T. Geetha
发表
K. Thangaraj,
M. Faruq,
A. Nalini,
2022,
neurogenetics.
R. Chaudhary,
S. Seshagiri,
A. Peterson,
2022,
Advanced biology.
T. Sandmann,
U. Muthane,
R. Borgohain,
2023,
medRxiv.
S. Phadke,
K. Girisha,
S. Nampoothiri,
2022,
Journal of Medical Genetics.
M. Kabra,
B. Thelma,
R. Juyal,
2014,
Human mutation.
A. Mahadevan,
V. Ramprasad,
P. Kukkle,
2020,
Movement disorders clinical practice.
A. Mahadevan,
V. Ramprasad,
Thenral S. Geetha,
2020,
Movement disorders clinical practice.
A. Nalini,
K. Polavarapu,
S. Vengalil,
2022,
neurogenetics.
S. Zuberi,
S. Murugan,
J. Symonds,
2020,
Epilepsy & behavior reports.
S. Pandey,
C. Sankhla,
V. Ramprasad,
2019,
Parkinsonism & related disorders.
L. Lingappa,
S. Murugan,
Ramprasad Vedam,
2017,
Molecular genetics & genomic medicine.
S. Asthana,
R. Lochan,
Karthik K. Raichurkar,
2021,
Journal of clinical and experimental hepatology.
M. Desai,
A. Pandrowala,
V. Patel,
2020,
Journal of Pediatric Neurology.
Comprehensive laboratory diagnosis of Fanconi anaemia: comparison of cellular and molecular analysis
B. George,
G. Joshi,
A. Abraham,
2023,
Journal of Medical Genetics.
A. Sinha,
A. Bagga,
A. Seth,
2022,
Indian Journal of Pediatrics.
A. Sinha,
A. Bagga,
S. Nair,
2020,
Pediatric Nephrology.
O. Birk,
M. Kabra,
N. Gupta,
2022,
Annals of human genetics.