Marles SL - Search Results

1

Long-term survival and normal cognitive development in infantile phosphofructokinase-1 deficiency.

Spriggs EL, Marles SL, Lacson A, McRae K, Bowman N, Sachdeva R, Monson R, Dilling L, Greenberg CR. Spriggs EL, et al. Among authors: marles sl. Clin Genet. 1999 Sep;56(3):235-7. doi: 10.1034/j.1399-0004.1999.560310.x. Clin Genet. 1999. PMID: 10563485 No abstract available.

2

Exclusion of the gelsolin gene on 9q32-34 as the cause of familial lattice corneal dystrophy type I.

Wiens A, Marles S, Safneck J, Kwiatkowski DJ, Maury CP, Zelinski T, Philipps S, Ekins MB, Greenberg CR. Wiens A, et al. Am J Hum Genet. 1992 Jul;51(1):156-60. Am J Hum Genet. 1992. PMID: 1319113 Free PMC article.

3

New familial syndrome of unilateral upper eyelid coloboma, aberrant anterior hairline pattern, and anal anomalies in Manitoba Indians.

Marles SL, Greenberg CR, Persaud TV, Shuckett EP, Chudley AE. Marles SL, et al. Am J Med Genet. 1992 Apr 1;42(6):793-9. doi: 10.1002/ajmg.1320420609. Am J Med Genet. 1992. PMID: 1554017

4

Evidence for Ritscher-Schinzel syndrome in Canadian Native Indians.

Marles SL, Chodirker BN, Greenberg CR, Chudley AE. Marles SL, et al. Am J Med Genet. 1995 May 8;56(4):343-50. doi: 10.1002/ajmg.1320560402. Am J Med Genet. 1995. PMID: 7604842 Review.

5

Identification of an uncommon haptoglobin type using DNA and protein analysis.

Marles SL, McAlpine PJ, Zelinski T, Phillips S, Maeda N, Greenberg CR. Marles SL, et al. Hum Genet. 1993 Oct;92(4):364-6. doi: 10.1007/BF01247336. Hum Genet. 1993. PMID: 8225317

6

Bowen-Conradi syndrome: a clinical and genetic study.

Lowry RB, Innes AM, Bernier FP, McLeod DR, Greenberg CR, Chudley AE, Chodirker B, Marles SL, Crumley MJ, Loredo-Osti JC, Morgan K, Fujiwara TM. Lowry RB, et al. Among authors: marles sl. Am J Med Genet A. 2003 Jul 30;120A(3):423-8. doi: 10.1002/ajmg.a.20059. Am J Med Genet A. 2003. PMID: 12838567

7

Manitoba Oculotrichoanal (MOTA) syndrome: report of eight new cases.

Li C, Marles SL, Greenberg CR, Chodirker BN, van de Kamp J, Slavotinek A, Chudley AE. Li C, et al. Among authors: marles sl. Am J Med Genet A. 2007 Apr 15;143A(8):853-7. doi: 10.1002/ajmg.a.31446. Am J Med Genet A. 2007. PMID: 17352387

8

Cytogenetic microarrays in Manitoba patients with developmental delay.

Dawson AJ, Riordan D, Tomiuk M, Konkin D, Anderson T, Bocangel P, Lwiwiski N, Saltel-Olson J, Marles S, Greenberg CR, Mhanni A, Chodirker BN, Chudley AE. Dawson AJ, et al. Clin Genet. 2009 May;75(5):498-500. doi: 10.1111/j.1399-0004.2009.01169.x. Clin Genet. 2009. PMID: 19475722 No abstract available.

9

Telemedicine diagnosis for fetal alcohol syndrome - The Manitoba experience.

Benoit T, Bowes C, Bowman N, Cantin D, Chudley A, Crolly D, Livingston A, Longstaffe S, Marles S, Miller C, Millar M, Penko M, Prasad C, Riguidel J, Wincott L. Benoit T, et al. Paediatr Child Health. 2002 Mar;7(3):147-51. doi: 10.1093/pch/7.3.147. Paediatr Child Health. 2002. PMID: 20046287 Free PMC article.

10

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. Among authors: marles sl. 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

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