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Datar, Chaitanya
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1

Lysosomal storage disorders identified in adult population ..:

Sheth, Jayesh ; Nair, Aadhira ; Bhavsar, Riddhi...
JIMD Reports.  65 (2024)  2 - p. 85-101 , 2024
Link: https://doi.org/10.1002/..
 
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2

Burden of rare genetic disorders in India: twenty-two years..:

Sheth, Jayesh ; Nair, Aadhira ; Sheth, Frenny...
Orphanet Journal of Rare Diseases.  19 (2024)  1 - p. , 2024
Link: https://doi.org/10.1186/..
 
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3

Late infantile form of multiple sulfatase deficiency with a..:

Sheth, Jayesh ; Shah, Siddharth ; Datar, Chaitanya...
BMC Pediatrics.  23 (2023)  1 - p. , 2023
Link: https://doi.org/10.1186/..
 
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4

Genotype-phenotype spectrum of 130 unrelated Indian familie..:

Agrawal, Neha ; Verma, Gaurav ; Saxena, Deepti...
European Journal of Medical Genetics.  65 (2022)  3 - p. 104447 , 2022
Link: https://doi.org/10.1016/..
 
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5

First reported cases with Xia‐Gibbs syndrome from India har..:

Danda, Sumita ; Datar, Chaitanya ; Kher, Archana...
American Journal of Medical Genetics Part A.  188 (2022)  8 - p. 2501-2504 , 2022
Link: https://doi.org/10.1002/..
 
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6

Pseudoachondroplasia: Phenotype and genotype in 11 Indian p..:

Jacob, Prince ; Bhavani, Gandham Sri Lakshmi ; Shah, Hitesh...
American Journal of Medical Genetics Part A.  188 (2021)  3 - p. 751-759 , 2021
Link: https://doi.org/10.1002/..
 
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7

Identification and characterization of 30 novel pathogenic ..:

Pasumarthi, Divya ; Gupta, Neerja ; Sheth, Jayesh...
Journal of Human Genetics.  65 (2020)  11 - p. 971-984 , 2020
Link: https://doi.org/10.1038/..
 
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8

Elucidation of the phenotypic spectrum and genetic landscap..:

Boonsawat, Paranchai ; Joset, Pascal ; Steindl, Katharina...
Genetics in Medicine.  21 (2019)  9 - p. 2043-2058 , 2019
Link: https://doi.org/10.1038/..
 
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9

Spectrum of ARSA variations in Asian Indian patients with A..:

Narayanan, Dhanya Lakshmi ; Matta, Divya ; Gupta, Neerja...
Journal of Human Genetics.  64 (2019)  4 - p. 323-331 , 2019
Link: https://doi.org/10.1038/..
 
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10

Gaucher disease: single gene molecular characterization of ..:

Sheth, Jayesh ; Bhavsar, Riddhi ; Mistri, Mehul...
BMC Medical Genetics.  20 (2019)  1 - p. , 2019
Link: https://doi.org/10.1186/..
 
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11

Ring chromosome 20 syndrome – A rare chromosomal cause of r..:

Kalane, Umesh ; Datar, Chaitanya ; Kalane, Shilpa
International Journal of Epilepsy.  4 (2017)  1 - p. 087-089 , 2017
Link: https://doi.org/10.1016/..
 
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12

GM2 gangliosidosis AB variant: novel mutation from India – ..:

Sheth, Jayesh ; Datar, Chaitanya ; Mistri, Mehul...
BMC Pediatrics.  16 (2016)  1 - p. , 2016
Link: https://doi.org/10.1186/..
 
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13

Recurrent and novel GLB1 mutations in India:

Bidchol, Abdul Mueed ; Dalal, Ashwin ; Trivedi, Rakesh...
Gene.  567 (2015)  2 - p. 173-181 , 2015
Link: https://doi.org/10.1016/..
 
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14

Lysosomal storage disorders in Indian children with neurore..:

Sheth, Jayesh ; Mistri, Mehul ; Bhavsar, Riddhi...
Indian Pediatrics.  52 (2015)  12 - p. 1029-1033 , 2015
Link: https://doi.org/10.1007/..
 
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15

Expanding the spectrum of HEXA mutations in Indian patients..:

Sheth, Jayesh ; Mistri, Mehul ; Datar, Chaitanya...
Molecular Genetics and Metabolism Reports.  1 (2014)  - p. 425-430 , 2014
Link: https://doi.org/10.1016/..
 
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