Lese CM[Author] - Search Results

Year	Number of Results
1995	1
1998	2
1999	2
2000	4
2001	2
2002	1
2022	0

1

Molecular cytogenetic analysis of telomere rearrangements.

Lese CM, Ledbetter DH. Lese CM, et al. Curr Protoc Hum Genet. 2001 May;Chapter 8:Unit 8.11. doi: 10.1002/0471142905.hg0811s24. Curr Protoc Hum Genet. 2001. PMID: 18428312 Review.

2

Prenatal diagnosis using interphase fluorescence in situ hybridization (FISH): 2-year multi-center retrospective study and review of the literature.

Tepperberg J, Pettenati MJ, Rao PN, Lese CM, Rita D, Wyandt H, Gersen S, White B, Schoonmaker MM. Tepperberg J, et al. Among authors: lese cm. Prenat Diagn. 2001 Apr;21(4):293-301. doi: 10.1002/pd.57. Prenat Diagn. 2001. PMID: 11288120 Review.

3

Visualization of INT2 and HST1 amplification in oral squamous cell carcinomas.

Lese CM, Rossie KM, Appel BN, Reddy JK, Johnson JT, Myers EN, Gollin SM. Lese CM, et al. Genes Chromosomes Cancer. 1995 Apr;12(4):288-95. doi: 10.1002/gcc.2870120409. Genes Chromosomes Cancer. 1995. PMID: 7539284

4

Partial paternal uniparental disomy of chromosome 6 in an infant with neonatal diabetes, macroglossia, and craniofacial abnormalities.

Das S, Lese CM, Song M, Jensen JL, Wells LA, Barnoski BL, Roseberry JA, Camacho JM, Ledbetter DH, Schnur RE. Das S, et al. Among authors: lese cm. Am J Hum Genet. 2000 Dec;67(6):1586-91. doi: 10.1086/316897. Epub 2000 Oct 18. Am J Hum Genet. 2000. PMID: 11038325 Free PMC article.

5

A consistent pattern of RIN1 rearrangements in oral squamous cell carcinoma cell lines supports a breakage-fusion-bridge cycle model for 11q13 amplification.

Shuster MI, Han L, Le Beau MM, Davis E, Sawicki M, Lese CM, Park NH, Colicelli J, Gollin SM. Shuster MI, et al. Among authors: lese cm. Genes Chromosomes Cancer. 2000 Jun;28(2):153-63. Genes Chromosomes Cancer. 2000. PMID: 10825000

6

Organisation of the pericentromeric region of chromosome 15: at least four partial gene copies are amplified in patients with a proximal duplication of 15q.

Fantes JA, Mewborn SK, Lese CM, Hedrick J, Brown RL, Dyomin V, Chaganti RS, Christian SL, Ledbetter DH. Fantes JA, et al. Among authors: lese cm. J Med Genet. 2002 Mar;39(3):170-7. doi: 10.1136/jmg.39.3.170. J Med Genet. 2002. PMID: 11897815 Free PMC article.

7

Medulloblastoma and glioblastoma multiforme in a patient with Turcot syndrome: a case report.

McLaughlin MR, Gollin SM, Lese CM, Albright AL. McLaughlin MR, et al. Among authors: lese cm. Surg Neurol. 1998 Mar;49(3):295-301. doi: 10.1016/s0090-3019(97)00214-0. Surg Neurol. 1998. PMID: 9508118

8

Satellited chromosome 10 detected prenatally in a fetus and confirmed as mosaic in a parent.

Storto PD, Diehn TN, O'Malley DP, Bullard BA, Netzloff ML, VanDyke DL, Feldman GL, Precht KS, Ledbetter DH, Lese CM. Storto PD, et al. Among authors: lese cm. Prenat Diagn. 1999 Nov;19(11):1088-9. doi: 10.1002/(sici)1097-0223(199911)19:11<1088::aid-pd692>3.0.co;2-r. Prenat Diagn. 1999. PMID: 10589072 No abstract available.

9

Usefulness and limitations of FISH to characterize partially cryptic complex chromosome rearrangements.

Kaiser-Rogers KA, Rao KW, Michaelis RC, Lese CM, Powell CM. Kaiser-Rogers KA, et al. Among authors: lese cm. Am J Med Genet. 2000 Nov 6;95(1):28-35. doi: 10.1002/1096-8628(20001106)95:1<28::aid-ajmg7>3.0.co;2-c. Am J Med Genet. 2000. PMID: 11074491

10

Characterization of physical gap sizes at human telomeres.

Lese CM, Fantes JA, Riethman HC, Ledbetter DH. Lese CM, et al. Genome Res. 1999 Sep;9(9):888-94. doi: 10.1101/gr.9.9.888. Genome Res. 1999. PMID: 10508848 Free PMC article.

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