Cacheux V - Search Results

1

Analysis of uncultured amniocytes by comparative genomic hybridization: a prospective prenatal study.

Lapierre JM, Cacheux V, Luton D, Collot N, Oury JF, Aurias A, Tachdjian G. Lapierre JM, et al. Among authors: cacheux v. Prenat Diagn. 2000 Feb;20(2):123-31. doi: 10.1002/(sici)1097-0223(200002)20:2<123::aid-pd762>3.0.co;2-b. Prenat Diagn. 2000. PMID: 10694684

2

Evaluation of X, Y, 18, and 13/21 alpha satellite DNA probes for interphase cytogenetic analysis of uncultured amniocytes by fluorescence in situ hybridization.

Cacheux V, Tachdjian G, Druart L, Oury JF, Sérero S, Blot P, Nessmann C. Cacheux V, et al. Prenat Diagn. 1994 Feb;14(2):79-86. doi: 10.1002/pd.1970140202. Prenat Diagn. 1994. PMID: 8183853

3

Prenatal diagnosis of a (X;X) translocation by fluorescence in situ hybridization and laser scanning image cytometry.

Tachdjian G, Cacheux V, Kiefer H, Druart L, Lapierre JM, Oury JF, Blot P, Metezeau P. Tachdjian G, et al. Among authors: cacheux v. Fetal Diagn Ther. 1995 Nov-Dec;10(6):387-92. doi: 10.1159/000264263. Fetal Diagn Ther. 1995. PMID: 8579777

4

Comparative genomic hybridization: technical development and cytogenetic aspects for routine use in clinical laboratories.

Lapierre JM, Cacheux V, Da Silva F, Collot N, Hervy N, Wiss J, Tachdjian G. Lapierre JM, et al. Among authors: cacheux v. Ann Genet. 1998;41(1):56-62. Ann Genet. 1998. PMID: 9599653

5

Comparison of comparative genomic hybridization with conventional karyotype and classical fluorescence in situ hybridization for prenatal and postnatal diagnosis of unbalanced chromosome abnormalities.

Lapierre JM, Cacheux V, Collot N, Da Silva F, Hervy N, Rivet D, Romana S, Wiss J, Benzaken B, Aurias A, Tachdjian G. Lapierre JM, et al. Among authors: cacheux v. Ann Genet. 1998;41(3):133-40. Ann Genet. 1998. PMID: 9833066

6

Detection of 47,XYY trophoblast fetal cells in maternal blood by fluorescence in situ hybridization after using immunomagnetic lymphocyte depletion and flow cytometry sorting.

Cacheux V, Milesi-Fluet C, Tachdjian G, Druart L, Bruch JF, Hsi BL, Uzan S, Nessmann C. Cacheux V, et al. Fetal Diagn Ther. 1992;7(3-4):190-4. doi: 10.1159/000263699. Fetal Diagn Ther. 1992. PMID: 1492908

7

De novo inverted duplication 9p21pter involving telomeric repeated sequences.

Sanlaville D, Baumann C, Lapierre JM, Romana S, Collot N, Cacheux V, Turleau C, Tachdjian G. Sanlaville D, et al. Among authors: cacheux v. Am J Med Genet. 1999 Mar 12;83(2):125-31. doi: 10.1002/(sici)1096-8628(19990312)83:2<125::aid-ajmg8>3.0.co;2-0. Am J Med Genet. 1999. PMID: 10190483 Review.

8

Localization of the CDKN4/p27Kip1 gene to human chromosome 12p12.3.

Martin E, Cacheux V, Cavé H, Lapierre JM, Le Paslier D, Grandchamp B. Martin E, et al. Among authors: cacheux v. Hum Genet. 1995 Dec;96(6):668-70. doi: 10.1007/BF00210296. Hum Genet. 1995. PMID: 8522324

9

Localization of the human coproporphyrinogen oxidase gene to chromosome band 3q12.

Cacheux V, Martasek P, Fougerousse F, Delfau MH, Druart L, Tachdjian G, Grandchamp B. Cacheux V, et al. Hum Genet. 1994 Nov;94(5):557-9. doi: 10.1007/BF00211026. Hum Genet. 1994. PMID: 7959694

10

Altered patterns of DNA methylation on chromosomes from leukemia cell lines: identification of 5-methylcytosines by indirect immunodetection.

Bensaada M, Kiefer H, Tachdjian G, Lapierre JM, Cacheux V, Niveleau A, Métézeau P. Bensaada M, et al. Among authors: cacheux v. Cancer Genet Cytogenet. 1998 Jun;103(2):101-9. doi: 10.1016/s0165-4608(97)00409-3. Cancer Genet Cytogenet. 1998. PMID: 9614907

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