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Deepti Babu

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

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Journal of Genetic Counseling|November 22, 2019
Artificial intelligence in genetic services delivery: Utopia or apocalypse?Elizabeth Kearney, Antonina Wojcik, Deepti Babu
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|March 8, 2018
The future is now: Technology's impact on the practice of genetic counselingErynn S Gordon, Deepti Babu, Dawn A Laney
Personalized Medicine|May 18, 2018
Challenges in the codevelopment of companion diagnosticsMathew W Moore, Deepti Babu, Philip D Cotter
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|March 4, 2008
Extraocular muscle hypertrophy in myotonia congenitaBradley Wakeman, Deepti Babu, Jack Tarleton, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|October 21, 2009
Extraocular muscle hypertrophy in myotonia congenita: Mutation identified in the SCN4A gene (V445M)Bradley Wakeman, Ian M MacDonald, Ieke Ginjaar, et al.
Journal of Genetic Counseling|March 9, 2022
National Society of Genetic Counselors' Board of Directors response to Myers et al. 'A report of the AGCPD task force to evaluate associations between select admissions requirements, demographics, and performance on ABGC certification examination'Heather Zierhut, Leila Jamal, Sara Riordan, et al.
American Journal of Medical Genetics. Part A|January 18, 2006
Novel clinical features in a child with partial deletion of chromosome 11 [del(11)(q24.2)]: further evidence for phenotypic heterogeneityPhilip F Giampietro, Deepti Babu, Carrie A Zabel, et al.
American Journal of Medical Genetics. Part A|December 31, 2003
New syndrome: focal dermal hypoplasia, morning glory anomaly, and polymicrogyriaPhilip F Giampietro, Deepti Babu, Monica A Koehn, et al.
Plos One|September 10, 2014
Genitourinary defects associated with genomic deletions in 2p15 encompassing OTX1Carolina J Jorgez, Jill A Rosenfeld, Nathan R Wilken, et al.
Human Genetics|July 30, 2011
High-resolution array CGH defines critical regions and candidate genes for microcephaly, abnormalities of the corpus callosum, and seizure phenotypes in patients with microdeletions of 1q43q44Blake C Ballif, Jill A Rosenfeld, Ryan Traylor, et al.
Pageof 1

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

Sort By:
Pageof 1
Journal of Genetic Counseling|November 22, 2019
Artificial intelligence in genetic services delivery: Utopia or apocalypse?Elizabeth Kearney, Antonina Wojcik, Deepti Babu
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|March 8, 2018
The future is now: Technology's impact on the practice of genetic counselingErynn S Gordon, Deepti Babu, Dawn A Laney
Personalized Medicine|May 18, 2018
Challenges in the codevelopment of companion diagnosticsMathew W Moore, Deepti Babu, Philip D Cotter
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|March 4, 2008
Extraocular muscle hypertrophy in myotonia congenitaBradley Wakeman, Deepti Babu, Jack Tarleton, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|October 21, 2009
Extraocular muscle hypertrophy in myotonia congenita: Mutation identified in the SCN4A gene (V445M)Bradley Wakeman, Ian M MacDonald, Ieke Ginjaar, et al.
Journal of Genetic Counseling|March 9, 2022
National Society of Genetic Counselors' Board of Directors response to Myers et al. 'A report of the AGCPD task force to evaluate associations between select admissions requirements, demographics, and performance on ABGC certification examination'Heather Zierhut, Leila Jamal, Sara Riordan, et al.
American Journal of Medical Genetics. Part A|January 18, 2006
Novel clinical features in a child with partial deletion of chromosome 11 [del(11)(q24.2)]: further evidence for phenotypic heterogeneityPhilip F Giampietro, Deepti Babu, Carrie A Zabel, et al.
American Journal of Medical Genetics. Part A|December 31, 2003
New syndrome: focal dermal hypoplasia, morning glory anomaly, and polymicrogyriaPhilip F Giampietro, Deepti Babu, Monica A Koehn, et al.
Plos One|September 10, 2014
Genitourinary defects associated with genomic deletions in 2p15 encompassing OTX1Carolina J Jorgez, Jill A Rosenfeld, Nathan R Wilken, et al.
Human Genetics|July 30, 2011
High-resolution array CGH defines critical regions and candidate genes for microcephaly, abnormalities of the corpus callosum, and seizure phenotypes in patients with microdeletions of 1q43q44Blake C Ballif, Jill A Rosenfeld, Ryan Traylor, et al.
Pageof 1