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Ring chromosome 5FLANNERY, D. B; ROGERS, W. G; BYRD, J. R et al.Clinical genetics. 1988, Vol 34, Num 1, pp 74-78, issn 0009-9163Article

De novo inv(5)(p15q22), del(5)(p15) in a boy with cri du chat syndromeRIVERA, H; VELAZQUEZ, R; GARCIA-ESQUIVEL, L et al.Journal of medical genetics. 1987, Vol 24, Num 3, issn 0022-2593, 186Article

High resolution analysis of the 5q- marker chromosome in refractory anemiaMITELMAN, F; MANOLOVA, Y; MANOLOV, G et al.Hereditas (Landskrona). 1986, Vol 105, Num 1, pp 49-54, issn 0018-0661Article

inv(5)(p13q13) in a four generation pedigreeVARGAS-MOYEDA, E; RIVERA, H; GARCIA-CRUZ, D et al.Journal de génétique humaine. 1987, Vol 35, Num 4, pp 305-308, issn 0021-7743Article

Delection 5q35.3STRATTON, R. F; TEDROWE, N. A; TOLWORTHY, J. A et al.American journal of medical genetics. 1994, Vol 51, Num 2, pp 150-152, issn 0148-7299Article

Constitutional del(5)(q23.3q31.1)RIVERA, H; GARCIA-ESQUIVEL, L; MOLLER, M et al.Annales de génétique (Paris). 1987, Vol 30, Num 2, pp 91-93, issn 0003-3995Article

Evidence for a distinct region causing a cat-like cry in patients with 5p deletionsGERSH, M; GOODART, S. A; PASZTOR, L. M et al.American journal of human genetics. 1995, Vol 56, Num 6, pp 1404-1410, issn 0002-9297Article

Molecular analysis of a case of meiotic recombination leading to cri-du-chat syndromeDOBBS, M; OVERHAUSER, J; WASMUTH, J. J et al.Cytogenetics and cell genetics. 1988, Vol 47, Num 1-2, pp 5-7, issn 0301-0171Article

Terminal deletion of the short arm of chromosome 5BACCICHETTI, C; LENZINI, E; ARTIFONI, L et al.Clinical genetics. 1988, Vol 34, Num 4, pp 219-223, issn 0009-9163Article

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

5q: syndrome in a childUYTTEBROECK, A; BROCK, P; DE GROOTE, B et al.Cancer genetics and cytogenetics. 1995, Vol 80, Num 2, pp 121-123, issn 0165-4608Article

5q-anomaly in acute lymphoblastic leukemiaBERGER, R; LE CONIAT, M; DERRE, J et al.Cancer genetics and cytogenetics. 1992, Vol 61, Num 2, pp 201-203, issn 0165-4608Article

Molecular definition of deletions of different segments of distal 5p that result in distinct phenotypic featuresCHURCH, D. M; BENGTSSON, U; NIELSEN, K. V et al.American journal of human genetics. 1995, Vol 56, Num 5, pp 1162-1172, issn 0002-9297Article

A case report of a de novo tandem duplication (Sp) (p14→pter)CHIA, N. L; BOUSFIELD, L. R; JOHNSON, B. H et al.Clinical genetics. 1987, Vol 31, Num 2, pp 65-69, 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

5p- chromosome : evidence for complex interstitial breaks in a case of refractory anemia with excess blastsNAGARAJAN, L; LIAN ZHAO; XIAOYAN LU et al.Cancer genetics and cytogenetics. 1994, Vol 74, Num 1, pp 8-12, issn 0165-4608Article

A new case of complete trisomy 5p with isochromosom 5p associated with a de novo translocation t(5;8)(q11;p23)FUJITA, M; LEMAIRE, F; CASANOVA, R et al.Clinical genetics. 1994, Vol 45, Num 6, pp 305-307, issn 0009-9163Article

Linkage mapping detects two secondary microdeletions in cell hydrig HHW1064, used to isolate DNA probes from within 5q11.2→q13.3BERNARD, L. E; MCPHERSON, J. D; WASMUTH, J. J et al.Cytogenetics and cell genetics. 1993, Vol 64, Num 1, pp 46-48, issn 0301-0171Article

Morphométrie encéphalique en IRM dans la maladie du cri du chat : à propos de sept patients, avec revue de la littérature = Brain morphometry using MRI in cat cry syndrome.About seven patients with revue of the literatureTAMRAZ, J; RETHORE, M.-O; LEJEUNE, J et al.Annales de génétique (Paris). 1993, Vol 36, Num 2, pp 75-87, issn 0003-3995Article

Complex chromosomal rearrangements in an unusual variant of hairy cell leukemiaNACHEVA, E; FISCHER, P; O'CONNOR, S et al.Cancer genetics and cytogenetics. 1992, Vol 62, Num 2, pp 186-190, issn 0165-4608Article