Richer CL - Search Results

1

Characterization by fluorescence and electron microscopy in situ hybridization of a double Y isochromosome.

Fetni R, Krabchi K, Messier PE, Richer CL, Lemieux N. Fetni R, et al. Among authors: richer cl. Am J Med Genet. 1996 Jun 14;63(3):454-7. doi: 10.1002/(SICI)1096-8628(19960614)63:3<454::AID-AJMG7>3.0.CO;2-R. Am J Med Genet. 1996. PMID: 8737651

2

Detection of small, single-copy genes on protein-G-banded chromosomes by electron microscopy.

Fetni R, Lemieux N, Malfoy B, Dutrillaux B, Messier PE, Richer CL. Fetni R, et al. Among authors: richer cl. Cytogenet Cell Genet. 1992;60(3-4):187-9. doi: 10.1159/000133332. Cytogenet Cell Genet. 1992. PMID: 1505213

3

Simultaneous visualization of chromosome bands and hybridization signal using colloidal-gold labeling in electron microscopy.

Fetni R, Drouin R, Lemieux N, Messier PE, Richer CL. Fetni R, et al. Among authors: richer cl. Proc Natl Acad Sci U S A. 1991 Dec 1;88(23):10916-20. doi: 10.1073/pnas.88.23.10916. Proc Natl Acad Sci U S A. 1991. PMID: 1961763 Free PMC article.

4

Chromosome evolution and high-resolution analysis of leucocytes, bone marrow, and tumor cells of retinoblastoma patients.

Lemieux N, Richer CL. Lemieux N, et al. Among authors: richer cl. Am J Med Genet. 1990 Aug;36(4):456-62. doi: 10.1002/ajmg.1320360417. Am J Med Genet. 1990. PMID: 2389803

5

Detection by electron microscopy of a small subband 13q14.11 deletion in an hereditary retinoblastoma.

Lemieux N, Messier PE, Drouin R, Jacob JL, Milot J, Richer CL. Lemieux N, et al. Among authors: richer cl. Cancer Genet Cytogenet. 1990 Sep;48(2):265-9. doi: 10.1016/0165-4608(90)90130-3. Cancer Genet Cytogenet. 1990. PMID: 2397457

6

A man with isochromosome Xq Klinefelter syndrome with lack of height increase and normal androgenization.

Richer CL, Bleau G, Chapdelaine A, Murer-Orlando M, Lemieux N, Cadotte M. Richer CL, et al. Am J Med Genet. 1989 Jan;32(1):42-4. doi: 10.1002/ajmg.1320320110. Am J Med Genet. 1989. PMID: 2705482

7

Dynamic G- and R-banding of human chromosomes for electron microscopy.

Drouin R, Messier PE, Richer CL. Drouin R, et al. Among authors: richer cl. Chromosoma. 1989 Jun;98(1):40-8. doi: 10.1007/BF00293333. Chromosoma. 1989. PMID: 2766879

8

Electron microscopy of gold-labeled human and equine chromosomes.

Messier PE, Drouin R, Richer CL. Messier PE, et al. Among authors: richer cl. J Histochem Cytochem. 1989 Sep;37(9):1443-7. doi: 10.1177/37.9.2768813. J Histochem Cytochem. 1989. PMID: 2768813

9

Human chromosome banding specific for electron microscopy.

Drouin R, Messier PE, Richer CL. Drouin R, et al. Among authors: richer cl. Cytogenet Cell Genet. 1988;47(3):117-20. doi: 10.1159/000132526. Cytogenet Cell Genet. 1988. PMID: 3378449

10

Fragile site and interstitial telomere repeat sequences at the fusion point of a de novo (Y;13) translocation.

Boutouil M, Fetni R, Qu J, Dallaire L, Richer CL, Lemieux N. Boutouil M, et al. Among authors: richer cl. Hum Genet. 1996 Sep;98(3):323-7. doi: 10.1007/s004390050216. Hum Genet. 1996. PMID: 8707303

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