Sheth F - Search Results

1

Expanding the spectrum of HEXA mutations in Indian patients with Tay-Sachs disease.

Sheth J, Mistri M, Datar C, Kalane U, Patil S, Kamate M, Shah H, Nampoothiri S, Gupta S, Sheth F. Sheth J, et al. Among authors: sheth f. Mol Genet Metab Rep. 2014 Sep 29;1:425-430. doi: 10.1016/j.ymgmr.2014.09.004. eCollection 2014. Mol Genet Metab Rep. 2014. PMID: 27896118 Free PMC article.

2

Incomplete gonadal dysgenesis.

Sheth FJ, Multani AS, Sheth JJ, Radhakrishna U, Shah VC, Chinoy NJ. Sheth FJ, et al. Among authors: sheth jj. Urol Int. 1996;56(1):57-60. doi: 10.1159/000282812. Urol Int. 1996. PMID: 8903559

3

The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region.

Radhakrishna U, Blouin JL, Mehenni H, Mehta TY, Sheth FJ, Sheth JJ, Solanki JV, Antonarakis SE. Radhakrishna U, et al. Among authors: sheth jj, sheth fj. Am J Med Genet. 1997 Jul 11;71(1):80-6. doi: 10.1002/(sici)1096-8628(19970711)71:1<80::aid-ajmg15>3.0.co;2-r. Am J Med Genet. 1997. PMID: 9215774

4

Morquio-B syndrome (MPS-IV B) associated with beta-galactosidase deficiency in two siblings.

Sheth JJ, Sheth FJ, Bhattacharya R. Sheth JJ, et al. Indian J Pediatr. 2002 Jan;69(1):109-11. doi: 10.1007/BF02723790. Indian J Pediatr. 2002. PMID: 11876111

5

Study of anticardiolipin antibodies in repeated abortions--an institutional experience.

Sheth JJ, Sheth FJ. Sheth JJ, et al. Among authors: sheth fj. Indian J Pathol Microbiol. 2001 Apr;44(2):117-21. Indian J Pathol Microbiol. 2001. PMID: 11883124

6

Prenatal diagnosis of tay-sachs b1 variant in a maharashtrian family.

Sheth J, Bhattacharya R, Sheth F. Sheth J, et al. Among authors: sheth f. Indian Pediatr. 2002 Jul;39(7):704-6. Indian Pediatr. 2002. PMID: 12147910 No abstract available.

7

Gene polymorphism and folate metabolism: a maternal risk factor for Down syndrome.

Sheth JJ, Sheth FJ. Sheth JJ, et al. Indian Pediatr. 2003 Feb;40(2):115-23. Indian Pediatr. 2003. PMID: 12626825

8

Lysosomal storage disorders.

Sheth J, Patel P, Sheth F, Shah R. Sheth J, et al. Among authors: sheth f. Indian Pediatr. 2004 Mar;41(3):260-5. Indian Pediatr. 2004. PMID: 15064514 Free article.

9

Case of near triploidy with i(17)(q10) in blast crisis CML.

Sheth FJ, Sheth JJ, Desai C. Sheth FJ, et al. Cancer Genet Cytogenet. 2006 Jan 15;164(2):177-8. doi: 10.1016/j.cancergencyto.2005.07.022. Cancer Genet Cytogenet. 2006. PMID: 16434327 No abstract available.

10

Ring chromosome 9 in a dysmorphic child.

Sheth J, Joshi R, Sheth F. Sheth J, et al. Among authors: sheth f. Indian J Pediatr. 2007 May;74(5):507-8. doi: 10.1007/s12098-007-0090-2. Indian J Pediatr. 2007. PMID: 17526969

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