Development of a diagnostic DNA chip to screen for 30 autosomal recessive disorders in the Hutterite population-Reference-Cited by-同舟云学术

Development of a diagnostic DNA chip to screen for 30 autosomal recessive disorders in the Hutterite population

Published:2016-01-19 Issue:3 Volume:4 Page:312-321
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Triggs‐Raine Barbara¹²³^ORCID,Dyck Tamara⁴,Boycott Kym M.⁵,Innes A. Micheil⁶,Ober Carole⁷,Parboosingh Jillian S.⁶,Botkin Alexis²,Greenberg Cheryl R.¹²³,Spriggs Elizabeth L.¹²⁴

Affiliation:

1. Departments of Biochemistry & Medical Genetics University of Manitoba Winnipeg Canada

2. Pediatrics & Child Health University of Manitoba 745 Bannatyne Ave. Winnipeg MB R3E 0J9 Canada

3. The Manitoba Institute of Child Health 513‐715 McDermot Ave. Winnipeg MB R3E 3P4 Canada

4. Clinical Biochemistry and Genetics Diagnostic Services Manitoba at Health Sciences Centre Winnipeg MB R3A 1R9 Canada

5. Children's Hospital of Eastern Ontario Research Institute University of Ottawa Ottawa ON K1H 8L1 Canada

6. Department of Medical Genetics Alberta Children's Hospital and Alberta Children's Hospital Research Institute for Child and Maternal Health Cumming School of Medicine University of Calgary Calgary Alberta Canada

7. Departments of Human Genetics and Obstetrics and Gynecology The University of Chicago Chicago Illinois

Funder

Diagnostic Services Manitoba

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.206

Reference42 articles.

1. Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F

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3. Recessive TRAPPC11 Mutations Cause a Disease Spectrum of Limb Girdle Muscular Dystrophy and Myopathy with Movement Disorder and Intellectual Disability

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