Elliott AM - Search Results

1

Trends in telehealth versus on-site clinical genetics appointments in Manitoba: a comparative study.

Elliott AM, Mhanni AA, Marles SL, Greenberg CR, Chudley AE, Nyhof GC, Chodirker BN. Elliott AM, et al. J Genet Couns. 2012 Apr;21(2):337-44. doi: 10.1007/s10897-011-9406-5. Epub 2011 Oct 15. J Genet Couns. 2012. PMID: 21997346

2

Evaluation of a clinical genetics service--a quality initiative.

Elliott AM, Chodirker BN, Bocangel P, Mhanni AA. Elliott AM, et al. J Genet Couns. 2014 Oct;23(5):881-9. doi: 10.1007/s10897-014-9713-8. Epub 2014 Mar 21. J Genet Couns. 2014. PMID: 24647747

3

Clinical and epidemiological findings in patients with central ray deficiency: split hand foot malformation (SHFM) in Manitoba, Canada.

Elliott AM, Reed MH, Chudley AE, Chodirker BN, Evans JA. Elliott AM, et al. Am J Med Genet A. 2006 Jul 1;140(13):1428-39. doi: 10.1002/ajmg.a.31245. Am J Med Genet A. 2006. PMID: 16673359

4

A novel mutation in KIAA0196: identification of a gene involved in Ritscher-Schinzel/3C syndrome in a First Nations cohort.

Elliott AM, Simard LR, Coghlan G, Chudley AE, Chodirker BN, Greenberg CR, Burch T, Ly V, Hatch GM, Zelinski T. Elliott AM, et al. J Med Genet. 2013 Dec;50(12):819-22. doi: 10.1136/jmedgenet-2013-101715. Epub 2013 Sep 24. J Med Genet. 2013. PMID: 24065355

5

Radiographic characterization of the hands in Ritscher-Schinzel/3-C syndrome.

Friesen KJ, Chodirker BN, Chudley AE, Reed MH, Elliott AM. Friesen KJ, et al. Among authors: elliott am. Springerplus. 2013 Nov 7;2:594. doi: 10.1186/2193-1801-2-594. eCollection 2013. Springerplus. 2013. PMID: 24255872 Free PMC article.

6

Split hand foot malformation (SHFM).

Elliott AM, Evans JA, Chudley AE. Elliott AM, et al. Clin Genet. 2005 Dec;68(6):501-5. doi: 10.1111/j.1399-0004.2005.00530.x. Clin Genet. 2005. PMID: 16283879 Review.

7

A novel COMP mutation in an Inuit patient with pseudoachondroplasia and severe short stature.

Elliott AM, Bocangel P, Reed MH, Greenberg CR. Elliott AM, et al. Genet Mol Res. 2010 Sep 8;9(3):1785-90. doi: 10.4238/vol9-3gmr897. Genet Mol Res. 2010. PMID: 20830670 Free article.

8

Potential teratogenic effects of allopurinol: a case report.

Kozenko M, Grynspan D, Oluyomi-Obi T, Sitar D, Elliott AM, Chodirker BN. Kozenko M, et al. Among authors: elliott am. Am J Med Genet A. 2011 Sep;155A(9):2247-52. doi: 10.1002/ajmg.a.34139. Epub 2011 Aug 3. Am J Med Genet A. 2011. PMID: 21815259

9

The duplicated longitudinal epiphysis or "kissing delta phalanx": evolution and variation in three different disorders.

Elliott AM, Evans JA, Chudley AE, Reed MH. Elliott AM, et al. Skeletal Radiol. 2004 Jun;33(6):345-51. doi: 10.1007/s00256-004-0752-3. Epub 2004 May 6. Skeletal Radiol. 2004. PMID: 15138725

10

Cenani-Lenz syndactyly in a patient with features of Kabuki syndrome.

Elliott AM, Reed MH, Evans JA, Cross HG, Chudley AE. Elliott AM, et al. Clin Dysmorphol. 2004 Jul;13(3):143-150. doi: 10.1097/01.mcd.0000127466.26888.15. Clin Dysmorphol. 2004. PMID: 15194949

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