Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Tarachandra

Showing results (1-10 of 8) with videos related to

Pageof 1
Sort By:
The Journal of the Louisiana State Medical Society : Official Organ of the Louisiana State Medical Society|June 13, 2012
Idiopathic proximal urea cycle disorder presenting as severe pulmonary hypertension in a neonate--a case reportDinesh Singh, Olugbenga Akingbola, Meenakshi Dutta, et al.
Journal of the Indian Medical Association|October 16, 1973
Chronic lingual abscessTarachandra, R D Srivastava, K N Singh
Bioengineering (Basel, Switzerland)|March 28, 2025
Bringing Precision to Pediatric Care: Explainable AI in Predicting No-Show Trends Before and During the COVID-19 PandemicQuincy A Hathaway, Naveena Yanamala, TaraChandra Narumanchi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 2, 2025
A primer on regulation of laboratory-developed testing procedures: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG)Marco L Leung, Raymond C Caylor, Olivia D'Annibale, et al.
Global Medical Genetics|July 15, 2025
Hemizygous contiguous gene deletion within Xq28 that includes BCAP31, ABCD1, SRPK3 and SSR4: case report and literature reviewJoan Chern-Hui Lien, Vinay D Chandrasekaran, Tarachandra M Narumanchi, et al.
The Journal of Molecular Diagnostics : JMD|January 23, 2010
Genome-wide oligonucleotide array comparative genomic hybridization for etiological diagnosis of mental retardation: a multicenter experience of 1499 clinical casesBixia Xiang, Hongbo Zhu, Yiping Shen, et al.
American Journal of Medical Genetics. Part A|February 27, 2020
Expanding the spectrum of CEP55-associated disease to viable phenotypesElizabeth S Barrie, Eline Overwater, Mieke M van Haelst, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 31, 2024
Expanding the phenotype and genotype spectrum of TAOK1 neurodevelopmental disorder and delineating TAOK2 neurodevelopmental disorderNour Elkhateeb, Renarta Crookes, Michael Spiller, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
The Journal of the Louisiana State Medical Society : Official Organ of the Louisiana State Medical Society|June 13, 2012
Idiopathic proximal urea cycle disorder presenting as severe pulmonary hypertension in a neonate--a case reportDinesh Singh, Olugbenga Akingbola, Meenakshi Dutta, et al.
Journal of the Indian Medical Association|October 16, 1973
Chronic lingual abscessTarachandra, R D Srivastava, K N Singh
Bioengineering (Basel, Switzerland)|March 28, 2025
Bringing Precision to Pediatric Care: Explainable AI in Predicting No-Show Trends Before and During the COVID-19 PandemicQuincy A Hathaway, Naveena Yanamala, TaraChandra Narumanchi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 2, 2025
A primer on regulation of laboratory-developed testing procedures: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG)Marco L Leung, Raymond C Caylor, Olivia D'Annibale, et al.
Global Medical Genetics|July 15, 2025
Hemizygous contiguous gene deletion within Xq28 that includes BCAP31, ABCD1, SRPK3 and SSR4: case report and literature reviewJoan Chern-Hui Lien, Vinay D Chandrasekaran, Tarachandra M Narumanchi, et al.
The Journal of Molecular Diagnostics : JMD|January 23, 2010
Genome-wide oligonucleotide array comparative genomic hybridization for etiological diagnosis of mental retardation: a multicenter experience of 1499 clinical casesBixia Xiang, Hongbo Zhu, Yiping Shen, et al.
American Journal of Medical Genetics. Part A|February 27, 2020
Expanding the spectrum of CEP55-associated disease to viable phenotypesElizabeth S Barrie, Eline Overwater, Mieke M van Haelst, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 31, 2024
Expanding the phenotype and genotype spectrum of TAOK1 neurodevelopmental disorder and delineating TAOK2 neurodevelopmental disorderNour Elkhateeb, Renarta Crookes, Michael Spiller, et al.
Pageof 1