Sib-pairs in multifactorial disorders: the sib-similarity problem.
- Published in:
- Clinical Genetics, 2003, v. 63, n. 1, p. 1, doi. 10.1034/j.1399-0004.2003.630101.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 2003 AND VI 63 AND IP 1
Results: 16
1
2
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.
- Published in:
- Clinical Genetics, 2003, v. 63, n. 1, p. 59, doi. 10.1034/j.1399-0004.2003.630109.x
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- Publication type:
- Article
3
Hotspots.
- Published in:
- Clinical Genetics, 2003, v. 63, n. 1, p. 13, doi. 10.1034/j.1399-0004.2002.6105023.x
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- Publication type:
- Article
4
A predominant increase in the APC gene isoform with exon 9a in a case of attenuated familial adenomatous polyposis.
- Published in:
- Clinical Genetics, 2003, v. 63, n. 1, p. 71, doi. 10.1034/j.1399-0004.2003.630111.x
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- Publication type:
- Article
5
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.
- Published in:
- Clinical Genetics, 2003, v. 63, n. 1, p. 19, doi. 10.1034/j.1399-0004.2003.630104.x
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- Publication type:
- Article
6
Hotspots.
- Published in:
- Clinical Genetics, 2003, v. 63, n. 1, p. 11, doi. 10.1034/j.1399-0004.2002.6105022.x
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- Publication type:
- Article
7
PROMM and deafness: exclusion of ZNF9 as the disease gene in DFNA18 suggests a polygenic origin of the PROMM/DM2 phenotype.
- Published in:
- Clinical Genetics, 2003, v. 63, n. 1, p. 73, doi. 10.1034/j.1399-0004.2003.630112.x
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- Publication type:
- Article
8
Fabry disease: a functional and anatomical study of cardiac manifestations in 20 hemizygous male patients.
- Published in:
- Clinical Genetics, 2003, v. 63, n. 1, p. 46, doi. 10.1034/j.1399-0004.2003.630107.x
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- Publication type:
- Article
9
Genetic technologies, health care policy and the patent bargain.
- Published in:
- Clinical Genetics, 2003, v. 63, n. 1, p. 15, doi. 10.1034/j.1399-0004.2003.630103.x
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- Publication type:
- Article
10
Very low incidence of microsatellite instability in rectal cancers from families at risk for HNPCC.
- Published in:
- Clinical Genetics, 2003, v. 63, n. 1, p. 64, doi. 10.1034/j.1399-0004.2003.630110.x
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- Publication type:
- Article
11
The association of cholesteryl ester transfer protein polymorphism with high-density lipoprotein cholesterol and coronary artery disease in Koreans.
- Published in:
- Clinical Genetics, 2003, v. 63, n. 1, p. 31, doi. 10.1034/j.1399-0004.2003.630105.x
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- Publication type:
- Article
12
A second kindred linked to DFNA20 (17q25.3) reduces the genetic interval.
- Published in:
- Clinical Genetics, 2003, v. 63, n. 1, p. 39, doi. 10.1034/j.1399-0004.2003.630106.x
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- Publication type:
- Article
13
Polymorphisms at the SRBI locus are associated with lipoprotein levels in subjects with heterozygous familial hypercholesterolemia.
- Published in:
- Clinical Genetics, 2003, v. 63, n. 1, p. 53, doi. 10.1034/j.1399-0004.2003.630108.x
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- Publication type:
- Article
14
A case of de novo distal duplication of chromosome 15.
- Published in:
- Clinical Genetics, 2003, v. 63, n. 1, p. 76, doi. 10.1034/j.1399-0004.2003.630113.x
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- Publication type:
- Article
15
“GENETICS AND HEALTH CARE”.
- Published in:
- Clinical Genetics, 2003, v. 63, n. 1, p. 82, doi. 10.1034/j.1399-0004.2003.t01-1-630114.x
- Publication type:
- Article
16
‘Severe’ Prader–Willi syndrome with a large deletion of chromosome 15 due to an unbalanced t(15,22)(q14;q11.2) translocation.
- Published in:
- Clinical Genetics, 2003, v. 63, n. 1, p. 79, doi. 10.1034/j.1399-0004.2003.630114.x
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- Publication type:
- Article