BRIEF COMMUNICATION: SPECIFICITY OF THE 5 Q-CHROMOSOME IN A DISTINCT TYPE OF REFRACTORY ANEMIA.VERHEST A; VAN SCHOUBROECK F; WITTEK M et al.1976; J. NATION. CANCER INST.; U.S.A.; DA. 1976; VOL. 56; NO 5; PP. 1053-1054; BIBL. 8 REF.Article

Assignment of the gene for human arylsulfatase B, ARSB, to chromosome region 5p11→5qterFIDZIANSKA, E; ABRAMOWICZ, T; CZARTORYSKA, B et al.Cytogenetics and cell genetics. 1984, Vol 38, Num 2, pp 150-151, issn 0301-0171Article

Cytogenetic evidence of clonal evolution in a case of hemopoietic dysplasia with a 5q- chromosome = Mise en évidence cytogénétique de l'évolution clonale dans un cas de dysplasie hémopoïétique avec chromosome 5q9cTANIWAKI, M; EDAGAWA, J; SONODA, Y et al.Cancer genetics and cytogenetics. 1983, Vol 10, Num 1, pp 59-65, issn 0165-4608Article

International workshop on human chromosome 5 mapping 1992Cytogenetics and cell genetics. 1992, Vol 61, Num 4, pp 225-242, issn 0301-0171Conference Proceedings

An anonymous DNA segment pTP5E (D5S70) maps to the long arm of chromosome 5 and identifies a Taq I polymorphismFARBER, R. A; PHALEN, T; NEUMAN, W. L et al.Nucleic acids research. 1988, Vol 16, Num 5, issn 0305-1048, 2360, part BArticle

A PROPOS D'UNE OBSERVATION DE MALADIE DU CRI DU CHAT.CASTEL Y; TOUDIC L; RIVIERE D et al.1977; REV. INTERNATION. PEDIATR.; FR.; DA. 1977; NO 76; PP. 29-42; BIBL. 19 REF.Article

CYTOGENETIC RECOMBINANTS FROM A FEMALE CARRYING A PARACENTRIC INVERSION OF THE SHORT ARM OF CHROMOSOME NUMBER 5VALCARCEL E; BENITEZ J; MARTINEZ P et al.1983; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1983; VOL. 63; NO 1; PP. 78-81; BIBL. 12 REF.Article

DELETION OF THE SHORT ARM OF CHROMOSOME 5 FROM A SUBJECT WITH CRI-DU-CHAT SYNDROME. REPOSITORY IDENTIFICATION NO. GM71.BREG WR; ARONSON MM; GREENE AE et al.1976; CYTOGENET. CELL GENET.; SWITZ.; DA. 1976; VOL. 17; NO 4; PP. 239-240; BIBL. 3 REF.Article

DEL (5P) WITHOUT "CRI DU CHAT" PHENOTYPEBACCICHETTI C.1982; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1982; VOL. 60; NO 4; PP. 389Article

CYTOGENETIQUE DU SYNDROME DU CRI DU CHATZHOU HUANGENG; KANG XUEZHEN; ZHANG QIANQIAN et al.1982; ACTA GENET. SIN.; CHN; DA. 1982; VOL. 9; NO 1; PP. 20-23; ABS. ENG; BIBL. 7 REF.Article

Interstitial delection of band q12 of chromosome 5DUDIN, G; ALEXANDER, D; TALJ, F et al.Clinical genetics. 1984, Vol 25, Num 5, pp 455-458, issn 0009-9163Article

5q-syndrome: complete response to chemotherapyCONNEALLY, E; SHERRINGTON, P; FISCHER, P et al.Clinical and laboratory haematology. 1990, Vol 12, Num 1, pp 101-103, issn 0141-9854, 3 p.Article

De novo t(4;5) (q3100; q2200) with del (5) (q1500; q2200). Tentative delineation of a 5q monosomy syndrome and assignment of the critical segmentRIVERA, H; ROLON, A; SANCHEZ-CORONA, J et al.Clinical genetics. 1985, Vol 27, Num 1, pp 105-109, issn 0009-9163Article

ABOLISHED PRODUCTION OF INTERFERON BY LEUCOCYTES OF PATIENTS WITH THE ACQUIRED CYTOGENETIC ABNORMALITIES 5Q- OR -5 IN SECONDARY AND DE-NOVO ACUTE NON-LYMPHOCYTIC LEUKAEMIAPEDERSEN BJERGAARD J; HAAHR S; PHILIP P et al.1980; BR. J. HAEMATOL.; ISSN 0007-1048; GBR; DA. 1980; VOL. 46; NO 2; PP. 211-223; BIBL. 2 P.Article

Hunter's disease in a girl: association with X:5 chromosomal translocation disrupting the Hunter geneMOSSMAN, J; BLUNT, S; STEPHENS, R et al.Archives of disease in childhood. 1983, Vol 58, Num 11, pp 911-915, issn 0003-9888Article

Refined mapping of the G_M2 activator protein (GM2A) locus to 5q31.3-q33.1, distal to the spinal muscular atrophy locusHENG, H. H. Q; BEI XIE; XIAO-MEI SHI et al.Genomics (San Diego, Calif.). 1993, Vol 18, Num 2, pp 429-431, issn 0888-7543Article

A new RFLP for L1.4 (D5S4) an anonymous genomic clone localised to chromosome 5BAILEY, C. J; RIDER, S. H; BODMER, W. F et al.Nucleic acids research. 1987, Vol 15, Num 16, issn 0305-1048, 6762Article

Trisomy 5 mosaicism in amniotic fluid with normal outcomeCASAMASSIMA, A. C; WILMOT, P. L; MAHONEY, M. J et al.Clinical genetics. 1989, Vol 35, Num 4, pp 282-284, issn 0009-9163, 3 p.Article

Interleukin 4 is at 5q31 and interleukin 6 is at 7p15SUTHERLAND, G. R; BAKER, E; VADAS, M. A et al.Human genetics. 1988, Vol 79, Num 4, pp 335-337, issn 0340-6717Article

Consistent loss of the D5S89 locus mapping telomeric to the interleukin gene cluster and centromeric to EGR-1 in patients with 5q^- chromosomeLALITHA NAGARAJAN; JIRI ZAVADIL; WILLMAN, C. L et al.Blood. 1994, Vol 83, Num 1, pp 199-208, issn 0006-4971Article

A new apparently folate sensitive fragile site, 5q35HOWELL, R. T; MCDERMOTT, A; EVANS, J. L et al.Journal of medical genetics. 1990, Vol 27, Num 8, pp 527-528, issn 0022-2593Article

Chromosome mapping of 11 human pobes in the region 5q2→q3 by fluorescence in situ hybridizationRICHARD, F; MULERIS, M; DUTRILLAUX, B et al.Cytogenetics and cell genetics. 1995, Vol 68, Num 3-4, pp 207-210, issn 0301-0171Conference Paper

Assignment of the human α-catenin gene (CTNNA1) to chromosome 5q21-q22MCPHERSON, J. D; MORTON, R. A; EWING, C. M et al.Genomics (San Diego, Calif.). 1994, Vol 19, Num 1, pp 188-190, issn 0888-7543Article

Human cyclin B1 gene (CCNB1) assigned to chromosome 5 (q13-qter)MILATOVICH, A; FRANCKE, U.Somatic cell and molecular genetics. 1992, Vol 18, Num 3, pp 303-307, issn 0740-7750Article

The gene coding for glial cell line derived neurotrophic factor (GDNF) maps to chromosome 5p12-p13.1SCHINDELHAUER, D; SCHUFFENHAUER, S; GASSER, T et al.Genomics (San Diego, Calif.). 1995, Vol 28, Num 3, pp 605-607, issn 0888-7543Article