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Clinical Genetics|April 1, 1992
Transmission of breast cancer--a controversy resolvedL Iselius, M Littler, N Morton
Clinical Genetics|May 21, 2004
Bronchiectasis in adult patients: an expression of heterozygosity for CFTR gene mutations?T Casals, J De-Gracia, M Gallego, et al.
Clinical Genetics|February 27, 2004
The influence of APOAV polymorphisms (T-1131>C and S19>W) on plasma triglyceride levels and risk of myocardial infarctionJ A Hubacek, Z Skodová, V Adámková, et al.
Clinical Genetics|February 27, 2004
The locus responsible for horizontal gaze palsy/progressive scoliosis and brainstem hypoplasia is refined to a 9-cM region on chromosome 11q23B Lo, M Faiyaz-Ul-Haque, B Banwell, et al.
Clinical Genetics|March 18, 2004
A new model for prediction of the age of onset and penetrance for Huntington's disease based on CAG lengthD R Langbehn, R R Brinkman, D Falush, et al.
Clinical Genetics|March 18, 2004
Mutational spectrum in Usher syndrome type IIX M Ouyang, D Yan, J F Hejtmancik, et al.
Clinical Genetics|March 18, 2004
The Mainz Severity Score Index: a new instrument for quantifying the Anderson-Fabry disease phenotype, and the response of patients to enzyme replacement therapyC Whybra, C Kampmann, F Krummenauer, et al.
Clinical Genetics|March 18, 2004
Current clinical selection strategies for identification of hereditary non-polyposis colorectal cancer families are inadequate: a meta-analysisW Kievit, J H F M de Bruin, E M M Adang, et al.
Clinical Genetics|March 18, 2004
Low frequency of myocilin mutations in Indian primary open-angle glaucoma patientsS Sripriya, S Uthra, R Sangeetha, et al.
Clinical Genetics|March 23, 2004
Screening for Down's syndrome in early and late first and second trimester using six maternal serum markersM Christiansen, S O Larsen, C Oxvig, et al.
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