg.5201036
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- Publication type:
- Article
7
Risk communication strategies: state of the art and effectiveness in the context of cancer genetic services.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 10, p. 725, doi. 10.1038/sj.ejhg.5201037
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- Publication type:
- Article
8
DFNB40, a recessive form of sensorineural hearing loss, maps to chromosome 22q11.21-12.1.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 10, p. 816, doi. 10.1038/sj.ejhg.5201045
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- Publication type:
- Article
9
Cell death triggered by a novel mutation in the alphaA-crystallin gene underlies autosomal dominant cataract linked to chromosome 21q.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 10, p. 784, doi. 10.1038/sj.ejhg.5201046
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- Publication type:
- Article
10
Class II neocentromeres: a putative common neocentromere site in band 4q21.2.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 10, p. 749, doi. 10.1038/sj.ejhg.5201047
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- Publication type:
- Article
11
Linear increase of structural and numerical chromosome 9 abnormalities in human sperm regarding age.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 10, p. 754, doi. 10.1038/sj.ejhg.5201049
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- Publication type:
- Article
12
Parametric and nonparametric genome scan analyses for human handedness.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 10, p. 779, doi. 10.1038/sj.ejhg.5201048
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- Publication type:
- Article
13
Portuguese families with dentatorubropallidoluysian atrophy (DRPLA) share a common haplotype of Asian origin.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 10, p. 808, doi. 10.1038/sj.ejhg.5201054
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- Publication type:
- Article
14
Homozygosity mapping of Marinesco-Sjögren syndrome to 5q31.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 10, p. 770, doi. 10.1038/sj.ejhg.5201068
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- Publication type:
- Article