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Ganapathy, Aparna
31
results:
Search for persons
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Online (31)
Mediatypes
Articles (Online) (17)
Bookchapter (Online) (1)
OpenAccess-fulltext (13)
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1
Targeted Sequencing Detects Variants That May Contribute to..:
Mahadevan, Jayant
;
Sud, Reeteka
;
Nadella, Ravi Kumar
...
Indian Journal of Psychological Medicine. 44 (2021) 5 - p. 516-522 , 2021
Link:
https://doi.org/10.1177/..
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2
Charcot-Marie-Tooth disease type 2S: identical novel missen..:
Chandrasekharan, Soumya V.
;
Nair, Sruthi S.
;
Ganapathy, Aparna
..
Neurological Sciences. 43 (2021) 1 - p. 719-722 , 2021
Link:
https://doi.org/10.1007/..
?
3
Determining Cost-Optimal Next-Generation Sequencing Panels ..:
Katragadda, Shanmukh
;
Hall, Taryn O
;
Bettadapura, Radhakrishna
...
Clinical Chemistry. 67 (2021) 8 - p. 1122-1132 , 2021
Link:
https://doi.org/10.1093/..
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4
Lethal Cenani Lenz syndrome in two consecutive pregnancies:..:
Yesodharan, Dhanya
;
Krishnan, Vivek
;
Nair, Indu R.
...
American Journal of Medical Genetics Part A. 185 (2020) 2 - p. 620-624 , 2020
Link:
https://doi.org/10.1002/..
?
5
Lipoprotein Lipase Deficiency:
Kuthiroly, Shwetha
;
Yesodharan, Dhanya
;
Radhakrishnan, Natasha
...
The Indian Journal of Pediatrics. 88 (2020) 2 - p. 147-153 , 2020
Link:
https://doi.org/10.1007/..
?
6
Chronic Mucocutaneous Candidiasis in an Adolescent Boy Due ..:
Bhattad, Sagar
;
Dinakar, Chitra
;
Pinnamaraju, Haneesha
..
Journal of Clinical Immunology. 39 (2019) 6 - p. 596-599 , 2019
Link:
https://doi.org/10.1007/..
?
7
Multi-gene testing in neurological disorders showed an impr..:
Ganapathy, Aparna
;
Mishra, Avshesh
;
Soni, Megha Rani
...
Journal of Neurology. 266 (2019) 8 - p. 1919-1926 , 2019
Link:
https://doi.org/10.1007/..
?
8
Clinical and genetic analysis of Indian patients with NDP-r..:
Sudha, Dhandayuthapani
;
Ganapathy, Aparna
;
Mohan, Puja
...
International Ophthalmology. 38 (2017) 3 - p. 1251-1260 , 2017
Link:
https://doi.org/10.1007/..
?
9
Identification of Novel Mutations inABCA4Gene: Clinical and..:
Battu, Rajani
;
Verma, Anshuman
;
Hariharan, Ramesh
...
BioMed Research International. 2015 (2015) - p. 1-10 , 2015
Link:
https://doi.org/10.1155/..
?
10
Non-Syndromic Hearing Impairment in India: High Allelic Het..:
Ganapathy, Aparna
;
Pandey, Nishtha
;
Srisailapathy, C. R. Srikumari
...
PLoS ONE. 9 (2014) 1 - p. e84773 , 2014
Link:
https://doi.org/10.1371/..
?
11
1q42.12q42.2 Deletion in a Child with Midline Defects and H..:
Radha Rama Devi, Akella
;
Ganapathy, Aparna
;
Mannan, Ashraf U
..
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6528072/. , 2019
Link:
http://www.ncbi.nlm.nih...
?
12
Targeted sequencing of the DMD locus: A comprehensive diagn..:
Aravind, Sankaramoorthy
;
Ashley, Berty
;
Mannan, Ashraf
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6886143/. , 2019
Link:
http://www.ncbi.nlm.nih...
?
13
Identification of a case of SRD5A3-congenital disorder of g..:
Gupta, Neerja
;
Verma, Gaurav
;
Kabra, Madhulika
..
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6057243/. , 2018
Link:
http://www.ncbi.nlm.nih...
?
14
Non-Syndromic Hearing Impairment in India: high Allelic Het..:
Ganapathy, Aparna
;
Pandey, Nishtha
;
Srisailapathy, C. R. Srikumari
...
Plos One. -9 : 1 (2014), [10] p. -PLoS One. - 1932-6203. , 2014
Link:
http://hdl.handle.net/24..
?
15
Functional consequences of novel connexin 26 mutations asso..:
Mani, Ram Shankar
;
Ganapathy, Aparna
;
Jalvi, Rajeev
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2986212. , 2009
Link:
http://www.ncbi.nlm.nih...
1-15