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Results: 1-13 |
Results: 13
Diagnosis and management of congenital adrenal hyperplasia: Clinical, molecular and prenatal aspects
Authors: Mathur, R Kabra, M Menon, PSN
Citation: R. Mathur et al., Diagnosis and management of congenital adrenal hyperplasia: Clinical, molecular and prenatal aspects, NAT MED J I, 14(1), 2001, pp. 26-31
Factor IX gene polymorphisms in Indian population
Authors: Chowdhury, MR Kabra, M Menon, PSN
Citation: Mr. Chowdhury et al., Factor IX gene polymorphisms in Indian population, AM J HEMAT, 68(4), 2001, pp. 246-248
Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome
Authors: Liburd, N Ghosh, M Riazuddin, S Naz, S Khan, S Ahmed, Z Riazuddin, S Liang, Y Menon, PSN Smith, T Smith, ACM Chen, KS Lupski, JR Wilcox, ER Potocki, L Friedman, TB
Citation: N. Liburd et al., Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome, HUM GENET, 109(5), 2001, pp. 535-541
Autoimmune thyroid disease in Indian children with type 1 diabetes mellitus
Authors: Menon, PSN Vaidyanathan, B Kaur, M
Citation: Psn. Menon et al., Autoimmune thyroid disease in Indian children with type 1 diabetes mellitus, J PED END M, 14(3), 2001, pp. 279-286
Molecular characterization of mutations in Indian children with congenitaladrenal hyperplasia due to steroid 21-hydroxylase deficiency
Authors: Mathur, R Menon, PSN Kabra, M Goyal, RK Verma, IC
Citation: R. Mathur et al., Molecular characterization of mutations in Indian children with congenitaladrenal hyperplasia due to steroid 21-hydroxylase deficiency, J PED END M, 14(1), 2001, pp. 27-35
Detection of complex chromosomal rearrangements in a woman with repeated spontaneous abortions
Authors: Dubey, S Mathur, R Kabra, M Menon, PSN
Citation: S. Dubey et al., Detection of complex chromosomal rearrangements in a woman with repeated spontaneous abortions, ACT OBST SC, 80(5), 2001, pp. 478-479
Factor VIII gene polymorphisms in the Asian Indian population
Authors: Chowdhury, MR Herrmann, FH Schroder, W Lambert, CT Lalloz, MRA Layton, M Kumbnani, HK Kabra, M Menon, PSN Verma, IC
Citation: Mr. Chowdhury et al., Factor VIII gene polymorphisms in the Asian Indian population, HAEMOPHILIA, 6(6), 2000, pp. 625-630
Knowledge and attitudes of rural adolescent girls regarding reproductive health issues
Authors: Pattanaik, D Lobo, J Kapoor, SK Menon, PSN
Citation: D. Pattanaik et al., Knowledge and attitudes of rural adolescent girls regarding reproductive health issues, NAT MED J I, 13(3), 2000, pp. 124-128
Prenatal diagnosis of Duchenne muscular dystrophy
Authors: Maheshwari, M R, V Kabra, M Arora, S Shastri, SS Deka, D Kriplani, A Menon, PSN
Citation: M. Maheshwari et al., Prenatal diagnosis of Duchenne muscular dystrophy, NAT MED J I, 13(3), 2000, pp. 129-131
Is the spectrum of mutations in Indian patients with cystic fibrosis different?
Authors: Kabra, M Kabra, SK Ghosh, M Khanna, A Arora, S Menon, PSN Verma, IC Wallace, A
Citation: M. Kabra et al., Is the spectrum of mutations in Indian patients with cystic fibrosis different?, AM J MED G, 93(2), 2000, pp. 161-163
The challenge of haemoglobinopathies in India
Authors: Kabra, M Menon, PSN
Citation: M. Kabra et Psn. Menon, The challenge of haemoglobinopathies in India, NAT MED J I, 12(5), 1999, pp. 198-201
Use of growth hormone in non-growth hormone deficient children
Authors: Sood, A Menon, PSN
Citation: A. Sood et Psn. Menon, Use of growth hormone in non-growth hormone deficient children, NAT MED J I, 11(5), 1998, pp. 222-225
Hypothalamic hamartoma - Report of a case with unusual histologic features
Authors: Sharma, MC Gaikwad, S Mahapatra, AK Menon, PSN Sarkar, C
Citation: Mc. Sharma et al., Hypothalamic hamartoma - Report of a case with unusual histologic features, AM J SURG P, 22(12), 1998, pp. 1538-1541
Risultati: 1-13 |