Works matching IS 00099163 AND DT 2003 AND VI 63 AND IP 1
Results: 16
Sib-pairs in multifactorial disorders: the sib-similarity problem.
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- Clinical Genetics, 2003, v. 63, n. 1, p. 1, doi. 10.1034/j.1399-0004.2003.630101.x
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- Article
Hotspots.
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- Clinical Genetics, 2003, v. 63, n. 1, p. 11, doi. 10.1034/j.1399-0004.2002.6105022.x
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- Article
Hotspots.
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- Clinical Genetics, 2003, v. 63, n. 1, p. 13, doi. 10.1034/j.1399-0004.2002.6105023.x
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- Article
Genetic technologies, health care policy and the patent bargain.
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- Clinical Genetics, 2003, v. 63, n. 1, p. 15, doi. 10.1034/j.1399-0004.2003.630103.x
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- Article
The TaqIB and -629C>A polymorphisms at the cholesteryl ester transfer protein locus: associations with lipid levels in a multiethnic population. The 1998 Singapore National Health Survey.
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- Clinical Genetics, 2003, v. 63, n. 1, p. 19, doi. 10.1034/j.1399-0004.2003.630104.x
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- Article
The association of cholesteryl ester transfer protein polymorphism with high-density lipoprotein cholesterol and coronary artery disease in Koreans.
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- Clinical Genetics, 2003, v. 63, n. 1, p. 31, doi. 10.1034/j.1399-0004.2003.630105.x
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- Article
A second kindred linked to DFNA20 (17q25.3) reduces the genetic interval.
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- Clinical Genetics, 2003, v. 63, n. 1, p. 39, doi. 10.1034/j.1399-0004.2003.630106.x
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- Article
Fabry disease: a functional and anatomical study of cardiac manifestations in 20 hemizygous male patients.
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- Clinical Genetics, 2003, v. 63, n. 1, p. 46, doi. 10.1034/j.1399-0004.2003.630107.x
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- Article
Polymorphisms at the SRBI locus are associated with lipoprotein levels in subjects with heterozygous familial hypercholesterolemia.
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- Clinical Genetics, 2003, v. 63, n. 1, p. 53, doi. 10.1034/j.1399-0004.2003.630108.x
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- Article
A novel point mutation of the androgen receptor (F804L) in an Egyptian newborn with complete androgen insensitivity associated with congenital glaucoma and hypertrophic pyloric stenosis.
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- Clinical Genetics, 2003, v. 63, n. 1, p. 59, doi. 10.1034/j.1399-0004.2003.630109.x
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Very low incidence of microsatellite instability in rectal cancers from families at risk for HNPCC.
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- Clinical Genetics, 2003, v. 63, n. 1, p. 64, doi. 10.1034/j.1399-0004.2003.630110.x
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- Article
A predominant increase in the APC gene isoform with exon 9a in a case of attenuated familial adenomatous polyposis.
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- Clinical Genetics, 2003, v. 63, n. 1, p. 71, doi. 10.1034/j.1399-0004.2003.630111.x
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- Article
PROMM and deafness: exclusion of ZNF9 as the disease gene in DFNA18 suggests a polygenic origin of the PROMM/DM2 phenotype.
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- Clinical Genetics, 2003, v. 63, n. 1, p. 73, doi. 10.1034/j.1399-0004.2003.630112.x
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- Article
A case of de novo distal duplication of chromosome 15.
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- Clinical Genetics, 2003, v. 63, n. 1, p. 76, doi. 10.1034/j.1399-0004.2003.630113.x
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- Article
‘Severe’ Prader–Willi syndrome with a large deletion of chromosome 15 due to an unbalanced t(15,22)(q14;q11.2) translocation.
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- Clinical Genetics, 2003, v. 63, n. 1, p. 79, doi. 10.1034/j.1399-0004.2003.630114.x
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“GENETICS AND HEALTH CARE”.
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- Clinical Genetics, 2003, v. 63, n. 1, p. 82, doi. 10.1034/j.1399-0004.2003.t01-1-630114.x
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- Article