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Yuri A Zarate

Showing results (1-10 of 103) with videos related to

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Case Reports in Genetics|August 9, 2020
Managing Sleep and Behavioral Problems in a Preschooler with <i>SATB2</i>-Associated SyndromeNihit Kumar, Yuri A Zarate
Acta Neurologica Belgica|February 2, 2019
Widening phenotypic spectrum of GABBR2 mutationDebopam Samanta, Yuri A Zarate
American Journal of Medical Genetics. Part A|June 18, 2009
Twin-twin transfusion resulting in fetal cell contamination in Beckwith-Wiedemann syndromeYuri A Zarate, Robert J Hopkin
American Journal of Medical Genetics. Part A|October 25, 2016
SATB2-associated syndrome: Mechanisms, phenotype, and practical recommendationsYuri A Zarate, Jennifer L Fish
Lancet (London, England)|October 23, 2008
Fabry's diseaseYuri A Zarate, Robert J Hopkin
European Journal of Medical Genetics|September 24, 2013
Description of another case of 3q26.33-3q27.2 microdeletion supports a recognizable phenotypeYuri A Zarate, Carla Bell, Brad Schaefer
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|May 1, 2018
Combined Tongue-Palate Fusion With Alveolar Bands in a Patient With Pierre Robin Sequence and Van der Woude SyndromeAlexa Robbins, Yuri A Zarate, Larry D Hartzell
Acta Neurologica Belgica|April 5, 2016
An infant with ash-leaf and café au lait spots: a case of double phakomatosisDebopam Samanta, Katherine B Bosanko, Yuri A Zarate
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|May 9, 2014
Radioulnar Synostosis and Brain Abnormalities in a Patient With 17q21.31 Microdeletion Involving EFTUD2Yuri A Zarate, Carla Bell, G Bradley Schaefer
Special Care in Dentistry : Official Publication of the American Association of Hospital Dentists, the Academy of Dentistry for the Handicapped, and the American Society for Geriatric Dentistry|January 17, 2019
SATB2-associated syndrome (SAS) and associated dental findingsJohn Scott, Chad Adams, Stephen Beetstra, et al.
Pageof 11

Showing results (1-10 of 103) with videos related to

Sort By:
Pageof 11
Case Reports in Genetics|August 9, 2020
Managing Sleep and Behavioral Problems in a Preschooler with <i>SATB2</i>-Associated SyndromeNihit Kumar, Yuri A Zarate
Acta Neurologica Belgica|February 2, 2019
Widening phenotypic spectrum of GABBR2 mutationDebopam Samanta, Yuri A Zarate
American Journal of Medical Genetics. Part A|June 18, 2009
Twin-twin transfusion resulting in fetal cell contamination in Beckwith-Wiedemann syndromeYuri A Zarate, Robert J Hopkin
American Journal of Medical Genetics. Part A|October 25, 2016
SATB2-associated syndrome: Mechanisms, phenotype, and practical recommendationsYuri A Zarate, Jennifer L Fish
Lancet (London, England)|October 23, 2008
Fabry's diseaseYuri A Zarate, Robert J Hopkin
European Journal of Medical Genetics|September 24, 2013
Description of another case of 3q26.33-3q27.2 microdeletion supports a recognizable phenotypeYuri A Zarate, Carla Bell, Brad Schaefer
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|May 1, 2018
Combined Tongue-Palate Fusion With Alveolar Bands in a Patient With Pierre Robin Sequence and Van der Woude SyndromeAlexa Robbins, Yuri A Zarate, Larry D Hartzell
Acta Neurologica Belgica|April 5, 2016
An infant with ash-leaf and café au lait spots: a case of double phakomatosisDebopam Samanta, Katherine B Bosanko, Yuri A Zarate
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|May 9, 2014
Radioulnar Synostosis and Brain Abnormalities in a Patient With 17q21.31 Microdeletion Involving EFTUD2Yuri A Zarate, Carla Bell, G Bradley Schaefer
Special Care in Dentistry : Official Publication of the American Association of Hospital Dentists, the Academy of Dentistry for the Handicapped, and the American Society for Geriatric Dentistry|January 17, 2019
SATB2-associated syndrome (SAS) and associated dental findingsJohn Scott, Chad Adams, Stephen Beetstra, et al.
Pageof 11