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Author/Creator Hume, Stacey

1. Assessing the cost of implementing the 2011 Society of Obstetricians and Gynecologists of Canada and Canadian College of Medical Genetics practice guidelines on the detection of fetal aneuploidies. (7th August 2017)

Authors:
Lilley, Margaret; Hume, Stacey; Karpoff, Nina; Maire, Georges; Taylor, Sherry; Tomaszewski, Robert; Yoshimoto, Maisa; Christian, Susan
Journal:
Prenatal diagnosis
Issue:
Volume 37:Number 9(2017)
Page Start:
916
Record Type:
Journal Article
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2. CCMG practice guideline: laboratory guidelines for next-generation sequencing. Issue 12 (12th July 2019)

Authors:
Hume, Stacey; Nelson, Tanya N; Speevak, Marsha; McCready, Elizabeth; Agatep, Ron; Feilotter, Harriet; Parboosingh, Jillian; Stavropoulos, Dimitri J; Taylor, Sherryl; Stockley, Tracy L
Journal:
Journal of medical genetics
Issue:
Volume 56:Issue 12(2019)
Page Start:
792
Record Type:
Journal Article
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4. Data sharing to improve concordance in variant interpretation across laboratories: results from the Canadian Open Genetics Repository. Issue 6 (19th April 2021)

Authors:
Mighton, Chloe; Smith, Amanda C; Mayers, Justin; Tomaszewski, Robert; Taylor, Sherryl; Hume, Stacey; Agatep, Ron; Spriggs, Elizabeth; Feilotter, Harriet E; Semenuk, Laura; Wong, Henry; Lazo de la Vega, Lorena; Marshall, Christian R; Axford, Michelle M; Silver, Talia; Charames, George S; Di Gioacc...
Other Names:
author non-byline.; Agatep Ron author non-byline.; Ainsworth Peter author non-byline.; Akbari Mohammad R. author non-byline.; Aronson Melyssa author non-byline.; Basran Raveen author non-byline.; Blavier Andre author non-byline.; Blumenthal Andrea author non-byline.; Bombard Yvonne author non-by...
Journal:
Journal of medical genetics
Issue:
Volume 59:Issue 6(2022)
Page Start:
571
Record Type:
Journal Article
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6. The clinical application of genome-wide sequencing for monogenic diseases in Canada: Position Statement of the Canadian College of Medical Geneticists. Issue 7 (7th May 2015)

Authors:
Boycott, Kym; Hartley, Taila; Adam, Shelin; Bernier, Francois; Chong, Karen; Fernandez, Bridget A; Friedman, Jan M; Geraghty, Michael T; Hume, Stacey; Knoppers, Bartha M; Laberge, Anne-Marie; Majewski, Jacek; Mendoza-Londono, Roberto; Meyn, M Stephen; Michaud, Jacques L; Nelson, Tanya N; Richer, ...
Journal:
Journal of medical genetics
Issue:
Volume 52:Issue 7(2015)
Page Start:
431
Record Type:
Journal Article
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7. The novel p.Ser263Phe mutation in the human high‐affinity choline transporter 1 (CHT1/SLC5A7) causes a lethal form of fetal akinesia syndrome. Issue 10 (12th July 2019)

Authors:
Banerjee, Mayukh; Arutyunov, Denis; Brandwein, Daniel; Janetzki‐Flatt, Cassandra; Kolski, Hanna; Hume, Stacey; Leonard, Norma Jean; Watt, James; Lacson, Atilano; Baradi, Monica; Leslie, Elaine M.; Cordat, Emmanuelle; Caluseriu, Oana
Journal:
Human mutation
Issue:
Volume 40:Issue 10(2019)
Page Start:
1676
Record Type:
Journal Article
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