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S Aggarwal

Showing results (331-340 of 344) with videos related to

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HGG Advances|April 1, 2021
TMEM218 dysfunction causes ciliopathies, including Joubert and Meckel syndromesJulie C Van De Weghe, Jessica L Giordano, Inge B Mathijssen, et al.
BMJ Open|July 4, 2024
Community perspective and healthcare assessment in malaria endemic states of India: a cross-sectional study protocolShrinivasa B M, Vani H C, Richa Singhal, et al.
The New England Journal of Medicine|December 11, 2012
Chromosomal microarray versus karyotyping for prenatal diagnosisRonald J Wapner, Christa Lese Martin, Brynn Levy, et al.
Clinical Journal of the American Society of Nephrology : CJASN|April 18, 2020
Pilot Study of Return of Genetic Results to Patients in Adult NephrologyJordan G Nestor, Maddalena Marasa, Hila Milo-Rasouly, et al.
ESMO Open|October 9, 2025
Pan-Asian adapted ESMO Clinical Practice Guidelines for the diagnosis, treatment and follow-up of patients with pancreatic cancerD Tai, T Conroy, J J X Lee, et al.
American Journal of Human Genetics|August 18, 2023
Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomaliesChelsea Lowther, Elise Valkanas, Jessica L Giordano, et al.
The New England Journal of Medicine|December 27, 2018
Diagnostic Utility of Exome Sequencing for Kidney DiseaseEmily E Groopman, Maddalena Marasa, Sophia Cameron-Christie, et al.
American Journal of Medical Genetics. Part A|September 9, 2018
Refining the phenotype associated with GNB1 mutations: Clinical data on 18 newly identified patients and review of the literatureParisa Hemati, Anya Revah-Politi, Haim Bassan, et al.
The Journal of the Association of Physicians of India|June 24, 2025
Bridging the Gap: Managing Hypertension in Indian Patients with Metabolic SyndromeJ S Hiremath, G S Wander, A Dasbiswas, et al.
American Journal of Human Genetics|January 28, 2021
De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosisPatricia L Weng, Amar J Majmundar, Kamal Khan, et al.
Pageof 35

Showing results (331-340 of 344) with videos related to

Sort By:
Pageof 35
HGG Advances|April 1, 2021
TMEM218 dysfunction causes ciliopathies, including Joubert and Meckel syndromesJulie C Van De Weghe, Jessica L Giordano, Inge B Mathijssen, et al.
BMJ Open|July 4, 2024
Community perspective and healthcare assessment in malaria endemic states of India: a cross-sectional study protocolShrinivasa B M, Vani H C, Richa Singhal, et al.
The New England Journal of Medicine|December 11, 2012
Chromosomal microarray versus karyotyping for prenatal diagnosisRonald J Wapner, Christa Lese Martin, Brynn Levy, et al.
Clinical Journal of the American Society of Nephrology : CJASN|April 18, 2020
Pilot Study of Return of Genetic Results to Patients in Adult NephrologyJordan G Nestor, Maddalena Marasa, Hila Milo-Rasouly, et al.
ESMO Open|October 9, 2025
Pan-Asian adapted ESMO Clinical Practice Guidelines for the diagnosis, treatment and follow-up of patients with pancreatic cancerD Tai, T Conroy, J J X Lee, et al.
American Journal of Human Genetics|August 18, 2023
Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomaliesChelsea Lowther, Elise Valkanas, Jessica L Giordano, et al.
The New England Journal of Medicine|December 27, 2018
Diagnostic Utility of Exome Sequencing for Kidney DiseaseEmily E Groopman, Maddalena Marasa, Sophia Cameron-Christie, et al.
American Journal of Medical Genetics. Part A|September 9, 2018
Refining the phenotype associated with GNB1 mutations: Clinical data on 18 newly identified patients and review of the literatureParisa Hemati, Anya Revah-Politi, Haim Bassan, et al.
The Journal of the Association of Physicians of India|June 24, 2025
Bridging the Gap: Managing Hypertension in Indian Patients with Metabolic SyndromeJ S Hiremath, G S Wander, A Dasbiswas, et al.
American Journal of Human Genetics|January 28, 2021
De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosisPatricia L Weng, Amar J Majmundar, Kamal Khan, et al.
Pageof 35