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Katta Mohan Girisha

Showing results (1-10 of 58) with videos related to

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American Journal of Medical Genetics. Part A|February 9, 2021
Wiedemann-Rautenstrauch syndrome in an Indian patient with biallelic pathogenic variants in POLR3APurvi Majethia, Katta Mohan Girisha
Indian Pediatrics|February 26, 2021
Understanding Exome Sequencing: Tips for the PediatricianDhanya Lakshmi Narayanan, Katta Mohan Girisha
Indian Pediatrics|June 21, 2020
Genomic Testing for Diagnosis of Genetic Disorders in Children: Chromosomal Microarray and Next-Generation SequencingDhanya Lakshmi Narayanan, Katta Mohan Girisha
American Journal of Medical Genetics. Part A|October 12, 2020
Trichothiodystrophy type 4 in an Indian familyShruti Pande, Anju Shukla, Katta Mohan Girisha
Clinical Dysmorphology|November 24, 2020
Expanding the phenotype of PURA-related neurodevelopmental disorder: a close differential diagnosis of infantile hypotonia with psychomotor retardation and characteristic faciesShivani Mishra, Katta Mohan Girisha, Anju Shukla
Clinical Dysmorphology|March 24, 2009
Milder form of pachydermoperiostosis: a report of four casesKatta Mohan Girisha, Kausik Mandal, Shubha Rajendra Phadke
Clinical Dysmorphology|October 10, 2020
Mongolian spots in GM1 gangliosidosis: a pictorial reportShivani Mishra, Pranita Pai, Anusha Uttarilli, et al.
American Journal of Medical Genetics. Part A|January 12, 2013
Expanding the phenotype associated with 17q12 duplication: case report and review of the literatureTatjana Bierhals, Satish Babu Maddukuri, Kerstin Kutsche, et al.
Indian Pediatrics|February 19, 2015
White matter changes in GM1 gangliosidosisMoni Tuteja, Abdul Mueed Bidchol, Katta Mohan Girisha, et al.
Indian Journal of Pediatrics|October 16, 2013
A novel frameshift mutation in TWIST2 gene causing Setleis syndromeKatta Mohan Girisha, Abdul Mueed Bidchol, Murali Keshava Sarpangala, et al.
Pageof 6

Showing results (1-10 of 58) with videos related to

Sort By:
Pageof 6
American Journal of Medical Genetics. Part A|February 9, 2021
Wiedemann-Rautenstrauch syndrome in an Indian patient with biallelic pathogenic variants in POLR3APurvi Majethia, Katta Mohan Girisha
Indian Pediatrics|February 26, 2021
Understanding Exome Sequencing: Tips for the PediatricianDhanya Lakshmi Narayanan, Katta Mohan Girisha
Indian Pediatrics|June 21, 2020
Genomic Testing for Diagnosis of Genetic Disorders in Children: Chromosomal Microarray and Next-Generation SequencingDhanya Lakshmi Narayanan, Katta Mohan Girisha
American Journal of Medical Genetics. Part A|October 12, 2020
Trichothiodystrophy type 4 in an Indian familyShruti Pande, Anju Shukla, Katta Mohan Girisha
Clinical Dysmorphology|November 24, 2020
Expanding the phenotype of PURA-related neurodevelopmental disorder: a close differential diagnosis of infantile hypotonia with psychomotor retardation and characteristic faciesShivani Mishra, Katta Mohan Girisha, Anju Shukla
Clinical Dysmorphology|March 24, 2009
Milder form of pachydermoperiostosis: a report of four casesKatta Mohan Girisha, Kausik Mandal, Shubha Rajendra Phadke
Clinical Dysmorphology|October 10, 2020
Mongolian spots in GM1 gangliosidosis: a pictorial reportShivani Mishra, Pranita Pai, Anusha Uttarilli, et al.
American Journal of Medical Genetics. Part A|January 12, 2013
Expanding the phenotype associated with 17q12 duplication: case report and review of the literatureTatjana Bierhals, Satish Babu Maddukuri, Kerstin Kutsche, et al.
Indian Pediatrics|February 19, 2015
White matter changes in GM1 gangliosidosisMoni Tuteja, Abdul Mueed Bidchol, Katta Mohan Girisha, et al.
Indian Journal of Pediatrics|October 16, 2013
A novel frameshift mutation in TWIST2 gene causing Setleis syndromeKatta Mohan Girisha, Abdul Mueed Bidchol, Murali Keshava Sarpangala, et al.
Pageof 6