Sekhon GS - Search Results

1

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. Among authors: sekhon gs. Genet Med. 2003 Jan-Feb;5(1):28-34. doi: 10.1097/00125817-200301000-00005. Genet Med. 2003. PMID: 12544473 Free article.

2

Application of multicolor fluorescent in situ hybridization for enhanced characterization of chromosomal abnormalities in congenital disorders.

Jalal SM, Law ME, Lindor NM, Thompson KJ, Sekhon GS. Jalal SM, et al. Among authors: sekhon gs. Mayo Clin Proc. 2001 Jan;76(1):16-21. doi: 10.4065/76.1.16. Mayo Clin Proc. 2001. PMID: 11155407

3

Interstitial deletion of (17)(p11.2p11.2): report of six additional patients with a new chromosome deletion syndrome.

Stratton RF, Dobyns WB, Greenberg F, DeSana JB, Moore C, Fidone G, Runge GH, Feldman P, Sekhon GS, Pauli RM, et al. Stratton RF, et al. Among authors: sekhon gs. Am J Med Genet. 1986 Jul;24(3):421-32. doi: 10.1002/ajmg.1320240305. Am J Med Genet. 1986. PMID: 3728561

4

Prenatal detection of 46,XY,rec(5),dup q, inv(5)(p13q33) using DNA analysis, flow cytometry, and in situ hybridization to supplement classical cytogenetic analysis.

Martin AO, Northrup H, Ledbetter DH, Trask B, van den Engh G, Le Beau MM, Beaudet AL, Gray JW, Sekhon G, Krassikoff N, et al. Martin AO, et al. Am J Med Genet. 1988 Nov;31(3):643-54. doi: 10.1002/ajmg.1320310320. Am J Med Genet. 1988. PMID: 3228143

5

Ventricular noncompaction and distal chromosome 5q deletion.

Pauli RM, Scheib-Wixted S, Cripe L, Izumo S, Sekhon GS. Pauli RM, et al. Among authors: sekhon gs. Am J Med Genet. 1999 Aug 6;85(4):419-23. Am J Med Genet. 1999. PMID: 10398271

6

A new syndrome of proximal deletion of the long arm of chromosome 1: 1q21-23 leads to 1q25.

Taysi K, Sekhon GS, Hillman RE. Taysi K, et al. Among authors: sekhon gs. Am J Med Genet. 1982 Dec;13(4):423-30. doi: 10.1002/ajmg.1320130411. Am J Med Genet. 1982. PMID: 7158642 No abstract available.

7

Pathological case of the month. Chromosome 10 qter deletion syndrome.

Costakos DT, Love LA, Josephson K, Sekhon G. Costakos DT, et al. Arch Pediatr Adolesc Med. 1998 May;152(5):507-8. doi: 10.1001/archpedi.152.5.507. Arch Pediatr Adolesc Med. 1998. PMID: 9605038 No abstract available.

8

Mosaic isochromosome 12p.

Pauli RM, Zeier RA, Sekhon GS. Pauli RM, et al. Among authors: sekhon gs. Am J Med Genet. 1987 Jun;27(2):291-4. doi: 10.1002/ajmg.1320270207. Am J Med Genet. 1987. PMID: 3605215 No abstract available.

9

Recent experience in prenatal fra(X) detection.

Jenkins EC, Brown WT, Krawczun MS, Duncan CJ, Lele KP, Cantu ES, Schonberg S, Golbus MS, Sekhon GS, Stark S, et al. Jenkins EC, et al. Among authors: sekhon gs. Am J Med Genet. 1988 May-Jun;30(1-2):329-36. doi: 10.1002/ajmg.1320300133. Am J Med Genet. 1988. PMID: 2972205

10

Detection of mosaicism in amniotic fluid cultures: a CYTO2000 collaborative study.

Ing PS, Van Dyke DL, Caudill SP, Reidy JA, Bice G, Bieber FR, Buchanan PD, Carroll AJ, Cheung SW, DeWald G, Donahue RP, Gardner HA, Higgins J, Hsu LY, Jamehdor M, Keitges EA, Laundon CH, Luthardt FW, Mascarello J, May KM, Meck JM, Morton C, Patil S, Peakman D, Pettenati MJ, Rao N, Sanger WG, Saxe DF, Schwartz S, Sekhon GS, Vance GH, Wyandt HE, Yu CW, Zenger-Hain J, Chen AT. Ing PS, et al. Among authors: sekhon gs. Genet Med. 1999 Mar-Apr;1(3):94-7. doi: 10.1097/00125817-199903000-00006. Genet Med. 1999. PMID: 11336459 Free article.

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