Aggarwal S - Search Results

1

Run-on mutation in the PAX6 gene and chorioretinal degeneration in autosomal dominant aniridia.

Aggarwal S, Jinda W, Limwongse C, Atchaneeyasakul LO, Phadke SR. Aggarwal S, et al. Mol Vis. 2011;17:1305-9. Epub 2011 May 7. Mol Vis. 2011. PMID: 21633710 Free PMC article.

2

Intracardiac echogenic focus and fetal outcome.

Gupta G, Aggarwal S, Phadke SR. Gupta G, et al. Among authors: aggarwal s. J Clin Ultrasound. 2010 Nov-Dec;38(9):466-9. doi: 10.1002/jcu.20741. J Clin Ultrasound. 2010. PMID: 20848571

3

Vascular endothelial growth factor gene polymorphisms in North Indian patients with recurrent miscarriages.

Aggarwal S, Parveen F, Faridi RM, Phadke S, Borkar M, Agrawal S. Aggarwal S, et al. Reprod Biomed Online. 2011 Jan;22(1):59-64. doi: 10.1016/j.rbmo.2010.08.005. Epub 2010 Aug 31. Reprod Biomed Online. 2011. PMID: 21126911

4

The expanding spectrum of Elejalde syndrome: overlap with other disorders of overgrowth.

Phadke SR, Aggarwal S, Kumari N. Phadke SR, et al. Among authors: aggarwal s. Clin Dysmorphol. 2011 Apr;20(2):98-101. doi: 10.1097/MCD.0b013e32833edace. Clin Dysmorphol. 2011. PMID: 21164339 No abstract available.

5

Late termination of pregnancy for fetal abnormalities: The perspective of Indian lay persons and medical practitioners.

Phadke SR, Agarwal M, Aggarwal S. Phadke SR, et al. Among authors: aggarwal s. Prenat Diagn. 2011 Dec;31(13):1286-91. doi: 10.1002/pd.2887. Epub 2011 Oct 26. Prenat Diagn. 2011. PMID: 22030841

6

Compound heterozygote condition in beta thalassemia major due to a novel single nucleotide deletion (-T) at codon 69 in association with IVS 1-5 (G>C) mutation.

Angalena R, Aggarwal S, Phadke SR, Dalal A. Angalena R, et al. Among authors: aggarwal s. Int J Lab Hematol. 2012 Aug;34(4):e7-9. doi: 10.1111/j.1751-553X.2012.01412.x. Epub 2012 Mar 12. Int J Lab Hematol. 2012. PMID: 22409273 No abstract available.

7

Aetiologic spectrum of mental retardation & developmental delay in India.

Aggarwal S, Bogula VR, Mandal K, Kumar R, Phadke SR. Aggarwal S, et al. Indian J Med Res. 2012 Sep;136(3):436-44. Indian J Med Res. 2012. PMID: 23041737 Free PMC article.

8

Recurrence of urorectal septum malformation sequence spectrum anomalies in siblings: time to explore the genetics.

Aggarwal S, Phadke SR. Aggarwal S, et al. Am J Med Genet A. 2013 Jul;161A(7):1718-21. doi: 10.1002/ajmg.a.35950. Epub 2013 May 17. Am J Med Genet A. 2013. PMID: 23686839

9

Prenatal diagnosis in India is not limited to sex selection.

Dalal AB, Ranganath P, Phadke SR, Kabra M, Danda S, Puri RD, Sankar VH, Gupta N, Patil SJ, Mandal K, Tamhankar P, Aggarwal S, Agarwal M. Dalal AB, et al. Among authors: aggarwal s. Genet Med. 2015 Jan;17(1):88. doi: 10.1038/gim.2014.149. Genet Med. 2015. PMID: 25356971 Free article. No abstract available.

10

Recurrent and novel GLB1 mutations in India.

Bidchol AM, Dalal A, Trivedi R, Shukla A, Nampoothiri S, Sankar VH, Danda S, Gupta N, Kabra M, Hebbar SA, Bhat RY, Matta D, Ekbote AV, Puri RD, Phadke SR, Gowrishankar K, Aggarwal S, Ranganath P, Sharda S, Kamate M, Datar CA, Bhat K, Kamath N, Shah H, Krishna S, Gopinath PM, Verma IC, Nagarajaram HA, Satyamoorthy K, Girisha KM. Bidchol AM, et al. Among authors: aggarwal s. Gene. 2015 Aug 10;567(2):173-81. doi: 10.1016/j.gene.2015.04.078. Epub 2015 Apr 30. Gene. 2015. PMID: 25936995

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