Works matching IS 03406717 AND DT 2002 AND VI 110 AND IP 3
Results: 11
Proposed guidelines for papers describing DNA polymorphism¿disease associations.
- Published in:
- Human Genetics, 2002, v. 110, n. 3, p. 207, doi. 10.1007/s00439-001-0672-4
- Publication type:
- Article
Origin and affinities of indigenous Siberian populations as revealed by HLA class II gene frequencies.
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- Human Genetics, 2002, v. 110, n. 3, p. 209, doi. 10.1007/s00439-001-0668-0
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- Article
CIA30 complex I assembly factor: a candidate for human complex I deficiency?
- Published in:
- Human Genetics, 2002, v. 110, n. 3, p. 264, doi. 10.1007/s00439-001-0673-3
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- Article
A case of segmental paternal isodisomy of chromosome 14.
- Published in:
- Human Genetics, 2002, v. 110, n. 3, p. 251, doi. 10.1007/s00439-002-0688-4
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- Article
Identification of novel mutations in MLC1 responsible for megalencephalic leukoencephalopathy with subcortical cysts.
- Published in:
- Human Genetics, 2002, v. 110, n. 3, p. 279, doi. 10.1007/s00439-002-0682-x
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- Article
Genetic study of SMA patients without homozygous SMN1 deletions: identification of compound heterozygotes and characterisation of novel intragenic SMN1 mutations.
- Published in:
- Human Genetics, 2002, v. 110, n. 3, p. 257, doi. 10.1007/s00439-002-0681-y
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- Publication type:
- Article
A candidate gene for congenital bilateral isolated ptosis identified by molecular analysis of a de novo balanced translocation.
- Published in:
- Human Genetics, 2002, v. 110, n. 3, p. 244, doi. 10.1007/s00439-002-0679-5
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- Article
Genetics of congenital deafness in the Palestinian population: multiple connexin 26 alleles with shared origins in the Middle East.
- Published in:
- Human Genetics, 2002, v. 110, n. 3, p. 284, doi. 10.1007/s00439-001-0674-2
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- Article
Variability of X chromosome inactivation: effect on levels of TIMP1 RNA and role of DNA methylation.
- Published in:
- Human Genetics, 2002, v. 110, n. 3, p. 271, doi. 10.1007/s00439-002-0676-8
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- Publication type:
- Article
Characterisation of interstitial duplications and triplications of chromosome 15q11–q13.
- Published in:
- Human Genetics, 2002, v. 110, n. 3, p. 227, doi. 10.1007/s00439-002-0678-6
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- Publication type:
- Article
Identification and characterization of a novel liver-specific enhancer of the human phenylalanine hydroxylase gene.
- Published in:
- Human Genetics, 2002, v. 110, n. 3, p. 235, doi. 10.1007/s00439-002-0677-7
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- Publication type:
- Article