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Patricia Heard

Showing results (11-20 of 16) with videos related to

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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|August 4, 2015
Consequences of chromsome18q deletionsJannine D Cody, Courtney Sebold, Patricia Heard, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|August 8, 2015
A review of 18p deletionsMinire Hasi-Zogaj, Courtney Sebold, Patricia Heard, et al.
American Journal of Medical Genetics. Part A|May 9, 2007
Recurrent interstitial deletions of proximal 18q: a new syndrome involving expressive speech delayJannine D Cody, Courtney Sebold, Amtul Malik, et al.
American Journal of Medical Genetics. Part A|August 31, 2010
Tetrasomy 18p: report of the molecular and clinical findings of 43 individualsCourtney Sebold, Elizabeth Roeder, Marsha Zimmerman, et al.
Human Mutation|March 31, 2015
Hemizygosity for SMCHD1 in Facioscapulohumeral Muscular Dystrophy Type 2: Consequences for 18p Deletion SyndromeRichard J L F Lemmers, Marlinde L van den Boogaard, Patrick J van der Vliet, et al.
Journal of Medical Genetics|March 23, 2018
Monosomy 18p is a risk factor for facioscapulohumeral dystrophyJudit Balog, Remko Goossens, Richard J L F Lemmers, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|August 4, 2015
Consequences of chromsome18q deletionsJannine D Cody, Courtney Sebold, Patricia Heard, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|August 8, 2015
A review of 18p deletionsMinire Hasi-Zogaj, Courtney Sebold, Patricia Heard, et al.
American Journal of Medical Genetics. Part A|May 9, 2007
Recurrent interstitial deletions of proximal 18q: a new syndrome involving expressive speech delayJannine D Cody, Courtney Sebold, Amtul Malik, et al.
American Journal of Medical Genetics. Part A|August 31, 2010
Tetrasomy 18p: report of the molecular and clinical findings of 43 individualsCourtney Sebold, Elizabeth Roeder, Marsha Zimmerman, et al.
Human Mutation|March 31, 2015
Hemizygosity for SMCHD1 in Facioscapulohumeral Muscular Dystrophy Type 2: Consequences for 18p Deletion SyndromeRichard J L F Lemmers, Marlinde L van den Boogaard, Patrick J van der Vliet, et al.
Journal of Medical Genetics|March 23, 2018
Monosomy 18p is a risk factor for facioscapulohumeral dystrophyJudit Balog, Remko Goossens, Richard J L F Lemmers, et al.
Pageof 2