Jalal SM - Search Results

1

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.

2

Mosaic r(13) resulting in large deletion of chromosome 13q in a newborn female with multiple congenital anomalies.

Lorentz CP, Jalal SM, Thompson DM, Babovic-Vuksanovic D. Lorentz CP, et al. Among authors: jalal sm. Am J Med Genet. 2002 Jul 22;111(1):61-7. doi: 10.1002/ajmg.10457. Am J Med Genet. 2002. PMID: 12124737 Review.

3

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.

4

Nonmosaic smallest duplication of 12q24.31-qter: the first reported case.

Ireland JW, Jalal SM, McGrann PS, Lindor NM. Ireland JW, et al. Among authors: jalal sm. Am J Med Genet A. 2004 Jul 30;128A(3):305-10. doi: 10.1002/ajmg.a.30098. Am J Med Genet A. 2004. PMID: 15216553

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

Trisomy 20 mosaicism caused by a maternal meiosis II error is associated with normal intellect but multiple congenital anomalies.

Ensenauer RE, Shaughnessy WJ, Jalal SM, Dawson DB, Courteau LK, Ellison JW. Ensenauer RE, et al. Among authors: jalal sm. Am J Med Genet A. 2005 Apr 15;134A(2):202-6. doi: 10.1002/ajmg.a.30586. Am J Med Genet A. 2005. PMID: 15690403 Review.

7

Subtelomere deletions and translocations are frequently familial.

Adeyinka A, Adams SA, Lorentz CP, Van Dyke DL, Jalal SM. Adeyinka A, et al. Among authors: jalal sm. Am J Med Genet A. 2005 May 15;135(1):28-35. doi: 10.1002/ajmg.a.30675. Am J Med Genet A. 2005. PMID: 15810004

8

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

9

Delineation of the cryptic 1qter deletion phenotype.

Merritt JL 2nd, Zou Y, Jalal SM, Michels VV. Merritt JL 2nd, et al. Among authors: jalal sm. Am J Med Genet A. 2007 Mar 15;143A(6):599-603. doi: 10.1002/ajmg.a.31611. Am J Med Genet A. 2007. PMID: 17304549

10

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.

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