Jalal S - Search Results

1

Human SULT1A3 pharmacogenetics: gene duplication and functional genomic studies.

Hildebrandt MA, Salavaggione OE, Martin YN, Flynn HC, Jalal S, Wieben ED, Weinshilboum RM. Hildebrandt MA, et al. Among authors: jalal s. Biochem Biophys Res Commun. 2004 Sep 3;321(4):870-8. doi: 10.1016/j.bbrc.2004.07.038. Biochem Biophys Res Commun. 2004. PMID: 15358107

2

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.

3

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. Genet Med. 2004 Nov-Dec;6(6):517-20. doi: 10.1097/01.gim.0000144011.97407.b6. Genet Med. 2004. PMID: 15545748

4

Characteristics of two cases with dup(15)(q11.2-q12): one of maternal and one of paternal origin.

Mao R, Jalal SM, Snow K, Michels VV, Szabo SM, Babovic-Vuksanovic D. Mao R, et al. Among authors: jalal sm. Genet Med. 2000 Mar-Apr;2(2):131-5. doi: 10.1097/00125817-200003000-00003. Genet Med. 2000. PMID: 11397326 Free article. Review.

5

Chromosomal abnormalities in systemic amyloidosis.

Fonseca R, Ahmann GJ, Jalal SM, Dewald GW, Larson DR, Therneau TM, Gertz MA, Kyle RA, Greipp PR. Fonseca R, et al. Among authors: jalal sm. Br J Haematol. 1998 Dec;103(3):704-10. doi: 10.1046/j.1365-2141.1998.01034.x. Br J Haematol. 1998. PMID: 9858220 Free article.

6

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.

7

Unbalanced cryptic 5p deletion/17p duplication identified by subtelomeric FISH in a family with a boy with chimerism and a balanced t(4;5).

Ensenauer R, Jalal S, Meyer R, Babovic-Vuksanovic D. Ensenauer R, et al. Among authors: jalal s. Am J Med Genet A. 2004 Feb 15;125A(1):86-91. doi: 10.1002/ajmg.a.20420. Am J Med Genet A. 2004. PMID: 14755472

8

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

9

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. Diagn Mol Pathol. 2005 Mar;14(1):23-8. doi: 10.1097/01.pdm.0000140192.27878.97. Diagn Mol Pathol. 2005. PMID: 15714060

10

Mosaic ring 20 with no detectable deletion by FISH analysis: Characteristic seizure disorder and literature review.

Zou YS, Van Dyke DL, Thorland EC, Chhabra HS, Michels VV, Keefe JG, Lega MA, Feely MA, Uphoff TS, Jalal SM. Zou YS, et al. Among authors: jalal sm. Am J Med Genet A. 2006 Aug 1;140(15):1696-706. doi: 10.1002/ajmg.a.31332. Am J Med Genet A. 2006. PMID: 16835934

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