Consanguinity and its relevance to clinical genetics.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 2, p. 89, doi. 10.1034/j.1399-0004.2001.600201.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 2001 AND VI 60 AND IP 2
Results: 14
1
2
HotSpots.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 2, p. 99, doi. 10.1034/j.1399-0004.2001.6002021.x
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- Publication type:
- Article
3
HotSpots.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 2, p. 100, doi. 10.1034/j.1399-0004.2001.6002022.x
- By:
- Publication type:
- Article
4
HotSpots.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 2, p. 102, doi. 10.1034/j.1399-0004.2001.6002023.x
- By:
- Publication type:
- Article
5
History of genetics through philately – Carl Linnaeus (Carl von Linné).
- Published in:
- Clinical Genetics, 2001, v. 60, n. 2, p. 104, doi. 10.1034/j.1399-0004.2001.600203.x
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- Publication type:
- Article
6
The additive effect of neurotransmitter genes in pathological gambling.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 2, p. 107, doi. 10.1034/j.1399-0004.2001.600204.x
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- Publication type:
- Article
7
Determination of a positive malignant hyperthermia (MH) disposition without the in vitro contracture test in families carrying the RYR1 Arg614Cys mutation.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 2, p. 117, doi. 10.1034/j.1399-0004.2001.600205.x
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- Publication type:
- Article
8
Phenotype variability of two FAP families with an identical APC germline mutation at codon 1465: a potential modifier effect?
- Published in:
- Clinical Genetics, 2001, v. 60, n. 2, p. 125, doi. 10.1034/j.1399-0004.2001.600206.x
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- Publication type:
- Article
9
Apolipoprotein E polymorphism and lipid levels differ by gender and family history of diabetes: the Rancho Bernardo Study.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 2, p. 132, doi. 10.1034/j.1399-0004.2001.600207.x
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- Publication type:
- Article
10
Genetic heterogeneity in Korean families with autosomal-dominant polycystic kidney disease (ADPKD): the first Asian report.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 2, p. 138, doi. 10.1034/j.1399-0004.2001.600208.x
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- Publication type:
- Article
11
Quantification of all fetal nucleated cells in maternal blood between the 18th and 22nd weeks of pregnancy using molecular cytogenetic techniques.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 2, p. 145, doi. 10.1034/j.1399-0004.2001.600209.x
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- Publication type:
- Article
12
PAX6 mutation in a family with aniridia, congenital ptosis, and mental retardation.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 2, p. 151, doi. 10.1034/j.1399-0004.2001.600210.x
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- Publication type:
- Article
13
Further evidence for linkage of low–mid frequency hearing impairment to the candidate region on chromosome 4p16.3.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 2, p. 155, doi. 10.1034/j.1399-0004.2001.600211.x
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- Publication type:
- Article
14
Molecular genetic analysis of the cystathionine β-synthase gene in Portuguese homocystinuria patients: three novel mutations.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 2, p. 161, doi. 10.1034/j.1399-0004.2001.600212.x
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- Publication type:
- Article