Spectrum of GJB2 gene variants in Indian children with non-syndromic hearing loss von Singh, Pawan, Sharma, Shipra, Ghosh, Manju, Shastri, Shivaram, Gupta, Neerja, Kabra, Madhulika

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Influence of MDR1 and CYP3A5 genetic polymorphisms on trough levels and therapeutic response of imatinib in newly diagnosed patients with chronic myeloid leukemia von Harivenkatesh, Natarajan, Kumar, Lalit, Bakhshi, Sameer, Sharma, Atul, Kabra, Madhulika, Velpandian, Thirumurthy, Gogia, Ajay, Shastri, Shivaram S., Biswas, Nihar Ranjan, Gupta, Yogendra Kumar

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Association of SPINK1 Gene Mutation and CFTR Gene Polymorphisms in Patients With Pancreas Divisum Presenting With Idiopathic Pancreatitis von Garg, Pramod Kumar, Khajuria, Rajni, Kabra, Madhulika, Shastri, Shivaram S

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Characterisation of mutations and genotype–phenotype correlation in cystic fibrosis: Experience from India von Shastri, Shivaram S, Kabra, Madhulika, Kabra, Sushil Kumar, Pandey, Ravindra M, Menon, P.S.N

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Carrier frequency of F508del mutation of cystic fibrosis in Indian population von Kapoor, Vishal, Shastri, Shivaram S., Kabra, Madhulika, Kabra, Sushil Kumar, Ramachandran, Vijaya, Arora, Sadhna, Balakrishnan, Prahlad, Deorari, Ashok Kumar, Paul, Vinod Kumar

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Idiopathic chronic pancreatitis in India: phenotypic characterisation and strong genetic susceptibility due to SPINK1 and CFTR gene mutations von Midha, Shallu, Khajuria, Rajni, Shastri, Shivaram, Kabra, Madhulika, Garg, Pramod Kumar

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Two functionals approach in DFT for the prediction of thermoelectric properties of Fe2ScX (X  =  P, As, Sb) full-Heusler compounds von Shastri, Shivprasad S, Pandey, Sudhir K

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Studying the lifetime of charge and heat carriers due to intrinsic scattering mechanisms in FeVSb half-Heusler thermoelectric von Shastri, Shivprasad S, Pandey, Sudhir K

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Abstract 2040: Influence of MDR1 and CYP3A5 genetic polymorphisms on trough levels and therapeutic response of imatinib in patients with chronic myeloid leukemia von Harivenkatesh, Natarajan, Kumar, Lalit, Bakhshi, Sameer, Sharma, Atul, Kabra, Madhulika, Velpandian, Thirumurthy, Gogia, Ajay, Shastri, Shivaram, Gupta, Yogendra Kumar

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Zinc Supplementation for One Year Among Children with Cystic Fibrosis Does Not Decrease Pulmonary Infection von Sharma, Ganesh, Lodha, Rakesh, Shastri, Shivaram, Saini, Savita, Kapil, Arti, Singla, Mohit, Mukherjee, Aparna, Jat, Kana Ram, Kabra, Madhulika, Kabra, Sushil K

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Aquagenic Wrinkling of Skin: A Screening Test for Cystic Fibrosis von Singh, Anuj, Lodha, Rakesh, Shastri, Shivaram, Sethuraman, G., Sreedevi, K. N., Kabra, Madhulika, Kabra, S. K.

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Identification of a novel homozygous mutation in transmembrane channel like 1 ( TMC1 ) gene, one of the second-tier hearing loss genes after GJB2 in India von Singh, Pawan Kumar, Ghosh, Manju, Sharma, Shipra, Shastri, Shivaram, Gupta, Neerja, Chowdhury, Madhumita Roy, Anand, Anuranjan, Kabra, Madhulika

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ADRB2 polymorphism and salbutamol responsiveness in Northern Indian children with mild to moderate exacerbation of asthma von Sahi, Puneet Kaur, Shastri, Shivaram, Lodha, Rakesh, Gupta, Neerja, Pandey, R. M., Kabra, Sushil Kumar, Kabra, Madhulika

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Prevalence of UGT1A6 polymorphisms in children with epilepsy on valproate monotherapy von Jain, Puneet, Shastri, Shivaram, Gulati, Sheffali, Kaleekal, Thomas, Kabra, Madhulika, Gupta, Neerja, Gupta, Y K, Pandey, Ravindra Mohan

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Norrie Disease: First Mutation Report and Prenatal Diagnosis in an Indian Family von Ghosh, Manju, Sharma, Shipra, Shastri, Shivaram, Arora, Sadhna, Shukla, Rashmi, Gupta, Neerja, Deka, Deepika, Kabra, Madhulika

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TMC1 may be a common gene for nonsyndromic hereditary hearing loss in Indian population von Singh, Pawan Kumar, Sharma, Shipra, Ghosh, Manju, Shastri, Shivaram S, Gupta, Neerja, Roy Chowdhury, Madhumita, Kabra, Madhulika

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Screening of families with autosomal recessive non-syndromic hearing impairment (ARNSHI) for mutations in GJB2 gene: Indian scenario von Maheshwari, Manjula, Vijaya, R., Ghosh, Manju, Shastri, Shivaram, Kabra, Madhulika, Menon, P.S.N.

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Glutaric Acidemia Type 1-Clinico-Molecular Profile and Novel Mutations in GCDH Gene in Indian Patients von Gupta, Neerja, Singh, Pawan Kumar, Kumar, Manoj, Shastri, Shivaram, Gulati, Sheffali, Kumar, Atin, Agarwala, Anuja, Kapoor, Seema, Nair, Mohandas, Sapra, Savita, Dubey, Sudhisha, Singh, Ankur, Kaur, Punit, Kabra, Madhulika

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Erratum to: Glutaric Acidemia Type 1-Clinico-Molecular Profile and Novel Mutations in GCDH Gene in Indian Patients von Gupta, Neerja, Singh, Pawan Kumar, Kumar, Manoj, Shastri, Shivaram, Gulati, Sheffali, Kumar, Atin, Agarwala, Anuja, Kapoor, Seema, Nair, Mohandas, Sapra, Savita, Dubey, Sudhisha, Singh, Ankur, Kaur, Punit, Kabra, Madhulika

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Prenatal diagnosis of Duchenne muscular dystrophy von Maheshwari, M, Vijaya, R, Kabra, M, Arora, S, Shastri, S S, Deka, D, Kriplani, A, Menon, P S

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