|
Editorial
Reviews Ethical Issues in Molecular Screening for Heterozygous Familial Hypercholesterolemia: The Complexity of Dealing with Genetic Susceptibility to Coronary Artery Disease Daniel Gaudet, Claude Gagné, Patrice Perron, Patrick Couture, Serena Tonstad
Prenatal Screening and the Reduction of Birth Defects in Populations Patricia A. Baird
Original Papers Down Syndrome and Parity M. Clementi, S. Bianca, F. Benedicenti, R. Tenconi
Analysis of the Population Structure in Oman Anna Rajab, Michael A. Patton
Screening for Alpha-Thalassemia-1 Heterozygotes in Expecting Couples by the Combination of a Simple Erythrocyte Osmotic Fragility Test and a PCR-Based Method Torpong Sanguansermsri, Nonglak Phumyu, Surasit Chomchuen, Heinrich F.Steger
Genetic, Epidemiologic and Social Features of Colour Blindness A. Tagarelli, A. Piro, G. Tagarelli
Study of 290 Cases of Polyhydramnios and Congenital Malformations in a Series of 225,669 Consecutive Births Claude G. Stoll, Marie-Paule Roth, Béatrice Dott, Yves Alembik
Commentaries The UK's Policies on Genetic Testing for Late-Onset Disorders Neil A. Holtzman
Commissioning Clinical Genetic Services in the UK H. Kääriäinen
Letters to the Editor Development and Use of a National Haemoglobinopathy Register in Oman Anna Rajab, Michael A. Patton
Screening for Female Fragile X Premutation and Full Mutation Carriers Maria Isabel Tejada, Mercedes Duran
|
|