Works matching IS 00099163 AND DT 2000 AND VI 58 AND IP 4
Results: 17
Single nucleotide polymorphisms and the future of genetic epidemiology.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 4, p. 250, doi. 10.1034/j.1399-0004.2000.580402.x
- By:
- Publication type:
- Article
Microbubbles used to ‘pop’ new gene into the heart.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 4, p. 269, doi. 10.1034/j.1399-0004.2000.580403.3.x
- By:
- Publication type:
- Article
Pedigree parables.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 4, p. 241, doi. 10.1034/j.1399-0004.2000.580401.x
- By:
- Publication type:
- Article
Repairing the genomic defect in muscular dystrophy.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 4, p. 265, doi. 10.1034/j.1399-0004.2000.580403.1.x
- By:
- Publication type:
- Article
Shedding new light on the pathogenesis of familial Alzheimer disease.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 4, p. 266, doi. 10.1034/j.1399-0004.2000.580403.2.x
- By:
- Publication type:
- Article
Collagens: building blocks at the end of the development line.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 4, p. 270, doi. 10.1034/j.1399-0004.2000.580404.x
- By:
- Publication type:
- Article
Low density lipoprotein receptor-related protein gene polymorphisms and risk for late-onset Alzheimer's disease in a Japanese population.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 4, p. 319, doi. 10.1034/j.1399-0004.2000.580410.x
- By:
- Publication type:
- Article
Genetic landmarks through philately – Barbara McClintock.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 4, p. 280, doi. 10.1034/j.1399-0004.2000.580405.x
- By:
- Publication type:
- Article
Linkage exclusion and mutational analysis of the noggin gene in patients with fibrodysplasia ossificans progressiva (FOP).
- Published in:
- Clinical Genetics, 2000, v. 58, n. 4, p. 291, doi. 10.1034/j.1399-0004.2000.580407.x
- By:
- Publication type:
- Article
A preliminary validation of a family history assessment form to select women at risk for breast or ovarian cancer for referral to a genetics center.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 4, p. 299, doi. 10.1034/j.1399-0004.2000.580408.x
- By:
- Publication type:
- Article
Optimization of the fluorescence in situ hybridization (FISH) technique for high detection efficiency of very small proportions of target interphase nuclei.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 4, p. 309, doi. 10.1034/j.1399-0004.2000.580409.x
- By:
- Publication type:
- Article
Familial t(6;21)(p21.1;p13) translocation associated with male-only sterility.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 4, p. 324, doi. 10.1034/j.1399-0004.2000.580411.x
- By:
- Publication type:
- Article
Imprinting centre deletions in two PWS families: implications for diagnostic testing and genetic counselling.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 4, p. 284, doi. 10.1034/j.1399-0004.2000.580406.x
- By:
- Publication type:
- Article
Linkage and candidate gene analysis of autosomal-dominant familial exudative vitreoretinopathy.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 4, p. 329, doi. 10.1034/j.1399-0004.2000.580412.x
- By:
- Publication type:
- Article
The incidence of cystic fibrosis (CF) mutations among patients from Croatia.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 4, p. 333, doi. 10.1034/j.1399-0004.2000.580413.x
- By:
- Publication type:
- Article
Clitoris and labia minora agenesis – an undescribed malformation.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 4, p. 336, doi. 10.1034/j.1399-0004.2000.580414.x
- By:
- Publication type:
- Article
Determination of the frequency of the 35delG allele in Brazilian neonates.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 4, p. 339, doi. 10.1034/j.1399-0004.2000.580415.x
- By:
- Publication type:
- Article