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Results: 1-9 |
Results: 9
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
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
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? (vol 93, pg 161, 2000)
Authors: Kabra, M Kabra, SK Ghosh, M Khanna, A Arora, S Menon, PS Verma, IC Wallace, A
Citation: M. Kabra et al., Is the spectrum of mutations in Indian patients with cystic fibrosis different? (vol 93, pg 161, 2000), AM J MED G, 95(4), 2000, pp. 410-410
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
Risultati: 1-9 |