Jalal SM - Search Results

1

Molecular diagnosis of Ewing's sarcoma/primitive neuroectodermal tumor in formalin-fixed paraffin-embedded tissues by RT-PCR and fluorescence in situ hybridization.

Qian X, Jin L, Shearer BM, Ketterling RP, Jalal SM, Lloyd RV. Qian X, et al. Among authors: jalal sm. Diagn Mol Pathol. 2005 Mar;14(1):23-8. doi: 10.1097/01.pdm.0000140192.27878.97. Diagn Mol Pathol. 2005. PMID: 15714060

2

Analysis of parathyroid neoplasms by interphase fluorescence in situ hybridization.

Erickson LA, Jalal SM, Harwood A, Shearer B, Jin L, Lloyd RV. Erickson LA, et al. Among authors: jalal sm. Am J Surg Pathol. 2004 May;28(5):578-84. doi: 10.1097/00000478-200405000-00003. Am J Surg Pathol. 2004. PMID: 15105644

3

Analysis of Hurthle cell neoplasms of the thyroid by interphase fluorescence in situ hybridization.

Erickson LA, Jalal SM, Goellner JR, Law ME, Harwood A, Jin L, Roche PC, Lloyd RV. Erickson LA, et al. Among authors: jalal sm. Am J Surg Pathol. 2001 Jul;25(7):911-7. doi: 10.1097/00000478-200107000-00009. Am J Surg Pathol. 2001. PMID: 11420462

4

Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients.

Ensenauer RE, Adeyinka A, Flynn HC, Michels VV, Lindor NM, Dawson DB, Thorland EC, Lorentz CP, Goldstein JL, McDonald MT, Smith WE, Simon-Fayard E, Alexander AA, Kulharya AS, Ketterling RP, Clark RD, Jalal SM. Ensenauer RE, et al. Among authors: jalal sm. Am J Hum Genet. 2003 Nov;73(5):1027-40. doi: 10.1086/378818. Epub 2003 Oct 2. Am J Hum Genet. 2003. PMID: 14526392 Free PMC article.

5

Familial 22q11.2 deletions in DiGeorge/velocardiofacial syndrome are predominantly smaller than the commonly observed 3Mb.

Adeyinka A, Stockero KJ, Flynn HC, Lorentz CP, Ketterling RP, Jalal SM. Adeyinka A, et al. Among authors: jalal sm. Genet Med. 2004 Nov-Dec;6(6):517-20. doi: 10.1097/01.gim.0000144011.97407.b6. Genet Med. 2004. PMID: 15545748

6

Reflex fluorescent in situ hybridization testing for unsuccessful product of conception cultures: a retrospective analysis of 5555 samples attempted by conventional cytogenetics and fluorescent in situ hybridization.

Shearer BM, Thorland EC, Carlson AW, Jalal SM, Ketterling RP. Shearer BM, et al. Among authors: jalal sm. Genet Med. 2011 Jun;13(6):545-52. doi: 10.1097/GIM.0b013e31820c685b. Genet Med. 2011. PMID: 21415758 Free article.

7

Utility of subtelomeric fluorescent DNA probes for detection of chromosome anomalies in 425 patients.

Jalal SM, Harwood AR, Sekhon GS, Pham Lorentz C, Ketterling RP, Babovic-Vuksanovic D, Meyer RG, Ensenauer R, Anderson MH Jr, Michels VV. Jalal SM, et al. Genet Med. 2003 Jan-Feb;5(1):28-34. doi: 10.1097/00125817-200301000-00005. Genet Med. 2003. PMID: 12544473 Free article.

8

Detection of t(2;5) in anaplastic large cell lymphoma: comparison of immunohistochemical studies, FISH, and RT-PCR in paraffin-embedded tissue.

Cataldo KA, Jalal SM, Law ME, Ansell SM, Inwards DJ, Fine M, Arber DA, Pulford KA, Strickler JG. Cataldo KA, et al. Among authors: jalal sm. Am J Surg Pathol. 1999 Nov;23(11):1386-92. doi: 10.1097/00000478-199911000-00009. Am J Surg Pathol. 1999. PMID: 10555007 Clinical Trial.

9

Inherited interstitial deletion of chromosomes 5p and 16q without apparent phenotypic effect: further confirmation.

Hand JL, Michels VV, Marinello MJ, Ketterling RP, Jalal SM. Hand JL, et al. Among authors: jalal sm. Prenat Diagn. 2000 Feb;20(2):144-8; discussion 149-51. doi: 10.1002/(sici)1097-0223(200002)20:2<144::aid-pd770>3.0.co;2-9. Prenat Diagn. 2000. PMID: 10694687

10

Detection of newborn aneuploidy by interphase fluorescence in situ hybridization.

Jalal SM, Law ME. Jalal SM, et al. Mayo Clin Proc. 1997 Aug;72(8):705-10. doi: 10.4065/72.8.705. Mayo Clin Proc. 1997. PMID: 9276596

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