Chowdhury MR - Search Results

1

A report of 5 Indian families with multicentric carpotarsal osteolysis syndrome.

Gupta N, Chakraborty S, Chowdhury MR, Puri RD, Jana M, Kumari I, Bhatia S, Kabra M. Gupta N, et al. Among authors: chowdhury mr. Eur J Med Genet. 2023 Sep;66(9):104822. doi: 10.1016/j.ejmg.2023.104822. Epub 2023 Aug 17. Eur J Med Genet. 2023. PMID: 37595943

2

Factor VIII gene polymorphisms in the Asian Indian population.

Chowdhury MR, Herrmann FH, Schroder W, Lambert CT, Lalloz MR, Layton M, Kumbnani HK, Kabra M, Menon PS, Verma IC. Chowdhury MR, et al. Haemophilia. 2000 Nov;6(6):625-30. doi: 10.1046/j.1365-2516.2000.00442.x. Haemophilia. 2000. PMID: 11122386

3

Factor IX gene polymorphisms in Indian population.

Chowdhury MR, Kabra M, Menon PS. Chowdhury MR, et al. Am J Hematol. 2001 Dec;68(4):246-8. doi: 10.1002/ajh.1189. Am J Hematol. 2001. PMID: 11754413 Free article.

4

Prenatal diagnosis in hemophilia A using factor VIII gene polymorphism--Indian experience.

Chowdhury MR, Tiwari M, Kabra M, Menon PS. Chowdhury MR, et al. Ann Hematol. 2003 Jul;82(7):427-30. doi: 10.1007/s00277-003-0670-9. Epub 2003 May 24. Ann Hematol. 2003. PMID: 12768323

5

Novel missense mutation in the coagulation factor IX catalytic domain associated with severe haemophilia B--Factor IXDelhi.

Mahajan A, Sharma A, Chavali S, Kabra M, Chowdhury MR, Srinivasan N, Bharadwaj D. Mahajan A, et al. Among authors: chowdhury mr. Haemophilia. 2004 Sep;10(5):550-2. doi: 10.1111/j.1365-2516.2004.00948.x. Haemophilia. 2004. PMID: 15357782

6

Molecular characterization of hemophilia B in North Indian families: identification of novel and recurrent molecular events in the factor IX gene.

Mahajan A, Chavali S, Kabra M, Chowdhury MR, Bharadwaj D. Mahajan A, et al. Among authors: chowdhury mr. Haematologica. 2004 Dec;89(12):1498-503. Haematologica. 2004. PMID: 15590401

7

Allelic heterogeneity of molecular events in human coagulation factor IX in Asian Indians. Mutation in brief #965. Online.

Mahajan A, Chavali S, Ghosh S, Kabra M, Chowdhury MR; Indian Genome Variation Consortium; Bharadwaj D. Mahajan A, et al. Among authors: chowdhury mr. Hum Mutat. 2007 May;28(5):526. doi: 10.1002/humu.9494. Hum Mutat. 2007. PMID: 17397055

8

Effectiveness and safety of donepezil in boys with fragile x syndrome: a double-blind, randomized, controlled pilot study.

Sahu JK, Gulati S, Sapra S, Arya R, Chauhan S, Chowdhury MR, Gupta N, Kabra M, Gupta YK, Dwivedi SN, Kalra V. Sahu JK, et al. Among authors: chowdhury mr. J Child Neurol. 2013 May;28(5):570-5. doi: 10.1177/0883073812449381. Epub 2012 Jun 29. J Child Neurol. 2013. PMID: 22752489 Clinical Trial.

9

Williams-Beuren Syndrome: Experience of 43 Patients and a Report of an Atypical Case from a Tertiary Care Center in India.

Sharma P, Gupta N, Chowdhury MR, Phadke SR, Sapra S, Halder A, Ghosh M, Kabra M. Sharma P, et al. Among authors: chowdhury mr. Cytogenet Genome Res. 2015;146(3):187-94. doi: 10.1159/000439205. Epub 2015 Sep 10. Cytogenet Genome Res. 2015. PMID: 26352091

10

Application of chromosomal microarrays in the evaluation of intellectual disability/global developmental delay patients - A study from a tertiary care genetic centre in India.

Sharma P, Gupta N, Chowdhury MR, Sapra S, Ghosh M, Gulati S, Kabra M. Sharma P, et al. Among authors: chowdhury mr. Gene. 2016 Sep 15;590(1):109-19. doi: 10.1016/j.gene.2016.06.020. Epub 2016 Jun 9. Gene. 2016. PMID: 27291820

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