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	1.	Response to reference ranges for lymphocyte subsets in adults from western India: influence of sex, age and method of enumeration. [electronic resource] by Tamhankar, Parag M Producer: 20110621 In: Indian journal of medical sciences vol. 63 Availability: No items available. Save to lists Add to cart (remove)
	2.	'Beehive-like'appearance in thoracic tuberculous lymphadenopathy. [electronic resource] by Tamhankar, Parag M Sangoi, Manoj Publication details: Journal of family medicine and primary care Jan 2020 In: Journal of family medicine and primary care vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Clinical profile and molecular diagnosis in patients of facioscapulohumeral dystrophy from Indian subcontinent. [electronic resource] by Tamhankar, Parag M Phadke, Shubha R Producer: 20101007 In: Neurology India vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Can Indian classical instrumental music reduce pain felt during venepuncture? [electronic resource] by Tamhankar, Parag M Chennuri, Vasundhara S Producer: 20101108 In: Indian journal of pediatrics vol. 77 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Rubinstein Taybi Syndrome in an Indian Child due to EP300 Gene Mutation. [electronic resource] by Tamhankar, Parag M Merchant, Rashid Shah, Ami Producer: 20170207 In: Indian journal of pediatrics vol. 83 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Cutaneous mastocytosis. Getting beneath the skin of the issue: a case report. [electronic resource] by Tamhankar, Parag M Suvarna, Jyoti Deshmukh, Chandrahas T Producer: 20121002 In: Cases journal vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Hemorrhagic pleural effusion: can it be scurvy? [electronic resource] by Suvarna, Jyoti Tamhankar, Parag M Deshmukh, C T Producer: 20071217 In: Indian journal of pediatrics vol. 74 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Macrocephaly in association with pontocerebellar hypoplasia type 1: a paradox. [electronic resource] by Tamhankar, Parag M Suvarna, Jyoti C Deshmukh, Chandrahas T Producer: 20090526 In: Indian journal of medical sciences vol. 63 Availability: No items available. Save to lists Add to cart (remove)
	9.	Identification of DKC1 gene mutation in an Indian patient. [electronic resource] by Tamhankar, Parag M Zhao, Meina Kanegane, Hirokazu Phadke, Shubha R Producer: 20100914 In: Indian journal of pediatrics vol. 77 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Profile of patients with Von Gierke disease from India. [electronic resource] by Tamhankar, Parag M Boggula, Vijayraju Girisha, K M Phadke, Shubha R Producer: 20121002 In: Indian pediatrics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	A novel beta-globin mutation (HBB:c.107A>G; or codon 35 beta (A-->G)) at alpha-beta chain interfaces. [electronic resource] by Kumar, Ravindra Tamhankar, Parag M Panigrahi, Inusha Dalal, Ashwin Agarwal, Sarita Producer: 20091123 In: Annals of hematology vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Clinical, biochemical and mutation profile in Indian patients with Sandhoff disease. [electronic resource] by Tamhankar, Parag M Mistri, Mehul Kondurkar, Pratima Sanghavi, Daksha Sheth, Jayesh Producer: 20170206 In: Journal of human genetics vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Neonatal severe hyperparathyroidism due to compound heterozygous mutation of calcium sensing receptor (CaSR) gene presenting as encephalopathy. [electronic resource] by Kulkarni, Abhishek Mohite, Mahesh Vijaykumar, Ramaa Bansode, Prasanna Murade, Sachin Tamhankar, Parag M Producer: 20160928 In: Indian journal of pediatrics vol. 81 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Genetic predisposition of E-selectin gene (S128R) polymorphism in patients with coronary artery disease (CAD). [electronic resource] by Tripathi, Rajneesh Singh, Prabhat Kumar Tewari, Satyendra Tamhankar, Parag M Ramesh, Venkataraman Agarwal, Sarita Producer: 20100201 In: The Indian journal of medical research vol. 130 Availability: No items available. Save to lists Add to cart (remove)
	15.	Mutation analysis of mitogen activated protein kinase 1 gene in Indian cases of 46,XY disorder of sex development. [electronic resource] by Das, Dhanjit Kumar Rahate, Subodh G Mehta, Bhakti P Gawde, Harshavardhan M Tamhankar, Parag M Producer: 20140205 In: Indian journal of human genetics vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Prevention of homozygous beta thalassemia by premarital screening and prenatal diagnosis in India. [electronic resource] by Tamhankar, Parag M Agarwal, Sarita Arya, Vandana Kumar, Ravindra Gupta, U R Agarwal, S S Producer: 20090515 In: Prenatal diagnosis vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Identification of novel mutations in STAR gene in patients with lipoid congenital adrenal hyperplasia: a first report from India. [electronic resource] by Vasudevan, Lakshmi Joshi, Rajesh Das, Dhanjit Kumar Rao, Sudha Sanghavi, Daksha Babu, Shiny Tamhankar, Parag M Producer: 20140110 In: Journal of clinical research in pediatric endocrinology vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Clinical applications and implications of common and founder mutations in Indian subpopulations. [electronic resource] by Ankala, Arunkanth Tamhankar, Parag M Valencia, C Alexander Rayam, Krishna K Kumar, Manisha M Hegde, Madhuri R Producer: 20150910 In: Human mutation vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Identification of novel mutations in HEXA gene in children affected with Tay Sachs disease from India. [electronic resource] by Mistri, Mehul Tamhankar, Parag M Sheth, Frenny Sanghavi, Daksha Kondurkar, Pratima Patil, Swapnil Idicula-Thomas, Susan Gupta, Sarita Sheth, Jayesh Producer: 20121212 In: PloS one vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Identification of novel ROR2 gene mutations in Indian children with Robinow syndrome. [electronic resource] by Tamhankar, Parag M Vasudevan, Lakshmi Kondurkar, Shweta Yashaswini, K Agarwalla, Sunil Kumar Nair, Mohandas Ramkumar, T V Chaubal, Nitin Chennuri, Vasundhara Sridhar Producer: 20150126 In: Journal of clinical research in pediatric endocrinology vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 24 results.