Receveur A - Search Results

1

Burkitt-type acute leukemia in a patient with B-prolymphocytic leukemia: evidence for a common origin.

Nguyen-Khac F, Davi F, Receveur A, Maloum K, Morel V, Le Garff-Tavernier M, Ong J, Berger R, Leblond V, Merle-Béral H. Nguyen-Khac F, et al. Among authors: receveur a. Cancer Genet Cytogenet. 2005 May;159(1):74-8. doi: 10.1016/j.cancergencyto.2004.09.016. Cancer Genet Cytogenet. 2005. PMID: 15860362

2

Trisomy 4 associated with double minute chromosomes and MYC amplification in acute myeloblastic leukemia.

Receveur A, Ong J, Merlin L, Azgui Z, Merle-Béral H, Berger R, Nguyen-Khac F. Receveur A, et al. Ann Genet. 2004 Oct-Dec;47(4):423-7. doi: 10.1016/j.anngen.2004.08.004. Ann Genet. 2004. PMID: 15581842 Review.

3

Characterization of quantitative chromosomal abnormalities in renal cell carcinomas by interphase four-color fluorescence in situ hybridization.

Receveur AO, Couturier J, Molinié V, Vieillefond A, Desangles F, Guillaud-Bataille M, Danglot G, Coullin P, Bernheim A. Receveur AO, et al. Cancer Genet Cytogenet. 2005 Apr 15;158(2):110-8. doi: 10.1016/j.cancergencyto.2004.08.019. Cancer Genet Cytogenet. 2005. PMID: 15796957

4

Multiple excitation confocal analysis of targets in nuclei of cytogenetic preparations.

Kahn E, Receveur A, Coullin P, Frouin F, Blanco-Soulas C, Todd-Pokropek A, Bernheim A. Kahn E, et al. Among authors: receveur a. Anal Quant Cytol Histol. 2004 Feb;26(1):1-6. Anal Quant Cytol Histol. 2004. PMID: 15032074

5

Microdeletion at chromosome 4q21 defines a new emerging syndrome with marked growth restriction, mental retardation and absent or severely delayed speech.

Bonnet C, Andrieux J, Béri-Dexheimer M, Leheup B, Boute O, Manouvrier S, Delobel B, Copin H, Receveur A, Mathieu M, Thiriez G, Le Caignec C, David A, de Blois MC, Malan V, Philippe A, Cormier-Daire V, Colleaux L, Flori E, Dollfus H, Pelletier V, Thauvin-Robinet C, Masurel-Paulet A, Faivre L, Tardieu M, Bahi-Buisson N, Callier P, Mugneret F, Edery P, Jonveaux P, Sanlaville D. Bonnet C, et al. Among authors: receveur a. J Med Genet. 2010 Jun;47(6):377-84. doi: 10.1136/jmg.2009.071902. J Med Genet. 2010. PMID: 20522426

6

Involvement of interstitial telomeric sequences in two new cases of mosaicism for autosomal structural rearrangements.

Lévy J, Receveur A, Jedraszak G, Chantot-Bastaraud S, Renaldo F, Gondry J, Andrieux J, Copin H, Siffroi JP, Portnoï MF. Lévy J, et al. Among authors: receveur a. Am J Med Genet A. 2015 Feb;167A(2):428-33. doi: 10.1002/ajmg.a.36857. Epub 2014 Nov 26. Am J Med Genet A. 2015. PMID: 25428228

7

Early prenatal diagnosis of alveolar capillary dysplasia with misalignment of pulmonary veins due to a 16q24.1 deletion.

Puisney-Dakhli C, Gubana F, Petit F, Bouchghoul H, Gautier V, Martinovic J, Tachdjian G, Receveur A. Puisney-Dakhli C, et al. Among authors: receveur a. Am J Med Genet A. 2021 May;185(5):1494-1497. doi: 10.1002/ajmg.a.62105. Epub 2021 Jan 31. Am J Med Genet A. 2021. PMID: 33522073

8

Azoospermia and trisomy 18p syndrome: a fortuitous association? A patient report and a review of the literature.

Jedraszak G, Copin H, Demailly M, Quibel C, Leclerc T, Gallet M, Benkhalifa M, Receveur A. Jedraszak G, et al. Among authors: receveur a. Mol Cytogenet. 2015 Jun 4;8:34. doi: 10.1186/s13039-015-0141-8. eCollection 2015. Mol Cytogenet. 2015. PMID: 26042156 Free PMC article.

9

Detecting single DNA copy number variations in complex genomes using one nanogram of starting DNA and BAC-array CGH.

Guillaud-Bataille M, Valent A, Soularue P, Perot C, Inda MM, Receveur A, Smaïli S, Roest Crollius H, Bénard J, Bernheim A, Gidrol X, Danglot G. Guillaud-Bataille M, et al. Among authors: receveur a. Nucleic Acids Res. 2004 Jul 29;32(13):e112. doi: 10.1093/nar/gnh108. Nucleic Acids Res. 2004. PMID: 15284333 Free PMC article.

10

Syndromic mental retardation with thrombocytopenia due to 21q22.11q22.12 deletion: Report of three patients.

Katzaki E, Morin G, Pollazzon M, Papa FT, Buoni S, Hayek J, Andrieux J, Lecerf L, Popovici C, Receveur A, Mathieu-Dramard M, Renieri A, Mari F, Philip N. Katzaki E, et al. Among authors: receveur a. Am J Med Genet A. 2010 Jul;152A(7):1711-7. doi: 10.1002/ajmg.a.33478. Am J Med Genet A. 2010. PMID: 20578134

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