Kabra M - Search Results

1

Nasopharyngeal teratoma, congenital diaphragmatic hernia and Dandy-Walker malformation - a yet uncharacterized syndrome.

Gupta N, Shastri S, Singh PK, Jana M, Mridha A, Verma G, Kabra M. Gupta N, et al. Among authors: kabra m. Clin Genet. 2016 Nov;90(5):470-471. doi: 10.1111/cge.12830. Epub 2016 Aug 10. Clin Genet. 2016. PMID: 27506516

2

Prenatal diagnosis of Duchenne muscular dystrophy.

Maheshwari M, Vijaya R, Kabra M, Arora S, Shastri SS, Deka D, Kriplani A, Menon PS. Maheshwari M, et al. Among authors: kabra m. Natl Med J India. 2000 May-Jun;13(3):129-31. Natl Med J India. 2000. PMID: 11558111

3

Prenatal diagnosis of haemoglobinopathies.

Arora S, Kabra M, Maheshwari M, Shastri S, Kaur D, Deka D, Kriplani A, Menon PS. Arora S, et al. Among authors: kabra m. Natl Med J India. 2001 Nov-Dec;14(6):340-2. Natl Med J India. 2001. PMID: 11804364

4

An indigenously developed method for sweat collection and estimation of chloride for diagnosis of cystic fibrosis.

Kabra SK, Kabra M, Gera S, Lodha R, Sreedevi KN, Chacko S, Mathew J, Shastri S, Ghosh M. Kabra SK, et al. Among authors: kabra m. Indian Pediatr. 2002 Nov;39(11):1039-43. Indian Pediatr. 2002. PMID: 12466575

5

Screening of families with autosomal recessive non-syndromic hearing impairment (ARNSHI) for mutations in GJB2 gene: Indian scenario.

Maheshwari M, Vijaya R, Ghosh M, Shastri S, Kabra M, Menon PS. Maheshwari M, et al. Among authors: kabra m. Am J Med Genet A. 2003 Jul 15;120A(2):180-4. doi: 10.1002/ajmg.a.20014. Am J Med Genet A. 2003. PMID: 12833397

6

Clinical profile and frequency of delta f508 mutation in Indian children with cystic fibrosis.

Kabra SK, Kabra M, Lodha R, Shastri S, Ghosh M, Pandey RM, Kapil A, Aggarwal G, Kapoor V. Kabra SK, et al. Among authors: kabra m. Indian Pediatr. 2003 Jul;40(7):612-9. Indian Pediatr. 2003. PMID: 12881616 Free article.

7

Prevalence of the triple X syndrome in phenotypically normal women with premature ovarian failure and its association with autoimmune thyroid disorders.

Goswami R, Goswami D, Kabra M, Gupta N, Dubey S, Dadhwal V. Goswami R, et al. Among authors: kabra m. Fertil Steril. 2003 Oct;80(4):1052-4. doi: 10.1016/s0015-0282(03)01121-x. Fertil Steril. 2003. PMID: 14556833 Free article.

8

Carrier frequency of F508del mutation of cystic fibrosis in Indian population.

Kapoor V, Shastri SS, Kabra M, Kabra SK, Ramachandran V, Arora S, Balakrishnan P, Deorari AK, Paul VK. Kapoor V, et al. Among authors: kabra m, kabra sk. J Cyst Fibros. 2006 Jan;5(1):43-6. doi: 10.1016/j.jcf.2005.10.002. Epub 2005 Nov 28. J Cyst Fibros. 2006. PMID: 16311077 Free article.

9

Diagnosing and managing cystic fibrosis in the developing world.

Kabra SK, Kabra M, Shastri S, Lodha R. Kabra SK, et al. Among authors: kabra m. Paediatr Respir Rev. 2006;7 Suppl 1:S147-50. doi: 10.1016/j.prrv.2006.04.218. Epub 2006 Jun 6. Paediatr Respir Rev. 2006. PMID: 16798545 Review.

10

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

412 results

Search Page

Filters