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Human Genetics|April 21, 2005
A newly identified RET proto-oncogene polymorphism is found in a high number of endocrine tumor patientsWolfgang Gartner, Ivelina Mineva, Teodora Daneva, et al.Human Genetics|April 1, 1992
Alport syndrome caused by a 5' deletion within the COL4A5 geneA Renieri, M Seri, J C Myers, et al.Human Genetics|April 1, 1992
Chromosome-band-specific painting: chromosome in situ suppression hybridization using PCR products from a microdissected chromosome band as a probe poolH X Deng, K Yoshiura, R W Dirks, et al.Human Genetics|April 1, 1992
Molecular cytogenetic analysis of XX males using Y-specific DNA sequences, including SRYB Van der Auwera, N Van Roy, A De Paepe, et al.Human Genetics|April 1, 1992
Abnormal lymphokine production: a novel feature of the genetic disease Fanconi anemia. I. Involvement of interleukin-6F Rosselli, J Sanceau, J Wietzerbin, et al.Human Genetics|April 1, 1992
Detection of small RB1 gene deletions in retinoblastoma by multiplex PCR and high-resolution gel electrophoresisD Lohmann, B Horsthemke, G Gillessen-Kaesbach, et al.Human Genetics|April 1, 1992
Confirmation of linkage of benign familial neonatal convulsions to D20S19 and D20S20A Malafosse, M Leboyer, O Dulac, et al.Human Genetics|April 1, 1992
The French Canadian Tay-Sachs disease deletion mutation: identification of probable foundersM De Braekeleer, P Hechtman, E Andermann, et al.Human Genetics|April 1, 1992
Beta S haplotypes in various world populationsC Oner, A J Dimovski, N F Olivieri, et al.Human Genetics|October 7, 2005
Systemic lupus erythematosus susceptibility loci defined by genome scan meta-analysisYoung Ho Lee, Swapan K NathPageof 957