Works matching IS 03406717 AND DT 2004 AND VI 114 AND IP 3
Results: 19
Haplotype mapping of the bronchiolitis susceptibility locus near IL8.
- Published in:
- Human Genetics, 2004, v. 114, n. 3, p. 272, doi. 10.1007/s00439-003-1038-x
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- Article
Apolipoprotein B-100 XbaI gene polymorphism in gallbladder cancer.
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- Human Genetics, 2004, v. 114, n. 3, p. 280, doi. 10.1007/s00439-003-1056-8
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- Article
Confirmation of chromosome 7q11 locus for predisposition to intracranial aneurysm.
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- Human Genetics, 2004, v. 114, n. 3, p. 250, doi. 10.1007/s00439-003-1044-z
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- Article
Analysis of heat-shock protein 70 gene polymorphisms and the risk of Parkinson’s disease.
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- Human Genetics, 2004, v. 114, n. 3, p. 236, doi. 10.1007/s00439-003-1050-1
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- Article
Bronya J.B. Keats, Arthur N. Popper, Richard R. Fay (Editors) Springer handbook of auditory research: genetics and auditory disorders: Springer-Verlag, Berlin Heidelberg New York (2002), ISBN 0-387-98501-8, hardcover, 149.00 Euro, £140.50, 129.00 US$
- Published in:
- 2004
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- Publication type:
- Book Review
Novel compound heterozygous mutations in SLC5A2 are responsible for autosomal recessive renal glucosuria.
- Published in:
- Human Genetics, 2004, v. 114, n. 3, p. 314, doi. 10.1007/s00439-003-1054-x
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- Article
Update on the genetics of migraine.
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- Human Genetics, 2004, v. 114, n. 3, p. 225, doi. 10.1007/s00439-003-1055-9
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- Article
Genetic and clinical mosaicism in a patient with neurofibromatosis type 1.
- Published in:
- Human Genetics, 2004, v. 114, n. 3, p. 284, doi. 10.1007/s00439-003-1047-9
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- Article
Genetics and genomics of neurobehavioral disorders: Gene S. Fisch (Editor), Humana Press, ISBN 1-58829-045-X, hardcover, 428 pages, 125.00 US$.
- Published in:
- 2004
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- Publication type:
- Book Review
Members of the CDY family have different expression patterns: CDY1 transcripts have the best correlation with complete spermatogenesis.
- Published in:
- 2004
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- Publication type:
- Erratum
Acknowledgement to referees 2003.
- Published in:
- Human Genetics, 2004, v. 114, n. 3, p. 323, doi. 10.1007/s00439-003-1078-2
- Publication type:
- Article
Public Health Genetics.
- Published in:
- Human Genetics, 2004, v. 114, n. 3, p. 326, doi. 10.1007/s00439-004-1085-y
- Publication type:
- Article
Small deletions disturb desmin architecture leading to breakdown of muscle cells and development of skeletal or cardioskeletal myopathy.
- Published in:
- Human Genetics, 2004, v. 114, n. 3, p. 306, doi. 10.1007/s00439-003-1057-7
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- Article
Mexican American ancestry-informative markers: examination of population structure and marker characteristics in European Americans, Mexican Americans, Amerindians and Asians.
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- Human Genetics, 2004, v. 114, n. 3, p. 263, doi. 10.1007/s00439-003-1058-6
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- Publication type:
- Article
Modulation of penetrance by the wild-type allele in dominantly inherited erythropoietic protoporphyria and acute hepatic porphyrias.
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- Human Genetics, 2004, v. 114, n. 3, p. 256, doi. 10.1007/s00439-003-1059-5
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- Article
G. Bates, P. Harper, L. Jones (eds): Huntington’s Disease, Third Edition: Oxford Monographs on Medical Genetics 45, Oxford University Press, 2002, hardcover, 558 pp (ISBN 0-19-851060-8) £75.00.
- Published in:
- 2004
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- Publication type:
- Book Review
Single cell co-amplification of polymorphic markers for the indirect preimplantation genetic diagnosis of hemophilia A, X-linked adrenoleukodystrophy, X-linked hydrocephalus and incontinentia pigmenti loci on Xq28.
- Published in:
- Human Genetics, 2004, v. 114, n. 3, p. 298, doi. 10.1007/s00439-003-1063-9
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- Publication type:
- Article
Localized aggressive periodontitis is linked to human chromosome 1q25.
- Published in:
- Human Genetics, 2004, v. 114, n. 3, p. 291, doi. 10.1007/s00439-003-1065-7
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- Publication type:
- Article
A novel missense mutation in the paired domain of PAX9 causes non-syndromic oligodontia.
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- Human Genetics, 2004, v. 114, n. 3, p. 242, doi. 10.1007/s00439-003-1066-6
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- Publication type:
- Article