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G Shashidhar Pai

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

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Indian Journal of Pediatrics|April 10, 2017
Genetic counseling in pediatric practiceG Shashidhar Pai
Indian Pediatrics|June 4, 2010
Developmental delay timely identification and assessmentJennifer K Poon, Angela C LaRosa, G Shashidhar Pai
American Journal of Medical Genetics|December 31, 1997
Fragile X syndrome and deletions in FMR1: new case and review of the literatureL S Hammond, M M Macias, J C Tarleton, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|April 2, 2005
Mosaic duplication 1(q11q44) in an infant with nephroblastomatosis and mineralization of extraplacental membranesLydia R Christiansen, Janice M Lage, Daynna J Wolff, et al.
JIMD Reports|May 12, 2021
[<sup>13</sup>C]-galactose breath test in a patient with galactokinase deficiency and spastic diparesisCan Ficicioglu, Didem Demirbas, Britt Derks, et al.
American Journal of Medical Genetics. Part A|January 8, 2005
Mutations in POMT1 are found in a minority of patients with Walker-Warburg syndromeSophie C Currier, Christine K Lee, Bernard S Chang, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|August 3, 2005
Characterization of a recurrent germ line mutation of the E-cadherin gene: implications for genetic testing and clinical managementGianpaolo Suriano, Sandie Yew, Paulo Ferreira, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 12, 2019
Variants in TCF20 in neurodevelopmental disability: description of 27 new patients and review of literatureErin Torti, Boris Keren, Elizabeth E Palmer, et al.
Pageof 1

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

Sort By:
Pageof 1
Indian Journal of Pediatrics|April 10, 2017
Genetic counseling in pediatric practiceG Shashidhar Pai
Indian Pediatrics|June 4, 2010
Developmental delay timely identification and assessmentJennifer K Poon, Angela C LaRosa, G Shashidhar Pai
American Journal of Medical Genetics|December 31, 1997
Fragile X syndrome and deletions in FMR1: new case and review of the literatureL S Hammond, M M Macias, J C Tarleton, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|April 2, 2005
Mosaic duplication 1(q11q44) in an infant with nephroblastomatosis and mineralization of extraplacental membranesLydia R Christiansen, Janice M Lage, Daynna J Wolff, et al.
JIMD Reports|May 12, 2021
[<sup>13</sup>C]-galactose breath test in a patient with galactokinase deficiency and spastic diparesisCan Ficicioglu, Didem Demirbas, Britt Derks, et al.
American Journal of Medical Genetics. Part A|January 8, 2005
Mutations in POMT1 are found in a minority of patients with Walker-Warburg syndromeSophie C Currier, Christine K Lee, Bernard S Chang, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|August 3, 2005
Characterization of a recurrent germ line mutation of the E-cadherin gene: implications for genetic testing and clinical managementGianpaolo Suriano, Sandie Yew, Paulo Ferreira, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 12, 2019
Variants in TCF20 in neurodevelopmental disability: description of 27 new patients and review of literatureErin Torti, Boris Keren, Elizabeth E Palmer, et al.
Pageof 1