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Author/Creator Morel, Chantal F.

1. A case of secondary acute myeloid leukemia on a background of glycogen storage disease with chronic neutropenia treated with granulocyte colony stimulating factor. Issue 1 (23rd July 2019)

Authors:
Khalaf, Dina; Bell, Heather; Dale, David; Gupta, Vikas; Faghfoury, Hanna; Morel, Chantal F.; Tierens, Anne; Weinstein, David A.; Yan, Jiong; Thyagu, Santhosh; Maze, Dawn
Journal:
JIMD reports
Issue:
Volume 49:Issue 1(2019)
Page Start:
37
Record Type:
Journal Article
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2. Clinical Significance of Papillary Muscles on Left Ventricular Mass Quantification Using Cardiac Magnetic Resonance Imaging: Reproducibility and Prognostic Value in Fabry Disease. Issue 4 (July 2021)

Authors:
Al-Arnawoot, Amna; O'Brien, Ciara; Karur, Gauri R.; Nguyen, Elsie T.; Wasim, Syed; Iwanochko, Robert M.; Morel, Chantal F.; Hanneman, Kate
Journal:
Journal of thoracic imaging
Issue:
Volume 36:Issue 4(2021)
Page Start:
Record Type:
Journal Article
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4. Mandibulofacial Dysostosis with Microcephaly: Mutation and Database Update. Issue 2 (19th November 2015)

Authors:
Huang, Lijia; Vanstone, Megan R.; Hartley, Taila; Osmond, Matthew; Barrowman, Nick; Allanson, Judith; Baker, Laura; Dabir, Tabib A.; Dipple, Katrina M.; Dobyns, William B.; Estrella, Jane; Faghfoury, Hanna; Favaro, Francine P.; Goel, Himanshu; Gregersen, Pernille A.; Gripp, Karen W.; Grix, Art; G...
Journal:
Human mutation
Issue:
Volume 37:Issue 2(2016)
Page Start:
148
Record Type:
Journal Article
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5. Novel folliculin gene mutation and an elevated serum vascular endothelial growth factor-D level in the context of cystic lung disease. Issue 1 (24th February 2022)

Authors:
Hambly, Nathan; Bhalla, Anurag; Lorello, Gianni R.; Morel, Chantal F.; Hoffstein, Victor
Journal:
Canadian journal of respiratory, critical care, and sleep medicine =
Issue:
Volume 6:Issue 1(2022)
Page Start:
58
Record Type:
Journal Article
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6. Reappraisal of Reported Genes for Sudden Arrhythmic Death: Evidence-Based Evaluation of Gene Validity for Brugada Syndrome. Issue 12 (18th September 2018)

Authors:
Hosseini, S. Mohsen; Kim, Raymond; Udupa, Sharmila; Costain, Gregory; Jobling, Rebekah; Liston, Eriskay; Jamal, Seema M.; Szybowska, Marta; Morel, Chantal F.; Bowdin, Sarah; Garcia, John; Care, Melanie; Sturm, Amy C.; Novelli, Valeria; Ackerman, Michael J.; Ware, James S.; Hershberger, Ray E.; Wi...
Journal:
Circulation
Issue:
Volume 138:Issue 12(2018)
Page Start:
Record Type:
Journal Article
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7. Whole exome sequencing identified 1 base pair novel deletion in BCL2‐associated athanogene 3 (BAG3) gene associated with severe dilated cardiomyopathy (DCM) requiring heart transplant in multiple family members. Issue 3 (March 2017)

Authors:
Rafiq, Muhammad Arshad; Chaudhry, Ayeshah; Care, Melanie; Spears, Danna A.; Morel, Chantal F.; Hamilton, Robert M.
Journal:
American journal of medical genetics
Issue:
Volume 173:Issue 3(2017)
Page Start:
699
Record Type:
Journal Article
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8. Whole exome sequencing identified 1 base pair novel deletion in BCL2‐associated athanogene 3 (BAG3) gene associated with severe dilated cardiomyopathy (DCM) requiring heart transplant in multiple family members. Issue 3 (17th February 2017)

Authors:
Rafiq, Muhammad Arshad; Chaudhry, Ayeshah; Care, Melanie; Spears, Danna A.; Morel, Chantal F.; Hamilton, Robert M.
Journal:
American journal of medical genetics
Issue:
Volume 173:Issue 3(2017)
Page Start:
699
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗