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Author/Creator Ferguson, Marcia

1. GeneMatcher Aids in the Identification of a New Malformation Syndrome with Intellectual Disability, Unique Facial Dysmorphisms, and Skeletal and Connective Tissue Abnormalities Caused by De Novo Variants in HNRNPK. Issue 10 (6th August 2015)

Authors:
Au, P. Y. Billie; You, Jing; Caluseriu, Oana; Schwartzentruber, Jeremy; Majewski, Jacek; Bernier, Francois P.; Ferguson, Marcia; Valle, David; Parboosingh, Jillian S.; Sobreira, Nara; Innes, A. Micheil; Kline, Antonie D.
Journal:
Human mutation
Issue:
Volume 36:Issue 10(2015:Oct.)
Page Start:
1009
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. Poster abstracts. (1st September 2013)

Authors:
Wecht, Jill M.; Ivan, Adrian M.; Radulovic, Miroslav; Yen, Christina; Pena, Stephanie; Bauman, William A.; Ivan, Adrian M.; Radulovic, Miroslav; Rosado-Rivera, Dwindally; Yen, Christina; Bauman, William A.; Wecht, Jill M.; Flavin, Kara; Perkowski, Matthew; Poduri, Kanakadurga R.; Kirshblum, Steve...
Journal:
Journal of spinal cord medicine
Issue:
Volume 36:Number 5(2013:Sep.)
Page Start:
524
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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