Works matching IS 10184813 AND DT 2000 AND VI 8 AND IP 5
Results: 14
Microdissection of chromosome 2 – between-arm intrachromosomal insertion.
- Published in:
- European Journal of Human Genetics, 2000, v. 8, n. 5, p. 393, doi. 10.1038/sj.ejhg.5200421
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- Article
Positional cloning and characterisation of the human DLGAP2 gene and its exclusion in progressive epilepsy with mental retardation.
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- European Journal of Human Genetics, 2000, v. 8, n. 5, p. 381, doi. 10.1038/sj.ejhg.5200440
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- Article
Novel mutations in the duplicated region of PKD1 gene.
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- European Journal of Human Genetics, 2000, v. 8, n. 5, p. 353, doi. 10.1038/sj.ejhg.5200459
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- Article
Narrowing the Duane syndrome critical region at chromosome 8q13 down to 40 kb.
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- European Journal of Human Genetics, 2000, v. 8, n. 5, p. 319, doi. 10.1038/sj.ejhg.5200461
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- Article
Importance of searching for associated mitochondrial DNA alterations in patients with multiple deletions.
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- European Journal of Human Genetics, 2000, v. 8, n. 5, p. 331, doi. 10.1038/sj.ejhg.5200463
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- Article
Genetic structure of north-west Africa revealed by STR analysis.
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- European Journal of Human Genetics, 2000, v. 8, n. 5, p. 360, doi. 10.1038/sj.ejhg.5200464
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- Article
Haemochromatosis gene mutations and risk of coronary artery disease.
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- European Journal of Human Genetics, 2000, v. 8, n. 5, p. 389, doi. 10.1038/sj.ejhg.5200465
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- Article
Book Review.
- Published in:
- 2000
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- Publication type:
- Book Review
MtDNA and Y chromosome polymorphisms in Hungary: inferences from the palaeolithic, neolithic and Uralic influences on the modern Hungarian gene pool.
- Published in:
- European Journal of Human Genetics, 2000, v. 8, n. 5, p. 339, doi. 10.1038/sj.ejhg.5200468
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- Article
No evidence for the involvement of CAG/CTG repeats from within 18q21.33–q23 in bipolar disorder.
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- European Journal of Human Genetics, 2000, v. 8, n. 5, p. 385, doi. 10.1038/sj.ejhg.5200469
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- Article
Lack of Hardy-Weinberg equilibrium for the most prevalent PMM2 mutation in CDG-Ia (congenital disorders of glycosylation type Ia).
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- European Journal of Human Genetics, 2000, v. 8, n. 5, p. 367, doi. 10.1038/sj.ejhg.5200470
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- Article
Clouston hidrotic ectodermal dysplasia (HED): genetic homogeneity, presence of a founder effect in the French Canadian population and fine genetic mapping.
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- European Journal of Human Genetics, 2000, v. 8, n. 5, p. 372, doi. 10.1038/sj.ejhg.5200471
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- Article
Cell type specificity in alternative splicing of the human mismatch repair gene hMSH2.
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- European Journal of Human Genetics, 2000, v. 8, n. 5, p. 347, doi. 10.1038/sj.ejhg.5200472
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- Article
Preserved speech variant is allelic of classic Rett syndrome.
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- European Journal of Human Genetics, 2000, v. 8, n. 5, p. 325, doi. 10.1038/sj.ejhg.5200473
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- Article