Works matching IS 03406717 AND DT 2005 AND VI 117 AND IP 1
Results: 13
Genetic evidence in support of a shared Eurasian-North African dairying origin.
- Published in:
- Human Genetics, 2005, v. 117, n. 1, p. 34, doi. 10.1007/s00439-005-1266-3
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- Article
Ancestral origins of the prion protein gene D178N mutation in the Basque Country.
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- Human Genetics, 2005, v. 117, n. 1, p. 61, doi. 10.1007/s00439-005-1277-0
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- Article
Functional promoter polymorphism in theTBX21gene associated with aspirin-induced asthma.
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- Human Genetics, 2005, v. 117, n. 1, p. 16, doi. 10.1007/s00439-005-1285-0
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- Article
AHSGgene variant is associated with leanness among Swedish men.
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- Human Genetics, 2005, v. 117, n. 1, p. 54, doi. 10.1007/s00439-005-1286-z
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- Article
Biochemical characterisation of the proteins encoded by the DiGeorge critical region 6 (DGCR6) genes.
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- Human Genetics, 2005, v. 117, n. 1, p. 70, doi. 10.1007/s00439-005-1267-2
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- Article
Association between the neuron-specific RNA-binding protein ELAVL4 and Parkinson disease.
- Published in:
- Human Genetics, 2005, v. 117, n. 1, p. 27, doi. 10.1007/s00439-005-1259-2
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- Article
Dorian J. Pritchard, Bruce R. Korf (Eds): Medical Genetics at a Glance. Blackwell (2003) ISBN 0632063736, paperback, 120 pages, 48 illustrations, £15.95.
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- 2005
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- Publication type:
- Book Review
A homozygous nonsense mutation inSOX9in the dominant disorder campomelic dysplasia: a case of mitotic gene conversion.
- Published in:
- Human Genetics, 2005, v. 117, n. 1, p. 43, doi. 10.1007/s00439-005-1295-y
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- Article
De novo t(7;10)(q33;q23) translocation and closely juxtaposed microdeletion in a patient with macrocephaly and developmental delay.
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- Human Genetics, 2005, v. 117, n. 1, p. 1, doi. 10.1007/s00439-005-1273-4
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- Article
Identification of deletions and duplications of the DMD gene in affected males and carrier females by multiple ligation probe amplification (MLPA).
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- Human Genetics, 2005, v. 117, n. 1, p. 92, doi. 10.1007/s00439-005-1270-7
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- Article
Gly118Asp is a SCA14 founder mutation in the Dutch ataxia population.
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- Human Genetics, 2005, v. 117, n. 1, p. 88, doi. 10.1007/s00439-005-1278-z
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- Article
Variation inITGB3has sex-specific associations with plasma lipoprotein(a) and whole blood serotonin levels in a population-based sample.
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- Human Genetics, 2005, v. 117, n. 1, p. 81, doi. 10.1007/s00439-004-1250-3
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- Article
Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss.
- Published in:
- Human Genetics, 2005, v. 117, n. 1, p. 9, doi. 10.1007/s00439-005-1276-1
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- Article