Morgan K - Search Results

1

Prevalence of carriers of premutation-size alleles of the FMRI gene--and implications for the population genetics of the fragile X syndrome.

Rousseau F, Rouillard P, Morel ML, Khandjian EW, Morgan K. Rousseau F, et al. Among authors: morgan k. Am J Hum Genet. 1995 Nov;57(5):1006-18. Am J Hum Genet. 1995. PMID: 7485149 Free PMC article.

2

Premutation and intermediate-size FMR1 alleles in 10572 males from the general population: loss of an AGG interruption is a late event in the generation of fragile X syndrome alleles.

Dombrowski C, Lévesque S, Morel ML, Rouillard P, Morgan K, Rousseau F. Dombrowski C, et al. Among authors: morgan k. Hum Mol Genet. 2002 Feb 15;11(4):371-8. doi: 10.1093/hmg/11.4.371. Hum Mol Genet. 2002. PMID: 11854169

3

Screening and instability of FMR1 alleles in a prospective sample of 24,449 mother-newborn pairs from the general population.

Lévesque S, Dombrowski C, Morel ML, Rehel R, Côté JS, Bussières J, Morgan K, Rousseau F. Lévesque S, et al. Among authors: morgan k. Clin Genet. 2009 Dec;76(6):511-23. doi: 10.1111/j.1399-0004.2009.01237.x. Epub 2009 Oct 23. Clin Genet. 2009. PMID: 19863547

4

The association between heel ultrasound and hormone replacement therapy is modulated by a two-locus vitamin D and estrogen receptor genotype.

Giguère Y, Dodin S, Blanchet C, Morgan K, Rousseau F. Giguère Y, et al. Among authors: morgan k. J Bone Miner Res. 2000 Jun;15(6):1076-84. doi: 10.1359/jbmr.2000.15.6.1076. J Bone Miner Res. 2000. PMID: 10841176 Free article.

5

Beta-thalassemia genes in French-Canadians: haplotype and mutation analysis of Portneuf chromosomes.

Kaplan F, Kokotsis G, DeBraekeleer M, Morgan K, Scriver CR. Kaplan F, et al. Among authors: morgan k. Am J Hum Genet. 1990 Jan;46(1):126-32. Am J Hum Genet. 1990. PMID: 1967205 Free PMC article.

6

Identification of deletion and triple alpha-globin gene haplotypes in the Montreal beta-thalassemia screening program: implications for genetic medicine.

Akerman BR, Fujiwara TM, Lancaster GA, Morgan K, Scriver CR. Akerman BR, et al. Among authors: morgan k. Am J Med Genet. 1990 May;36(1):76-84. doi: 10.1002/ajmg.1320360115. Am J Med Genet. 1990. PMID: 2333910

7

Linkage disequilibrium analysis of childhood-onset spinal muscular atrophy (SMA) in the French-Canadian population.

Simard LR, Prescott G, Rochette C, Morgan K, Lemieux B, Mathieu J, Melançon SB, Vanasse M. Simard LR, et al. Among authors: morgan k. Hum Mol Genet. 1994 Mar;3(3):459-63. doi: 10.1093/hmg/3.3.459. Hum Mol Genet. 1994. PMID: 8012358

8

Location score and haplotype analyses of the locus for autosomal recessive spastic ataxia of Charlevoix-Saguenay, in chromosome region 13q11.

Richter A, Rioux JD, Bouchard JP, Mercier J, Mathieu J, Ge B, Poirier J, Julien D, Gyapay G, Weissenbach J, Hudson TJ, Melançon SB, Morgan K. Richter A, et al. Among authors: morgan k. Am J Hum Genet. 1999 Mar;64(3):768-75. doi: 10.1086/302274. Am J Hum Genet. 1999. PMID: 10053011 Free PMC article.

9

Localization of a recessive gene for North American Indian childhood cirrhosis to chromosome region 16q22-and identification of a shared haplotype.

Bétard C, Rasquin-Weber A, Brewer C, Drouin E, Clark S, Verner A, Darmond-Zwaig C, Fortin J, Mercier J, Chagnon P, Fujiwara TM, Morgan K, Richter A, Hudson TJ, Mitchell GA. Bétard C, et al. Among authors: morgan k. Am J Hum Genet. 2000 Jul;67(1):222-8. doi: 10.1086/302993. Epub 2000 May 11. Am J Hum Genet. 2000. PMID: 10820129 Free PMC article.

10

A frequent regulatory variant of the estrogen-related receptor alpha gene associated with BMD in French-Canadian premenopausal women.

Laflamme N, Giroux S, Loredo-Osti JC, Elfassihi L, Dodin S, Blanchet C, Morgan K, Giguère V, Rousseau F. Laflamme N, et al. Among authors: morgan k. J Bone Miner Res. 2005 Jun;20(6):938-44. doi: 10.1359/JBMR.050203. Epub 2005 Feb 7. J Bone Miner Res. 2005. PMID: 15883633 Free article.

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