Showing results 101 to 110 of 110
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Title | Author(s) | Issue Date | |
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1995 | |||
Severe intellectual disability and autistic features associated with microduplication 2q23.1 Journal:European Journal of Human Genetics | 2012 | ||
Sex specific methylation differences within the promoter of the non-coding RNA on the chromosome Xp11.4 suggest the maternal imprinted pattern Proceeding/Conference:Annual Meeting of the Organization for the study of Sex Differences, OSDD 2009 | 2009 | ||
Structure and chromosomal localization of the human constitutive endothelial nitric oxide synthase gene Journal:Journal of Biological Chemistry | 1993 | ||
1996 | |||
Translocation breakpoint maps 5 kb 3' from TWIST in a patient affected with Saethre-Chotzen syndrome Journal:Human Molecular Genetics | 1997 | ||
2017 | |||
Variation in the AU(AT)-rich element within the 3'-untranslated region of PPP1R3 is associated with variation in plasma glucose in aboriginal Canadians Journal:Journal of Clinical Endocrinology and Metabolism | 1998 | ||
1997 | |||
1995 |