Found: 11
Select item for more details and to access through your institution.
A three-allelic polymorphic system in exon 12 of the LDL receptor gene is highly informative for segregation analysis of familial hypercholesterolemia in the Spanish population.
- Published in:
- Clinical Genetics, 1996, v. 50, n. 1, p. 50, doi. 10.1111/j.1399-0004.1996.tb02346.x
- By:
- Publication type:
- Article
Short Report on DNA Marker at Candidate Locus.
- Published in:
- Clinical Genetics, 1996, v. 50, n. 1, p. 54, doi. 10.1111/j.1399-0004.1996.tb02347.x
- By:
- Publication type:
- Article
Deciduous teeth in tuberous sclerosis.
- Published in:
- Clinical Genetics, 1996, v. 50, n. 1, p. 36, doi. 10.1111/j.1399-0004.1996.tb02343.x
- By:
- Publication type:
- Article
UICC Symposium on Familial Cancer and Prevention Molecular Epidemiology: a New Strategy toward Cancer Control.
- Published in:
- Clinical Genetics, 1996, v. 50, n. 1, p. 56, doi. 10.1111/j.1399-0004.1996.tb02348.x
- Publication type:
- Article
Presymptomatic molecular diagnosis of autosomal dominant polycystic kidney disease using PKD1-and PKD2-linked markers in Cypriot families.
- Published in:
- Clinical Genetics, 1996, v. 50, n. 1, p. 10, doi. 10.1111/j.1399-0004.1996.tb02339.x
- By:
- Publication type:
- Article
High levels of Lp(a) lipoprotein in a family ith cases of severe pre-eclampsia.
- Published in:
- Clinical Genetics, 1996, v. 50, n. 1, p. 47, doi. 10.1111/j.1399-0004.1996.tb02345.x
- By:
- Publication type:
- Article
Prenatal cystic fibrosis screening in a low-risk population undergoing chorionic villus sampling for fetal karyotyping.
- Published in:
- Clinical Genetics, 1996, v. 50, n. 1, p. 23, doi. 10.1111/j.1399-0004.1996.tb02341.x
- By:
- Publication type:
- Article
Seven DNA polymorphisms in the LDL receptor gene: application to the study of familial hypercholesterolemia in Spain.
- Published in:
- Clinical Genetics, 1996, v. 50, n. 1, p. 28, doi. 10.1111/j.1399-0004.1996.tb02342.x
- By:
- Publication type:
- Article
Parental origin and mechanisms of formation of three eases of 12p tetrasomy.
- Published in:
- Clinical Genetics, 1996, v. 50, n. 1, p. 41, doi. 10.1111/j.1399-0004.1996.tb02344.x
- By:
- Publication type:
- Article
On two patients with and without the classical Wolf-Hirschhorn syndrome (WHS) sharing the same chromosome 4p16.3 specific probe deletion: evidence of a contiguous gene deletion syndrome.
- Published in:
- Clinical Genetics, 1996, v. 50, n. 1, p. 19, doi. 10.1111/j.1399-0004.1996.tb02340.x
- By:
- Publication type:
- Article
Genetic contributions to LDL-C, Apo-B and LDL-C/Apo-B ratio in a sample of Israeli offspring with a parental history of myocardial infarction.
- Published in:
- Clinical Genetics, 1996, v. 50, n. 1, p. 1, doi. 10.1111/j.1399-0004.1996.tb02338.x
- By:
- Publication type:
- Article