Pandya A - Search Results

1

Cobblestone Malformation in LAMA2 Congenital Muscular Dystrophy (MDC1A).

Jayakody H, Zarei S, Nguyen H, Dalton J, Chen K, Hudgins L, Day J, Withrow K, Pandya A, Teasley J, Dobyns WB, Mathews KD, Moore SA. Jayakody H, et al. Among authors: pandya a. J Neuropathol Exp Neurol. 2020 Sep 1;79(9):998-1010. doi: 10.1093/jnen/nlaa062. J Neuropathol Exp Neurol. 2020. PMID: 32827036 Free PMC article.

2

Consumer motivations for pursuing genetic testing and their preferences for the provision of genetic services for hearing loss.

Withrow KA, Burton S, Arnos KS, Kalfoglou A, Pandya A. Withrow KA, et al. Among authors: pandya a. J Genet Couns. 2008 Jun;17(3):252-60. doi: 10.1007/s10897-007-9143-y. Epub 2008 Feb 5. J Genet Couns. 2008. PMID: 18247107

3

Impact of genetic advances and testing for hearing loss: results from a national consumer survey.

Withrow KA, Tracy KA, Burton SK, Norris VW, Maes HH, Arnos KS, Pandya A. Withrow KA, et al. Among authors: pandya a. Am J Med Genet A. 2009 Jun;149A(6):1159-68. doi: 10.1002/ajmg.a.32800. Am J Med Genet A. 2009. PMID: 19449400

4

Provision of genetic services for hearing loss: results from a national survey and comparison to insights obtained from previous focus group discussions.

Withrow KA, Tracy KA, Burton SK, Norris VW, Maes HH, Arnos KS, Pandya A. Withrow KA, et al. Among authors: pandya a. J Genet Couns. 2009 Dec;18(6):618-21. doi: 10.1007/s10897-009-9246-8. Epub 2009 Oct 2. J Genet Couns. 2009. PMID: 19798556

5

A focus group study of consumer attitudes toward genetic testing and newborn screening for deafness.

Burton SK, Withrow K, Arnos KS, Kalfoglou AL, Pandya A. Burton SK, et al. Among authors: pandya a. Genet Med. 2006 Dec;8(12):779-83. doi: 10.1097/01.gim.0000250501.59830.ff. Genet Med. 2006. PMID: 17172941 Free article.

6

Strategies and logistical requirements for efficient testing in genetic disease.

Jackson-Cook C, Pandya A. Jackson-Cook C, et al. Among authors: pandya a. Clin Lab Med. 1995 Dec;15(4):839-57. Clin Lab Med. 1995. PMID: 8838226 Review.

7

Intraventricular twin fetuses in fetu.

Huddle LN, Fuller C, Powell T, Hiemenga JA, Yan J, Deuell B, Lyders EM, Bodurtha JN, Papenhausen PR, Jackson-Cook CK, Pandya A, Jaworski M, Tye GW, Ritter AM. Huddle LN, et al. Among authors: pandya a. J Neurosurg Pediatr. 2012 Jan;9(1):17-23. doi: 10.3171/2011.10.PEDS11196. J Neurosurg Pediatr. 2012. PMID: 22208315

8

Chudley-McCullough syndrome: expanded phenotype and review of the literature.

Welch KO, Tekin M, Nance WE, Blanton SH, Arnos KS, Pandya A. Welch KO, et al. Among authors: pandya a. Am J Med Genet A. 2003 May 15;119A(1):71-6. doi: 10.1002/ajmg.a.10180. Am J Med Genet A. 2003. PMID: 12707963

9

Attitudes of deaf individuals towards genetic testing.

Taneja PR, Pandya A, Foley DL, Nicely LV, Arnos KS. Taneja PR, et al. Among authors: pandya a. Am J Med Genet A. 2004 Sep 15;130A(1):17-21. doi: 10.1002/ajmg.a.30051. Am J Med Genet A. 2004. PMID: 15368489

10

Education in the genetics of hearing loss: a survey of early hearing detection and intervention programs.

Burton SK, Blanton SH, Culpepper B, White KR, Pandya A, Nance WE, Arnos KS. Burton SK, et al. Among authors: pandya a. Genet Med. 2006 Aug;8(8):510-7. doi: 10.1097/01.gim.0000232462.55966.92. Genet Med. 2006. PMID: 16912582 Free article.

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