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Nature Genetics|August 1, 1995
Different chromosomal localization of the Clcn4 gene in Mus spretus and C57BL/6J miceE I Rugarli, D A Adler, G Borsani, et al.Proceedings of the National Academy of Sciences of the United States of America|July 1, 1987
Isolation and characterization of a steroid sulfatase cDNA clone: genomic deletions in patients with X-chromosome-linked ichthyosisA Ballabio, G Parenti, R Carrozzo, et al.Nature Genetics|December 1, 1992
Kallmann syndrome gene on the X and Y chromosomes: implications for evolutionary divergence of human sex chromosomesB Incerti, S Guioli, A Pragliola, et al.American Journal of Medical Genetics|December 31, 1997
X-linked recessive chondrodysplasia punctata due to a new point mutation of the ARSE geneG Parenti, P Buttitta, G Meroni, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 1, 2008
No association with the 5,10-methylenetetrahydrofolate reductase gene and major depressive disorder: results of the depression case control (DeCC) study and a meta-analysisD Gaysina, S Cohen, N Craddock, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 25, 2005
Association analysis of monoamine genes with measures of depression and anxiety in a selected community sample of siblingsM W Nash, K Sugden, P Huezo-Diaz, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|May 20, 1982
Platelet monoamine oxidase: specific activity and turnover number in headacheK M Summers, G K Brown, I W Craig, et al.Human Molecular Genetics|December 15, 2000
Allele association studies with SSR and SNP markers at known physical distances within a 1 Mb region embracing the ALDH2 locus in the Japanese, demonstrates linkage disequilibrium extending up to 400 kbH G Koch, J McClay, E W Loh, et al.Human Molecular Genetics|July 13, 1999
MID2, a homologue of the Opitz syndrome gene MID1: similarities in subcellular localization and differences in expression during developmentG Buchner, E Montini, G Andolfi, et al.Annales De Chirurgie|January 1, 1992
[Non-malignant esophagotracheal fistulas in adults. Experience with 35 cases]R Giudicelli, J M Sainty, A Barthélémy, et al.Pageof 30