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Human Immunology|May 16, 2006
Disease relevant HLA class II alleles isolated by genotypic, haplotypic, and sequence analysis in North American Caucasians with pemphigus vulgarisErica Lee, Katherine A Lendas, Selwyn Chow, et al.Journal of Plastic, Reconstructive & Aesthetic Surgery : JPRAS|May 4, 2023
A UK consensus statement on thromboprophylaxis for autologous breast reconstructionJessica A Savage, Beverley J Hunt, Gerard Stansby, et al.Genomics|August 12, 2008
Genome-wide linkage analysis of an autosomal recessive hypotrichosis identifies a novel P2RY5 mutationLynn Petukhova, Edilson C Sousa, Amalia Martinez-Mir, et al.Pediatric Research|February 1, 2012
IL-18R1 and IL-18RAP SNPs may be associated with bronchopulmonary dysplasia in African-American infantsJoanna Floros, Douglas Londono, Derek Gordon, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 14, 2008
Catechol-O-methyltransferase (COMT) gene variants: possible association of the Val158Met variant with opiate addiction in Hispanic womenBronson E Oosterhuis, K Steven LaForge, Dmitri Proudnikov, et al.The Journal of Investigative Dermatology|November 25, 2003
Germline fumarate hydratase mutations in families with multiple cutaneous and uterine leiomyomataAmalia Martinez-Mir, Benjamin Glaser, Gary S Chuang, et al.BMC Proceedings|December 19, 2009
Growth mixture modeling as an exploratory analysis tool in longitudinal quantitative trait loci analysisSu-Wei Chang, Seung Hoan Choi, Ke Li, et al.Genetic Epidemiology|October 6, 2005
Localization of breast cancer susceptibility loci by genome-wide SNP linkage disequilibrium mappingNathan A Ellis, Tomas Kirchhoff, Nandita Mitra, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 29, 2015
Deficits in Trabecular Bone Microarchitecture in Young Women With Type 1 Diabetes MellitusNaiemh Abdalrahaman, Christie McComb, John E Foster, et al.American Journal of Human Genetics|April 17, 2007
CHD7 gene polymorphisms are associated with susceptibility to idiopathic scoliosisXiaochong Gao, Derek Gordon, Dongping Zhang, et al.Pageof 10