Works matching IS 03406717 AND DT 2002 AND VI 110 AND IP 1
Results: 17
Critique of "Chromosome 17 and the inducible nitric oxide synthase gene in human essential hypertension"
- Published in:
- Human Genetics, 2002, v. 110, n. 1, p. 98, doi. 10.1007/s00439-001-0641-y
- Publication type:
- Article
A major marker for normal tension glaucoma: association with polymorphisms in the OPA1 gene.
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- Human Genetics, 2002, v. 110, n. 1, p. 52, doi. 10.1007/s00439-001-0645-7
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- Article
Fetal gender determination in early pregnancy through qualitative and quantitative analysis of fetal DNA in maternal serum.
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- Human Genetics, 2002, v. 110, n. 1, p. 75, doi. 10.1007/s00439-001-0649-3
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- Article
Dissecting the epidemiology of a trinucleotide repeat disease – example of FRDA in Finland.
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- Human Genetics, 2002, v. 110, n. 1, p. 36, doi. 10.1007/s00439-001-0642-x
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- Publication type:
- Article
Familial idiopathic basal ganglia calcification (Fahr's disease) without neurological, cognitive and psychiatric symptoms is not linked to the IBGC1 locus on chromosome 14q.
- Published in:
- Human Genetics, 2002, v. 110, n. 1, p. 8, doi. 10.1007/s00439-001-0650-x
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- Article
Mutations in human glycine N-methyltransferase give insights into its role in methionine metabolism.
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- Human Genetics, 2002, v. 110, n. 1, p. 68, doi. 10.1007/s00439-001-0648-4
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- Article
Rate of homologous chromosome bivalents in spermatocytes may predict completion of spermatogenesis in azoospermic men.
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- Human Genetics, 2002, v. 110, n. 1, p. 30, doi. 10.1007/s00439-001-0635-9
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- Article
The USH1C 216G→A mutation and the 9-repeat VNTR(t,t) allele are in complete linkage disequilibrium in the Acadian population.
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- Human Genetics, 2002, v. 110, n. 1, p. 95, doi. 10.1007/s00439-001-0653-7
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- Article
Cytogenetic mapping of a novel locus for type II Waardenburg syndrome.
- Published in:
- Human Genetics, 2002, v. 110, n. 1, p. 64, doi. 10.1007/s00439-001-0643-9
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- Article
Authors response to: Critique of "Chromosome 17 and inducible nitric oxide synthase gene in human essential hypertension" by Rutherford et al. in Human Genetics published on-line September 2001.
- Published in:
- Human Genetics, 2002, v. 110, n. 1, p. 100, doi. 10.1007/s00439-001-0658-2
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- Article
Investigation of the functional effect of monoamine oxidase polymorphisms in human brain.
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- Human Genetics, 2002, v. 110, n. 1, p. 1, doi. 10.1007/s00439-001-0652-8
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- Publication type:
- Article
Paraoxonase gene Gln192Arg (Q192R) polymorphism is associated with coronary artery spasm.
- Published in:
- Human Genetics, 2002, v. 110, n. 1, p. 89, doi. 10.1007/s00439-001-0654-6
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- Publication type:
- Article
Three major lineages of Asian Y chromosomes: implications for the peopling of east and southeast Asia.
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- Human Genetics, 2002, v. 110, n. 1, p. 80, doi. 10.1007/s00439-001-0651-9
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- Publication type:
- Article
Genetic variations in the cholesteryl ester transfer protein gene and high density lipoprotein cholesterol levels in Taiwanese Chinese.
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- Human Genetics, 2002, v. 110, n. 1, p. 57, doi. 10.1007/s00439-001-0640-z
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- Article
Laminin 5 mutations in junctional epidermolysis bullosa: molecular basis of Herlitz vs non-Herlitz phenotypes.
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- Human Genetics, 2002, v. 110, n. 1, p. 41, doi. 10.1007/s00439-001-0630-1
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- Publication type:
- Article
The mutation spectrum of the facilitative glucose transporter gene SLC2A2 (GLUT2) in patients with Fanconi-Bickel syndrome.
- Published in:
- Human Genetics, 2002, v. 110, n. 1, p. 21, doi. 10.1007/s00439-001-0638-6
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- Publication type:
- Article
Linkage disequilibrium between GABRB3 gene and nonsyndromic familial cleft lip with or without cleft palate.
- Published in:
- Human Genetics, 2002, v. 110, n. 1, p. 15, doi. 10.1007/s00439-001-0639-5
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- Publication type:
- Article