Familial dup(5)(q15q21) associated with normal and abnormal phenotypesLI, S.-Y; GIBSON, L. H; GOMEZ, K et al.American journal of medical genetics. 1998, Vol 75, Num 1, pp 75-77, issn 0148-7299Article

Cytogenetic and molecular diagnosis of chromosome 5 deletions in myelodysplasiaWESTBROOK, C. A; HSU, W.-T; CHYNA, B et al.British journal of haematology. 2000, Vol 110, Num 4, pp 847-855, issn 0007-1048Article

Familial double pericentric inversion of chromosome 5 with some features of cri-du-chat syndromeGOODART, S. A; BUTLER, M. G; OVERHAUSER, J et al.Human genetics. 1996, Vol 97, Num 6, pp 802-807, issn 0340-6717Article

Partial deletion of the long arm of chromosome 5 : A fluorescence in situ hydridization study using band-specific painting probes generated by chromosome microdissectionTIGAUD, I; CHARRIN, C; BERGER, R et al.Cancer genetics and cytogenetics. 1996, Vol 89, Num 2, pp 126-128, issn 0165-4608Article

Blood consult: treating del(5q) myelodysplastic syndromesMUKHERJEE, Sudipto; TIU, Ramon V; SEKERES, Mikkael A et al.Blood. 2012, Vol 119, Num 2, pp 342-344, issn 0006-4971, 3 p.Article

Circulating t(2;5)-positive cells can be detected in cord blood of healthy newbornsLAURENT, C; LOPEZ, C; DESJOBERT, C et al.Leukemia. 2012, Vol 26, Num 1, pp 188-190, issn 0887-6924, 3 p.Article

Terminal deletion of chromosome 5p in a patient with phenotypical features of Lujan-Fryns syndromeSTATHOPULU, E; OGILVIE, C. Mackie; FLINTER, F. A et al.American journal of medical genetics. 2003, Vol 119A, Num 3, pp 363-366, issn 0148-7299, 4 p.Article

Identification of a group of AML/MDS patients with a relatively favorable prognosis who have chromosome 5 and/or 7 abnormalitiesESTEY, E. H; PIERCE, S; KEATING, M. J et al.Haematologica (Roma). 2000, Vol 85, Num 3, pp 246-249, issn 0390-6078Article

A case of de novo interstitial deletion of chromosome 5(q33q34)GILTAY, J. C; GERSSEN-SCHOORL, K. B. J; LUITSE, G. H. J et al.Clinical genetics. 1997, Vol 52, Num 3, pp 173-176, issn 0009-9163Article

The human POP2 gene : Identification, sequencing, and mapping to the critical region of the 5q- syndromeFIDLER, C; WAINSCOAT, J. S; BOULTWOOD, J et al.Genomics (San Diego, Calif.). 1999, Vol 56, Num 1, pp 134-136, issn 0888-7543Article

Proximal partial 5p trisomy resulting from a maternal (19;5) insertionLORDA-SANCHEZ, I; URIOSTE, M; VILLA, A et al.American journal of medical genetics. 1997, Vol 68, Num 4, pp 476-480, issn 0148-7299Article

t(1;5)(q23;q33) in a patient with high-risk B-lineage acute lymphoblastic leukemiaBARRIGA, F; BERTIN, P; LEGÜES, E et al.Cancer genetics and cytogenetics. 1996, Vol 87, Num 1, pp 4-6, issn 0165-4608Article

t(5;12)(q31;q24) in childhood acute lymphoblastic leukemiaTUSELL, L; CABALLIN, M. R; COLL, M. D et al.Cancer genetics and cytogenetics. 1996, Vol 89, Num 2, pp 163-165, issn 0165-4608Article

De novo balanced 5;21 translocation in a child with acrobrachycephaly, ventriculomegaly, pulmonary stenosis, ectopic anus and mental retardationHORDNES, K; ENGEBRETSEN, L. F; KNUDTZON, J et al.Clinical genetics. 1995, Vol 48, Num 6, pp 321-323, issn 0009-9163Article

Lenalidomide for del(5q) and Non-del(5q) Myelodysplastic SyndromesGIAGOUNIDIS, Aristoteles A. N.Seminars in hematology. 2012, Vol 49, Num 4, pp 312-322, issn 0037-1963, 11 p.Article

Syndromes myélodysplasiques avec délétion du bras long du chromosome 5 = Myelodysplasic syndromes associated with 5q-deletionsFRISAN, Emilie; VIGUIE, Franck; DREYFUS, Francois et al.Hématologie (Montrouge). 2008, Vol 14, Num 2, pp 112-115, issn 1264-7527, 4 p.Article

Interstitial deletion of long arm of chromosome no. 5 with growth hormone deficiency: an emerging syndrome?KRISHNA, J; MYERS, T. L; BOURGEOIS, M. J et al.Clinical genetics. 1997, Vol 51, Num 1, pp 48-51, issn 0009-9163Article

A new translocation, t(5;21)(q13;q22) in acute myelogenous leukemiaGOGINENI, S. K; DA COSTA, M; VERMA, R. S et al.Cancer genetics and cytogenetics. 1996, Vol 88, Num 2, pp 167-169, issn 0165-4608Article

Translocations and deletions of 5q13.1 in myelodysplasia and acute myelogenous leukemia : Evidence for a novel critical locusFAIRMAN, J; RUI YU WANG; LIANG, H et al.Blood. 1996, Vol 88, Num 6, pp 2259-2266, issn 0006-4971Article

Unbalanced segregation of a complex four-break 5q23-31 insertion in the 5p13 band in a malformed childGIARDINO, Daniela; FINELLI, Palma; AMICO, Francesco Paolo et al.European journal of human genetics. 2004, Vol 12, Num 6, pp 455-459, issn 1018-4813, 5 p.Article

Clinical and molecular characterisation of 80 patients with 5p deletion: genotype-phenotype correlationMAINARDI, P. Cerruti; PERFUMO, C; CALI, A et al.Journal of medical genetics. 2001, Vol 38, Num 3, pp 151-158, issn 0022-2593Article

Duplication within chromosome 5q characterized by fluorescence in situ hybridizationMOWAT, D; JAUCH, A; ROBSON, L et al.American journal of medical genetics. 1999, Vol 83, Num 5, pp 361-364, issn 0148-7299Article

Tetrasomy 5p mosaicism due to an extra i(5p) in a severely affected girlLORDA-SANCHEZ, I; VILLA, A; URIOSTE, M et al.American journal of medical genetics. 1997, Vol 68, Num 4, pp 481-484, issn 0148-7299Article

5q-, Twenty-five years later : A synopsisVAN DEN BERGHE, H; MICHAUX, L.Cancer genetics and cytogenetics. 1997, Vol 94, Num 1, pp 1-7, issn 0165-4608Article

Unbalanced translocation in a mother and her son in one of two 5;10 translocation familiesBARBER, J. C. K; TAMPLE, I. K; CAMPBELL, P. L et al.American journal of medical genetics. 1996, Vol 62, Num 1, pp 84-90, issn 0148-7299Article