Sekhon GS - Search Results

1

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

2

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

3

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.

4

Waardenburg syndrome type I in a child with deletion (2) (q35q36.2).

Kirkpatrick SJ, Kent CM, Laxova R, Sekhon GS. Kirkpatrick SJ, et al. Among authors: sekhon gs. Am J Med Genet. 1992 Nov 15;44(5):699-700. doi: 10.1002/ajmg.1320440533. Am J Med Genet. 1992. PMID: 1481835 Review. No abstract available.

5

Terminal deletion of 6q and Fryns syndrome: a microdeletion/syndrome pair?

Krassikoff N, Sekhon GS. Krassikoff N, et al. Among authors: sekhon gs. Am J Med Genet. 1990 Jul;36(3):363-4. doi: 10.1002/ajmg.1320360327. Am J Med Genet. 1990. PMID: 2363440 No abstract available.

6

De novo translocation involving chromosomes 1 and 4 resulting in partial duplication of 4q and partial deletion of 1p.

Legare JM, Sekhon GS, Laxova R. Legare JM, et al. Among authors: sekhon gs. Am J Med Genet. 1994 Nov 15;53(3):216-21. doi: 10.1002/ajmg.1320530304. Am J Med Genet. 1994. PMID: 7856655 Review.

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. 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.

8

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.

9

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.

10

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

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