L'hybridation in situ fluorescente en cancérologie = Fluorescent in situ hybridization (FISH) in oncologyROMANA, S. P.Bulletin du cancer. 1998, Vol 85, Num 3, pp 209-215, issn 0007-4551Article

Indications de l'analyse des chromosomes et de l'ADN pour le diagnostic des maladies génétiques = Indications for chromosome and DNA analysis for diagnosis of genetic diseasesROMANA, S.-P; GERARD, B.La Revue du praticien (Paris). 1997, Vol 47, Num 11, pp 1241-1252, issn 0035-2640Article

Complex chromosomal rearrangement and intracytoplasmic sperm injection : A Case ReportJOLY-HELAS, G; DE LA ROCHEBROCHARD, C; MOUSSET-SIMEON, N et al.Human reproduction (Oxford. Print). 2007, Vol 22, Num 5, pp 1292-1297, issn 0268-1161, 6 p.Article

High frequency of t(12;21) in childhood B-lineage acute lymphoblastic leukemiaROMANA, S. P; POIREL, H; LECONIAT, M et al.Blood. 1995, Vol 86, Num 11, pp 4263-4269, issn 0006-4971Article

NUP98-HMGB3: a novel oncogenic fusionPETIT, A; RAGU, C; PENARD-LACRONIQUE, V et al.Leukemia. 2010, Vol 24, Num 3, pp 654-658, issn 0887-6924, 5 p.Article

A CGH study of 27 patients with CHARGE associationSANLAVILLE, D; ROMANA, S. P; TURLEAU, C et al.Clinical genetics. 2002, Vol 61, Num 2, pp 135-138, issn 0009-9163Article

Molecular analysis of chromosomal breakpoints in three examples of chromosomal translocation involving the TEL geneROMANA, S. P; POIREL, H; DELLA VALLE, V et al.Leukemia. 1999, Vol 13, Num 11, pp 1754-1759, issn 0887-6924Conference Paper

Fusion of ZMIZ1 to ABL1 in a B-cell acute lymphoblastic leukaemia with a t(9;10)(q34;q22.3) translocationSOLERL, G; RADFORD-WEISS, I; BEN-ABDELALI, R et al.Leukemia. 2008, Vol 22, Num 6, pp 1278-1280, issn 0887-6924, 3 p.Article

The TEL gene products: nuclear phosphoproteins with DNA binding propertiesPOIREL, H; OURY, C; GHYSDAEL, J et al.Oncogene (Basingstoke). 1997, Vol 14, Num 3, pp 349-357, issn 0950-9232Article

The t(12;21) of acute lymphoblastic leukemia results in a tel-AML1 gene fusionROMANA, S. P; MAUCHAUFFE, M; LE CONIAT, M et al.Blood. 1995, Vol 85, Num 12, pp 3662-3670, issn 0006-4971Article

NUP214-ABL1 amplification in t(5;14)/HOX11L2-positive ALL present with several forms and may have a prognostic significanceBALLERINI, P; BUSSON, M; FASOLA, S et al.Leukemia. 2005, Vol 19, Num 3, pp 468-470, issn 0887-6924, 3 p.Article

PMX2B, a new candidate gene for hirschsprung's diseaseBENAILLY, H. K; LAPIERRE, J. M; LAUDIER, B et al.Clinical genetics. 2003, Vol 64, Num 3, pp 204-209, issn 0009-9163, 6 p.Article

Comparative genomic hybridisation in mentally retarded patients with dysmorphic features and a normal karyotypeJOLY, G; LAPIERRE, J-M; ROMANA, S. P et al.Clinical genetics. 2001, Vol 60, Num 3, pp 212-219, issn 0009-9163Article

Partial duplication of HRX in acute leukemia with trisomy 11BERNARD, O. A; ROMANA, S. P; SCHICHMAN, S. A et al.Leukemia. 1995, Vol 9, Num 9, pp 1487-1490, issn 0887-6924Article

NUP98 rearrangements in hematopoietic malignancies : a study of the Groupe francophone de cytogénétique hématologiqueROMANA, S. P; RADFORD-WEISS, I; MOZZICONACCI, M.-J et al.Leukemia. 2006, Vol 20, Num 4, pp 696-706, issn 0887-6924, 11 p.Article

La CGH microarray : principe et applications en pathologie constitutionnelle = Microarray CGH : principle and use for constitutional disordersSANLAVILLE, D; LAPIERRE, J. M; COQUIN, A et al.Archives de pédiatrie (Paris). 2005, Vol 12, Num 10, pp 1515-1520, issn 0929-693X, 6 p.Article

Pure partial 7p trisomy including the TWIST, HOXA, and GLI3 genesMEGARBANE, A; LE LORC'H, M; ROMANA, S. P et al.Journal of medical genetics. 2001, Vol 38, Num 3, pp 178-182, issn 0022-2593Article

Secondary acute myeloblastic leukemia with t(16;21)(q24;q22) involving the AML1 geneBERGER, R; LE CONIAT, M; ROMANA, S. P et al.Hematology and cell therapy (Print). 1996, Vol 38, Num 2, pp 183-186, issn 1269-3286Conference Paper

A novel translocation, t(9;11)(q33;q23) involving the HRX gene in an acute monocytic leukemia = Une nouvelle translocation, t(9;11)(q33;q23) impliquant le gène HRX dans une leucémie aiguë monocytaireLE CONIAT, M; ROMANA, S. P; BERNARD, O et al.Comptes rendus de l'Académie des sciences. Série 3, Sciences de la vie. 1993, Vol 316, Num 7, pp 692-697, issn 0764-4469Article

Chromosome 11p15 Paternal Isodisomy in Focal Forms of Neonatal HyperinsulinismDAMAJ, L; LE LORCH, M; DE LONLAY, P et al.The Journal of clinical endocrinology and metabolism. 2008, Vol 93, Num 12, pp 4941-4947, issn 0021-972X, 7 p.Article

Molecular cytogenetic analysis of five 2q37 deletions : refining the brachydactyly candidate regionCHAABOUNI, M; LE MERRER, M; RAOUL, O et al.European journal of medical genetics. 2006, Vol 49, Num 3, pp 255-263, issn 1769-7212, 9 p.Article

Le caryotype spectral (SKY) : principe, avantages et limites en cytogénétique constitutionnelle et tumorale = Spectral karyotyping (SKY): principle, avantages and limitationsBELAUD-ROTUREAU, M. A; ELGHEZAL, H; BERNARDIN, C et al.Annales de biologie clinique (Paris). 2003, Vol 61, Num 2, pp 139-146, issn 0003-3898, 8 p.Article

Molecular characterization of partial trisomy 16q24.1-qter: Clinical report and review of the literatureBRISSET, S; JOLY, G; ROMANA, S. P et al.American journal of medical genetics. 2002, Vol 113, Num 4, pp 339-345, issn 0148-7299, 7 p.Article

Deletion of the short arm of chromosome 12 is a secondary event in acute lymphoblastic leukemia with t(12;21)ROMANA, S. P; LE CONIAT, M; POIREL, H et al.Leukemia. 1996, Vol 10, Num 1, pp 167-170, issn 0887-6924Article

Translocation t(3;22)(q27;q11) in non-Hodgkin's malignant lymphoma : chromosome painting and molecular studiesHEBERT, J; ROMANA, S. P; HILLION, J et al.Leukemia. 1993, Vol 7, Num 12, pp 1971-1974, issn 0887-6924Article