Sheth J - Search Results

1

Novel LINS1 missense mutation in a family with non-syndromic intellectual disability.

Sheth J, Ranjan G, Shah K, Bhavsar R, Sheth F. Sheth J, et al. Among authors: sheth f. Am J Med Genet A. 2017 Apr;173(4):1041-1046. doi: 10.1002/ajmg.a.38089. Epub 2017 Feb 9. Am J Med Genet A. 2017. PMID: 28181389

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. Among authors: sheth fj. 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. Among authors: sheth fj. 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. Among authors: sheth jj. 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

Genomewide scan for nonsyndromic cleft lip and palate in multigenerational Indian families reveals significant evidence of linkage at 13q33.1-34.

Radhakrishna U, Ratnamala U, Gaines M, Beiraghi S, Hutchings D, Golla J, Husain SA, Gambhir PS, Sheth JJ, Sheth FJ, Chetan GK, Naveed M, Solanki JV, Patel UC, Master DC, Memon R, Antonarakis GS, Antonarakis SE, Nath SK. Radhakrishna U, et al. Among authors: sheth jj, sheth fj. Am J Hum Genet. 2006 Sep;79(3):580-5. doi: 10.1086/507487. Epub 2006 Jul 21. Am J Hum Genet. 2006. PMID: 16909398 Free PMC article.

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