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Results: 1-8 |
Results: 8
SCA12 is a rare locus for autosomal dominant cerebellar ataxia: A study ofan Indian family
Authors: Fujigasaki, H Verma, IC Camuzat, A Margolis, RL Zander, C Lebre, AS Jamot, L Saxena, R Anand, I Holmes, SE Ross, CA Durr, A Brice, A
Citation: H. Fujigasaki et al., SCA12 is a rare locus for autosomal dominant cerebellar ataxia: A study ofan Indian family, ANN NEUROL, 49(1), 2001, pp. 117-121
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
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
Multicentric study of efficacy of periconceptional folic acid containing vitamin supplementation in prevention of open neural tube defects from India
Authors: Thomas, IM Hegde, S Agarwal, SS Sharma, S Phadke, S Pandey, CM Patel, ZM Adhia, R Verma, IC Jain, PK Ghosh, M Phadke, M Saxena, BN Arora, R Ahluwalia, TP
Citation: Im. Thomas et al., Multicentric study of efficacy of periconceptional folic acid containing vitamin supplementation in prevention of open neural tube defects from India, I J MED RES, 112, 2000, pp. 206-211
A beta-thalassaemia allele with 3 base substitution in codons 4/5 & 6 (ACTCCT GAG ACA TCT TAG) detected by denaturing gradient gel electrophoresis & sequencing
Authors: Saxena, R Moi, L Demurtas, M Rosatelli, MC Cao, A Verma, IC
Citation: R. Saxena et al., A beta-thalassaemia allele with 3 base substitution in codons 4/5 & 6 (ACTCCT GAG ACA TCT TAG) detected by denaturing gradient gel electrophoresis & sequencing, I J MED RES, 111, 2000, pp. 24-27
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
Hugo Ethics Committee statement on benefit sharing - April 9, 2000
Authors: Knoppers, BM Chadwick, R Takebe, H Berg, K Cantu, JM Daar, AS Engels, EM Kirby, M Macer, D Murray, TH Qui, RZ Wertz, DC Verma, IC
Citation: Bm. Knoppers et al., Hugo Ethics Committee statement on benefit sharing - April 9, 2000, CLIN GENET, 58(5), 2000, pp. 364-366
Risultati: 1-8 |