Kabra M - 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: kabra m. 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. Among authors: kabra m. 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. Among authors: kabra m. 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. Among authors: kabra m. 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: kabra m. 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: kabra m. Haematologica. 2004 Dec;89(12):1498-503. Haematologica. 2004. PMID: 15590401

7

A female with hemihypertrophy and chylous ascites - Klippel-Trenaunay syndrome or Proteus syndrome: a diagnostic dilemma.

Gupta N, Kabra M, Ramesh K, Garg G, Kaur D, Gupta A, Bal CS. Gupta N, et al. Among authors: kabra m. Clin Dysmorphol. 2006 Oct;15(4):229-231. doi: 10.1097/01.mcd.0000228420.82037.51. Clin Dysmorphol. 2006. PMID: 16957479

8

Prenatal diagnosis for a novel homozygous mutation in PKLR gene in an Indian family.

Gupta N, Bianchi P, Fermo E, Kabra M, Warang P, Kedar P, Gupta N, Colah R. Gupta N, et al. Among authors: kabra m. Prenat Diagn. 2007 Feb;27(2):117-8. doi: 10.1002/pd.1616. Prenat Diagn. 2007. PMID: 17191259

9

Maffucci syndrome.

Gupta N, Kabra M. Gupta N, et al. Among authors: kabra m. Indian Pediatr. 2007 Feb;44(2):149-50. Indian Pediatr. 2007. PMID: 17351310 Free article. No abstract available.

10

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: kabra m. Hum Mutat. 2007 May;28(5):526. doi: 10.1002/humu.9494. Hum Mutat. 2007. PMID: 17397055

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