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American Journal of Medical Genetics. Part A
|
September 26, 2008
Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi (CLOVE) syndrome: CNS malformations and seizures may be a component of this disorder
Zoran S Gucev, Velibor Tasic, Aleksandra Jancevska, et al.
NPJ Genomic Medicine
|
December 22, 2017
Genomic medicine in the military
Mauricio De Castro, Leslie G Biesecker, Clesson Turner, et al.
Cognition & Emotion
|
December 9, 2014
The role of current affect, anticipated affect and spontaneous self-affirmation in decisions to receive self-threatening genetic risk information
Rebecca A Ferrer, Jennifer M Taber, William M P Klein, et al.
Circulation. Genomic and Precision Medicine
|
June 1, 2018
Ability of Patients to Distinguish Among Cardiac Genomic Variant Subclassifications
Lydia D Hellwig, Barbara B Biesecker, Katie L Lewis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 4, 2017
Reactions to clinical reinterpretation of a gene variant by participants in a sequencing study
Jennifer M Taber, William M P Klein, Katie L Lewis, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
September 7, 2019
Thrombosis risk factors in PIK3CA-related overgrowth spectrum and Proteus syndrome
Kim M Keppler-Noreuil, Jay Lozier, Neal Oden, et al.
Nature Genetics
|
May 10, 2000
Mutation of a gene encoding a putative chaperonin causes McKusick-Kaufman syndrome
D L Stone, A Slavotinek, G G Bouffard, et al.
BMC Medical Genetics
|
July 29, 2011
Brain tissue- and region-specific abnormalities on volumetric MRI scans in 21 patients with Bardet-Biedl syndrome (BBS)
Kim M Keppler-Noreuil, Catherine Blumhorst, Julie C Sapp, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 16, 2010
Recurrence risks for Bardet-Biedl syndrome: Implications of locus heterogeneity
Julie C Sapp, Darryl Nishimura, Jennifer J Johnston, et al.
American Journal of Medical Genetics. Part A
|
May 19, 2009
Molecular characterization of co-occurring Duchenne muscular dystrophy and X-linked oculo-facio-cardio-dental syndrome in a girl
Yong-hui Jiang, Ping Fang, Adekunle M Adesina, et al.
Page
of 48
Search research articles
Search
Showing results (231-240 of 475) with videos related to
Sort By:
Page
of 48
American Journal of Medical Genetics. Part A
|
September 26, 2008
Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi (CLOVE) syndrome: CNS malformations and seizures may be a component of this disorder
Zoran S Gucev, Velibor Tasic, Aleksandra Jancevska, et al.
NPJ Genomic Medicine
|
December 22, 2017
Genomic medicine in the military
Mauricio De Castro, Leslie G Biesecker, Clesson Turner, et al.
Cognition & Emotion
|
December 9, 2014
The role of current affect, anticipated affect and spontaneous self-affirmation in decisions to receive self-threatening genetic risk information
Rebecca A Ferrer, Jennifer M Taber, William M P Klein, et al.
Circulation. Genomic and Precision Medicine
|
June 1, 2018
Ability of Patients to Distinguish Among Cardiac Genomic Variant Subclassifications
Lydia D Hellwig, Barbara B Biesecker, Katie L Lewis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 4, 2017
Reactions to clinical reinterpretation of a gene variant by participants in a sequencing study
Jennifer M Taber, William M P Klein, Katie L Lewis, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
September 7, 2019
Thrombosis risk factors in PIK3CA-related overgrowth spectrum and Proteus syndrome
Kim M Keppler-Noreuil, Jay Lozier, Neal Oden, et al.
Nature Genetics
|
May 10, 2000
Mutation of a gene encoding a putative chaperonin causes McKusick-Kaufman syndrome
D L Stone, A Slavotinek, G G Bouffard, et al.
BMC Medical Genetics
|
July 29, 2011
Brain tissue- and region-specific abnormalities on volumetric MRI scans in 21 patients with Bardet-Biedl syndrome (BBS)
Kim M Keppler-Noreuil, Catherine Blumhorst, Julie C Sapp, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 16, 2010
Recurrence risks for Bardet-Biedl syndrome: Implications of locus heterogeneity
Julie C Sapp, Darryl Nishimura, Jennifer J Johnston, et al.
American Journal of Medical Genetics. Part A
|
May 19, 2009
Molecular characterization of co-occurring Duchenne muscular dystrophy and X-linked oculo-facio-cardio-dental syndrome in a girl
Yong-hui Jiang, Ping Fang, Adekunle M Adesina, et al.
Page
of 48