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Publications by W Reardon

Medical Genetics: Advances in Brief: Mutations of Low-Density-Lipoprotein-Receptor Gene, Variation in Plasma Cholesterol, and Expression of Coronary Heart Disease in Homozygous Familial Hypercholesterolaemia

Journal of Medical Genetics
Genetics
1993English

Medical Genetics: Advances in Brief: Congenital Bilateral Perisylvian Syndrome: Study of 31 Patients

Journal of Medical Genetics
Genetics
1993English

Medical Genetics: Advances in Brief: Abnormal Expression of Dystrophin-Associated Proteins in Fukuyama-Type Congenital Muscular Dystrophy

Journal of Medical Genetics
Genetics
1993English

Crouzon Syndrome Is Not Linked to Craniosynostosis Loci at 7p and 5qter.

Journal of Medical Genetics
Genetics
1994English

Minimal Expression of Myotonic Dystrophy: A Clinical and Molecular Analysis.

Journal of Medical Genetics
Genetics
1992English

The Natural History of Congenital Myotonic Dystrophy: Mortality and Long Term Clinical Aspects.

Archives of Disease in Childhood
Child HealthPediatricsPerinatology
1993English

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