Clinical and genetic heterogeneity in Dubowitz syndrome: Implications for diagnosis, management and further research-Reference-Cited by-同舟云学术

Clinical and genetic heterogeneity in Dubowitz syndrome: Implications for diagnosis, management and further research

Published:2018-12 Issue:4 Volume:178 Page:387-397
ISSN:1552-4868
Container-title:American Journal of Medical Genetics Part C: Seminars in Medical Genetics
language:en
Short-container-title:Am J Med Genet

Author:

Innes A. Micheil¹²^ORCID,McInnes Brenda L.¹,Dyment David A.³⁴^ORCID

Affiliation:

1. Department of Medical Genetics; University of Calgary; Calgary Alberta Canada

2. Alberta Children's Hospital Research Institute; University of Calgary; Calgary Alberta Canada

3. Department of Genetics; Children's Hospital of Eastern Ontario; Ottawa Ontario Canada

4. Children's Hospital of Eastern Ontario Research Institute; Ottawa Ontario Canada

Funder

Children's Hospital of Eastern Ontario Foundation

Genome Quebec

Genome British Columbia

Genome Alberta

Ontario Research Fund

Canadian Institutes of Health Research

Ontario Genomics Institute

Genome Canada

National Organization for Rare Disorders

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

Reference72 articles.

5. Primordial dwarfism: An update;Alkuraya;Current Opinion in Endocrinology, Diabetes, and Obesity,2015

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