Thomas MA - Search Results

1

Prenatal findings in 11 cases with craniofacial microsomia using the Alberta Congenital Anomalies Surveillance System, 1997-2019.

Thomas MA, Bedard T, Crawford S, Lowry RB. Thomas MA, et al. Am J Med Genet A. 2024 Aug;194(8):e63594. doi: 10.1002/ajmg.a.63594. Epub 2024 Mar 30. Am J Med Genet A. 2024. PMID: 38553895

2

Copy Number Variants and Congenital Anomalies Surveillance: A Suggested Coding Strategy Using the Royal College of Paediatrics and Child Health Version of ICD-10.

Bedard T, Lowry RB, Sibbald B, Thomas MA, Innes AM. Bedard T, et al. Among authors: thomas ma. J Registry Manag. 2016 Spring;43(1):6-9. J Registry Manag. 2016. PMID: 27195992

3

Prevalence rates study of selected isolated non-Mendelian congenital anomalies in the Hutterite population of Alberta, 1980-2016.

Lowry RB, Bedard T, Crawford S, Grevers X, Bernier FP, Thomas MA. Lowry RB, et al. Among authors: thomas ma. Am J Med Genet A. 2020 Nov;182(11):2594-2604. doi: 10.1002/ajmg.a.61834. Epub 2020 Sep 7. Am J Med Genet A. 2020. PMID: 32893972

4

Congenital hiatal hernia segregating with a duplication in 9q22.31q22.32 in two families.

Chang CA, Di Donato N, Hackmann K, Argiropoulos B, Ferreira P, Innes AM, Thomas MA. Chang CA, et al. Among authors: thomas ma. Am J Med Genet A. 2020 Dec;182(12):3040-3047. doi: 10.1002/ajmg.a.61898. Epub 2020 Oct 7. Am J Med Genet A. 2020. PMID: 33026187

5

The Alberta Congenital Anomalies Surveillance System: a 40-year review with prevalence and trends for selected congenital anomalies, 1997-2019.

Lowry RB, Bedard T, Grevers X, Crawford S, Greenway SC, Brindle ME, Sarnat HB, Harrop AR, Kiefer GN, Thomas MA. Lowry RB, et al. Among authors: thomas ma. Health Promot Chronic Dis Prev Can. 2023 Jan;43(1):40-48. doi: 10.24095/hpcdp.43.1.04. Health Promot Chronic Dis Prev Can. 2023. PMID: 36651885 Free PMC article.

6

Craniofacial Microsomia, Associated Congenital Anomalies, and Risk Factors in 63 Cases from the Alberta Congenital Anomalies Surveillance System.

Thomas MA, Bedard T, Crawford S, Grevers X, Lowry RB. Thomas MA, et al. J Pediatr. 2023 Oct;261:113528. doi: 10.1016/j.jpeds.2023.113528. Epub 2023 Jun 1. J Pediatr. 2023. PMID: 37268037

7

Review of the recurrent 8q13.2q13.3 branchio-oto-renal related microdeletion, and report of an additional case with associated distal arthrogryposis.

Au PB, Chernos JE, Thomas MA. Au PB, et al. Among authors: thomas ma. Am J Med Genet A. 2016 Nov;170(11):2984-2987. doi: 10.1002/ajmg.a.37695. Epub 2016 Aug 19. Am J Med Genet A. 2016. PMID: 27542115 Review.

8

Canadian College of Medical Geneticists: clinical practice advisory document - responsibility to recontact for reinterpretation of clinical genetic testing.

Goh ES, Chad L, Richer J, Bombard Y, Mighton C, Agatep R, Lacaria M, Penny B, Thomas MA, Zawati MH, MacFarlane J, Laberge AM, Nelson TN. Goh ES, et al. Among authors: thomas ma. J Med Genet. 2024 Nov 25;61(12):1123-1131. doi: 10.1136/jmg-2024-110330. J Med Genet. 2024. PMID: 39362754 Free PMC article.

9

Prenatal diagnosis of monosomy 1p36: a focus on brain abnormalities and a review of the literature.

Campeau PM, Ah Mew N, Cartier L, Mackay KL, Shaffer LG, Der Kaloustian VM, Thomas MA. Campeau PM, et al. Among authors: thomas ma. Am J Med Genet A. 2008 Dec 1;146A(23):3062-9. doi: 10.1002/ajmg.a.32563. Am J Med Genet A. 2008. PMID: 19006213 Review.

10

9p13.1p13.3 interstitial deletion: A case report and further delineation of a rare condition.

Crone M, Thomas MA. Crone M, et al. Among authors: thomas ma. Am J Med Genet A. 2016 Apr;170A(4):1095-8. doi: 10.1002/ajmg.a.37534. Epub 2016 Jan 5. Am J Med Genet A. 2016. PMID: 26728902 No abstract available.

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