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Howard R Slater

Showing results (41-50 of 43) with videos related to

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Molecular Autism|May 11, 2019
Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic featuresEmma K Baker, Marta Arpone, Solange M Aliaga, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 28, 2013
Molecular and clinical characterization of 25 individuals with exonic deletions of NRXN1 and comprehensive review of the literatureFrédérique Béna, Damien L Bruno, Mats Eriksson, et al.
Journal of Medical Genetics|May 11, 2010
Further molecular and clinical delineation of co-locating 17p13.3 microdeletions and microduplications that show distinctive phenotypesDamien L Bruno, Britt-Marie Anderlid, Anna Lindstrand, et al.
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Showing results (41-50 of 43) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 43 results.
Molecular Autism|May 11, 2019
Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic featuresEmma K Baker, Marta Arpone, Solange M Aliaga, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 28, 2013
Molecular and clinical characterization of 25 individuals with exonic deletions of NRXN1 and comprehensive review of the literatureFrédérique Béna, Damien L Bruno, Mats Eriksson, et al.
Journal of Medical Genetics|May 11, 2010
Further molecular and clinical delineation of co-locating 17p13.3 microdeletions and microduplications that show distinctive phenotypesDamien L Bruno, Britt-Marie Anderlid, Anna Lindstrand, et al.
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