Clinical Genetics

Hotspots
pp. 191-195(5)
Authors: Mittal B.; Pandey U.

Novel neuropeptide Y1 and Y5 receptor gene variants: associations with serum triglyceride and high-density lipoprotein cholesterol levels
pp. 196-202(7)
Authors: Blumenthal J.; Andersen R.; Mitchell B.; Seibert M.; Yang H.; Herzog H.; Beamer B.; Franckowiak S.; Walston J.

Genotyping of Israeli infertile men with idiopathic oligozoospermia
pp. 203-207(5)
Authors: Madgar I.; Green L.; Kent-First M.; Weissenberg R.; Gershoni-Baruch R.; Goldman B.; Friedman E.

Genetic polymorphisms of the apolipoprotein A-IV in a Greek population and their relation to plasma lipid and lipoprotein levels
pp. 208-213(6)
Authors: Miltiadous G.; Hatzivassiliou M.; Bashiardes E.; Bairaktari E.; Cariolou M.; Elisaf M.

Bronchomalacia associated with pulmonary atresia, ventricular septal defect and major aortopulmonary collateral arteries, and chromosome 22q11.2 deletion
pp. 214-219(6)
Authors: Yamagishi H.; Maeda J.; Higuchi M.; Katada Y.; Yamagishi C.; Matsuo N.; Kojima Y.

Sibship stability of genotype and phenotype in myotonic dystrophy
pp. 220-225(6)
Authors: Brisson D.; Tremblay M.; Prévost C.; Laberge C.; Puymirat J.; Mathieu J.

ATP binding cassette G5 C1950G polymorphism may affect blood cholesterol concentrations in humans
pp. 226-229(4)
Authors: Weggemans R.; Zock P.; Tai E.; Ordovas J.; Molhuizen H.; Katan M.

Developing a quality scoring system for epidemiological surveys of genetic disorders
pp. 230-234(5)
Authors: Al-Jader L.; Newcombe R.; Hayes S.; Murray A.; Layzell J.; Harper P.

Lack of association between methylenetetrahydrofolate reductase (MTHFR) C677T and ischaemic heart disease (IHD): family-based association study in a Spanish population
pp. 235-239(5)
Authors: González-Pérez E.; Via M.; López-Alomar A.; Esteban E.; Valveny N.; Bao M.; Domingo E.; Moral P.

Apolipoprotein molecular variation in Moroccan Berbers: pentanucleotide (TTTTA)n repeat in the LPA gene and APOE-C1-C2 gene cluster
pp. 240-244(5)
Authors: Harich N.; Esteban E.; López-Alomar A.; Chafik A.; Moral P.

Comparison of two different protocols of neonatal screening for cystic fibrosis
pp. 245-249(5)
Authors: Narzi L.; Lucarelli M.; Lelli A.; Grandoni F.; Lo Cicero S.; Ferraro A.; Matarazzo P.; Delaroche I.; Quattrucci S.; Strom R.; Antonelli M.

Normal levels of soluble transferrin receptor in Friedreich ataxia
pp. 250-251(2)

Familial hypocalciuric hypercalcaemia in a large family with neurofibromatosis 1
pp. 252-254(3)

A novel mutation (N32K) of GLUT2 gene in a Japanese patient with Fanconi–Bickel syndrome
pp. 255-256(2)