Lall M - Search Results

1

A 54 Mb 11qter duplication and 0.9 Mb 1q44 deletion in a child with laryngomalacia and agenesis of corpus callosum.

Lall M, Thakur S, Puri R, Verma I, Mukerji M, Jha P. Lall M, et al. Mol Cytogenet. 2011 Sep 21;4:19. doi: 10.1186/1755-8166-4-19. Mol Cytogenet. 2011. PMID: 21936942 Free PMC article.

2

Genetic counseling and prenatal diagnosis in India--experience at Sir Ganga Ram Hospital.

Verma IC, Saxena R, Lall M, Bijarnia S, Sharma R. Verma IC, et al. Among authors: lall m. Indian J Pediatr. 2003 Apr;70(4):293-7. doi: 10.1007/BF02723582. Indian J Pediatr. 2003. PMID: 12793304

3

Down syndrome in India--diagnosis, screening, and prenatal diagnosis.

Verma IC, Lall M, Dua Puri R. Verma IC, et al. Among authors: lall m. Clin Lab Med. 2012 Jun;32(2):231-48. doi: 10.1016/j.cll.2012.04.010. Clin Lab Med. 2012. PMID: 22727002 Review.

4

A familial deletion 4q syndrome: An outcome of a paracentric inversion.

Lall M, Puri R, Saviour P, Verma I. Lall M, et al. Indian J Hum Genet. 2012 May;18(2):238-40. doi: 10.4103/0971-6866.100780. Indian J Hum Genet. 2012. PMID: 23162304 Free PMC article.

5

Is the diagnostic yield influenced by the indication for fetal autopsy?

Puri RD, Kotecha U, Lall M, Dash P, Bijarnia-Mahay S, Verma IC. Puri RD, et al. Among authors: lall m. Am J Med Genet A. 2016 Aug;170(8):2119-26. doi: 10.1002/ajmg.a.37743. Epub 2016 May 20. Am J Med Genet A. 2016. PMID: 27197608

6

Preimplantation genetic screening for all 24 chromosomes by microarray comparative genomic hybridization significantly increases implantation rates and clinical pregnancy rates in patients undergoing in vitro fertilization with poor prognosis.

Majumdar G, Majumdar A, Lall M, Verma IC, Upadhyaya KC. Majumdar G, et al. Among authors: lall m. J Hum Reprod Sci. 2016 Apr-Jun;9(2):94-100. doi: 10.4103/0974-1208.183512. J Hum Reprod Sci. 2016. PMID: 27382234 Free PMC article.

7

The HLA-G 14 bp insertion/deletion polymorphism and its association with soluble HLA-G levels in women with recurrent miscarriages.

Kalotra V, Lall M, Verma IC, Kaur A, Kaur A. Kalotra V, et al. Among authors: lall m. HLA. 2018 Mar;91(3):167-174. doi: 10.1111/tan.13198. HLA. 2018. PMID: 29280596

8

Prevalence of Cytogenetic Anomalies in Couples with Recurrent Miscarriages: A Case-control Study.

Kalotra V, Lall M, Saviour P, Verma IC, Kaur A. Kalotra V, et al. Among authors: lall m. J Hum Reprod Sci. 2017 Oct-Dec;10(4):302-309. doi: 10.4103/jhrs.JHRS_68_17. J Hum Reprod Sci. 2017. PMID: 29430159 Free PMC article.

9

Noninvasive prenatal testing (NIPT) detects variant of Turner syndrome not detectable by fluorescent in situ hybridization.

Eswarachari V, Kadam P, Movva S, Lingaiah S, Akther RM, Kidangan FX, Gowda KC, Golakoti RRK, Lall M, Mahajan S, Saviour P, Puri R, Verma IC, Vedam RL. Eswarachari V, et al. Among authors: lall m. J Matern Fetal Neonatal Med. 2019 Dec;32(24):4177-4180. doi: 10.1080/14767058.2018.1481383. Epub 2018 Jun 13. J Matern Fetal Neonatal Med. 2019. PMID: 29793366

10

Extending the Phenotype and Identification of a Novel Candidate Gene for Immunodeficiency in 5q11 Microdeletion Syndrome.

Arora V, Aggarwal S, Bijarnia S, Lall M, Joshi A, Dua-Puri R, Arora U, Verma I. Arora V, et al. Among authors: lall m. Mol Syndromol. 2019 Jan;9(6):312-318. doi: 10.1159/000494995. Epub 2018 Dec 14. Mol Syndromol. 2019. PMID: 30800048 Free PMC article.

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