E-LIB Suche - Ergebnisse für: Tamhankar, Parag

1

Novel Consensus Splice Site Pathogenic Variation in THOC2 G..:

Tamhankar, Vasundhara ; Tamhankar, Parag ; Chaubal, Rajas..
Cureus. , 2021

Link: https://doi.org/10.7759/..

2

Character Recognition of Offline Handwritten Marathi Docume..:

, In: Communications in Computer and Information Science; Recent Trends in Image Processing and Pattern Recognition,

Tamhankar, Parag A. ; Masalkar, Krishnat D. ; Kolhe, Satish R. - p. 478-487 , 2021

Link: https://doi.org/10.1007/..

3

Prenatal Diagnosis for Primary Immunodeficiency Disorders—A..:

Yadav, Reetika Malik ; Gupta, Maya ; Dalvi, Aparna...
Frontiers in Immunology. 11 (2020) - p. , 2020

Link: https://doi.org/10.3389/..

4

A Novel Approach for Character Segmentation of Offline Hand..:

Tamhankar, Parag A. ; Masalkar, Krishnat D. ; kolhe, Satish R.
Procedia Computer Science. 171 (2020) - p. 179-187 , 2020

Link: https://doi.org/10.1016/..

5

Erratum: Novel mutations in the glucocerebrosidase gene of ..:

Ankleshwaria, Chitra ; Mistri, Mehul ; Bavdekar, Ashish...
Journal of Human Genetics. 60 (2015) 5 - p. 285-285 , 2015

Link: https://doi.org/10.1038/..

6

Prenatal diagnosis in India is not limited to sex selection:

Dalal, Ashwin B. ; Ranganath, Prajnya ; Phadke, Shubha R....
Genetics in Medicine. 17 (2015) 1 - p. 88 , 2015

Link: https://doi.org/10.1038/..

7

Novel mutations in the glucocerebrosidase gene of Indian pa..:

Ankleshwaria, Chitra ; Mistri, Mehul ; Bavdekar, Ashish...
Journal of Human Genetics. 59 (2014) 4 - p. 223-228 , 2014

Link: https://doi.org/10.1038/..

8

Molecular basis of lysosomal storage disorders in India:

Kondurkar, Shweta P ; Tamhankar, Parag ; Kondurkar, Pratima..
Molecular Cytogenetics. 7 (2014) Suppl 1 - p. P130 , 2014

Link: https://doi.org/10.1186/..

9

Case Reports:

Ramzan, Mohammed ; Yadav, Satya Prakash ; Joshi, Rajesh...
Indian Pediatrics. 51 (2014) 5 - p. 397-406 , 2014

Link: https://doi.org/10.1007/..

10

Molecular diagnosis of genodermatoses in india:

Tamhankar, Parag
Molecular Cytogenetics. 7 (2014) Suppl 1 - p. I18 , 2014

Link: https://doi.org/10.1186/..

11

Lack of association of primary iron overload and common HFE..:

Jain, Shalu ; Agarwal, Sarita ; Tamhankar, Parag..
Indian Journal of Gastroenterology. 30 (2011) 4 - p. 161-165 , 2011

Link: https://doi.org/10.1007/..

12

Exome sequencing and microarray identified a novel large ex..:

Kumar, C. P. Ravi ; Tamhankar, Parag M. ; Manohar, Radhika...
Journal of Genetics. 102 (2022) 1 - p. , 2022

Link: https://doi.org/10.1007/..

13

Spectrum of mutations in the SMPD1 gene in Asian Indian pat..:

Ranganath, Prajnya ; Matta, Divya ; Bhavani, Gandham SriLakshmi...
American Journal of Medical Genetics Part A. 173 (2017) 3 - p. 829-829 , 2017

Link: https://doi.org/10.1002/..

14

Spectrum of SMPD1 mutations in Asian‐Indian patients with a..:

Ranganath, Prajnya ; Matta, Divya ; Bhavani, Gandham SriLakshmi...
American Journal of Medical Genetics Part A. 170 (2016) 10 - p. 2719-2730 , 2016

Link: https://doi.org/10.1002/..

15

Rubinstein Taybi Syndrome in an Indian Child due to EP300 G..:

Tamhankar, Parag M. ; Merchant, Rashid ; Shah, Ami
The Indian Journal of Pediatrics. 83 (2015) 5 - p. 473-474 , 2015

Link: https://doi.org/10.1007/..