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Clinical Genetics|September 10, 2004
T-box genes and congenital heart/limb malformationsD Isphording, A M Leylek, J Yeung, et al.
Clinical Genetics|September 10, 2004
Genetic variation at the perilipin (PLIN) locus is associated with obesity-related phenotypes in White womenL Qi, D Corella, J V Sorlí, et al.
Clinical Genetics|September 10, 2004
Genetic discrimination: the clinician perspectiveR Nedelcu, K R Blazer, B U Schwerin, et al.
Clinical Genetics|August 25, 2004
Family cancer histories predictive of a high risk of hereditary non-polyposis colorectal cancer associate significantly with a genomic rearrangement in hMSH2 or hMLH1P J Ainsworth, D Koscinski, B P Fraser, et al.
Clinical Genetics|August 25, 2004
A previously undescribed frameshift deletion mutation of HFE (c.del277; G93fs) associated with hemochromatosis and iron overload in a C282Y heterozygoteJ C Barton, C West, P L Lee, et al.
Clinical Genetics|August 25, 2004
Cholesteryl ester transfer protein promoter single-nucleotide polymorphisms in Sp1-binding sites affect transcription and are associated with high-density lipoprotein cholesterolJ F Thompson, D B Lloyd, M E Lira, et al.
Clinical Genetics|September 1, 1978
Prevalence of thyroid disorder in Down syndromeZ Sare, R H Ruvalcaba, V C Kelley
Clinical Genetics|September 1, 1978
A "new" autosomal dominant genodermatosis characterized by hyperpigmented spots and plamoplantar hyperkeratosisJ M Cantú, J Sánchez-Corona, R Fragoso, et al.
Clinical Genetics|July 1, 1992
Elevated serum levels of creatine kinase BB in autosomal dominant osteopetrosis type II--a family studyT Yoneyama, H L Fowler, J W Pendleton, et al.
Clinical Genetics|November 1, 1992
Fertility in myotonic dystrophy in Saguenay-Lac-St-Jean: a historical perspectiveT N Dao, J Mathieu, J P Bouchard, et al.
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