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Batsal Devkota

Showing results (11-20 of 29) with videos related to

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Journal of Assisted Reproduction and Genetics|June 11, 2014
Lack of association of KATNAL1 gene sequence variants and azoospermia in humansAnastasia M Fedick, Kyle Eckert, Katharine Thompson, et al.
Human Genetics|March 21, 2021
Genome-first approach to rare EYA4 variants and cardio-auditory phenotypes in adultsShadi Ahmadmehrabi, Binglan Li, Joseph Park, et al.
American Journal of Hematology|September 30, 2017
Utility and limitations of exome sequencing in the molecular diagnosis of pediatric inherited platelet disordersEdward J Romasko, Batsal Devkota, Sawona Biswas, et al.
The Journal of Pediatrics|March 22, 2022
Molecular Mechanisms Contributing to the Etiology of Congenital Diaphragmatic Hernia: A Review and Novel CasesOlivia L Katz, K Taylor Wild, Deborah McEldrew, et al.
European Journal of Human Genetics : EJHG|January 11, 2019
Rapid and accurate interpretation of clinical exomes using Phenoxome: a computational phenotype-driven approachChao Wu, Batsal Devkota, Perry Evans, et al.
Pediatrics|February 28, 2020
A Centralized Approach for Practicing Genomic MedicineSawona Biswas, Livija Medne, Batsal Devkota, et al.
Nucleic Acids Research|October 12, 2010
EMDataBank.org: unified data resource for CryoEMCatherine L Lawson, Matthew L Baker, Christoph Best, et al.
The Journal of Pediatrics|July 20, 2023
Comprehensive Gene Panel Testing for Hearing Loss in Children: Understanding Factors Influencing Diagnostic YieldNobuko Yamamoto, Jorune Balciuniene, Tiffiney Hartman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 17, 2018
Utility and limitations of exome sequencing as a genetic diagnostic tool for children with hearing lossSarah Sheppard, Sawona Biswas, Mindy H Li, et al.
Structure (London, England : 1993)|February 14, 2012
Outcome of the first electron microscopy validation task force meetingRichard Henderson, Andrej Sali, Matthew L Baker, et al.
Pageof 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
Journal of Assisted Reproduction and Genetics|June 11, 2014
Lack of association of KATNAL1 gene sequence variants and azoospermia in humansAnastasia M Fedick, Kyle Eckert, Katharine Thompson, et al.
Human Genetics|March 21, 2021
Genome-first approach to rare EYA4 variants and cardio-auditory phenotypes in adultsShadi Ahmadmehrabi, Binglan Li, Joseph Park, et al.
American Journal of Hematology|September 30, 2017
Utility and limitations of exome sequencing in the molecular diagnosis of pediatric inherited platelet disordersEdward J Romasko, Batsal Devkota, Sawona Biswas, et al.
The Journal of Pediatrics|March 22, 2022
Molecular Mechanisms Contributing to the Etiology of Congenital Diaphragmatic Hernia: A Review and Novel CasesOlivia L Katz, K Taylor Wild, Deborah McEldrew, et al.
European Journal of Human Genetics : EJHG|January 11, 2019
Rapid and accurate interpretation of clinical exomes using Phenoxome: a computational phenotype-driven approachChao Wu, Batsal Devkota, Perry Evans, et al.
Pediatrics|February 28, 2020
A Centralized Approach for Practicing Genomic MedicineSawona Biswas, Livija Medne, Batsal Devkota, et al.
Nucleic Acids Research|October 12, 2010
EMDataBank.org: unified data resource for CryoEMCatherine L Lawson, Matthew L Baker, Christoph Best, et al.
The Journal of Pediatrics|July 20, 2023
Comprehensive Gene Panel Testing for Hearing Loss in Children: Understanding Factors Influencing Diagnostic YieldNobuko Yamamoto, Jorune Balciuniene, Tiffiney Hartman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 17, 2018
Utility and limitations of exome sequencing as a genetic diagnostic tool for children with hearing lossSarah Sheppard, Sawona Biswas, Mindy H Li, et al.
Structure (London, England : 1993)|February 14, 2012
Outcome of the first electron microscopy validation task force meetingRichard Henderson, Andrej Sali, Matthew L Baker, et al.
Pageof 3