Localization of human ERBA2 to the 3p22→3p24.1 region of chromosome 3 and variable deletion in small cell lung cancerDRABKIN, H; KAO, F.-T; HARTZ, J et al.Proceedings of the National Academy of Sciences of the United States of America. 1988, Vol 85, Num 23, pp 9258-9262, issn 0027-8424Article

The fragile site on chromosome 3SMEETS, D. F. C. M; SCHERES, J. M. J. C; HUSTINX, T. W. J et al.Human genetics. 1984, Vol 67, Num 3, issn 0340-6717, 351Article

The inducible fragile site on chromosome 3BERNAR, J; FUNDERBURK, S. J; SPARKES, R. S et al.Human genetics. 1984, Vol 66, Num 4, issn 0340-6717, 373Article

A new heritable fragile site on human chromosome 3MARKKANEN, A; KNUUTILA, S; DE LA CHAPELLE, A et al.Hereditas (Landskrona). 1983, Vol 99, Num 2, issn 0018-0661, 317Article

The structural gene for transferrin maps to 3q21→3qterHUERRE, C; UZAN, G; GRZESCHIK, K. H et al.Annales de génétique (Paris). 1984, Vol 27, Num 1, pp 5-10, issn 0003-3995Article

Chromosome 3q (22-ter) encodes the human transferrin receptorMILLER, Y. E; JONES, C; SCOGGIN, C et al.American journal of human genetics. 1983, Vol 35, Num 4, pp 573-583, issn 0002-9297Article

Localization of a gene controlling the expression of the human transferrin receptor to the region q12→qter of chromosome 3VAN DE RIJN, M; GEURTS VAN KESSEL, A. H. M; KROEZEN, V et al.Cytogenetics and cell genetics. 1983, Vol 36, Num 3, pp 525-531, issn 0301-0171Article

Familial paracentric inversion inv(3)(q21q25.1): case report and review of the literatureDJALALI, M; STEINBACH, P; BARBI, G et al.Annales de génétique (Paris). 1984, Vol 27, Num 1, pp 41-44, issn 0003-3995Article

Sperm chromosome analysis of a man heterozygous for a pericentric inversion of chromosome 3BALKAN, W; BURNS, K; MARTIN, R. H et al.Cytogenetics and cell genetics. 1983, Vol 35, Num 4, pp 295-297, issn 0301-0171Article

Assignment of the human β-catenin gene (CTNNB1) to 3p22→p21.3 by fluorescence in situ hybridizationVAN HENGEL, J; NOLLET, F; BERX, G et al.Cytogenetics and cell genetics. 1995, Vol 70, Num 1-2, pp 68-70, issn 0301-0171Conference Paper

Localization of the human β-catenin gene (CTNNB1) to 3p21 : a region implicated in tumor developmentKRAUS, C; LIEHR, T; HÜLSKEN, J et al.Genomics (San Diego, Calif.). 1994, Vol 23, Num 1, pp 272-274, issn 0888-7543Article

The role of chromosome 3 deletions in lung cancerKADOWAKI, M. H; FERGUSON, M. K.Lung cancer. 1990, Vol 6, Num 5-6, pp 165-170, issn 0169-5002, 6 p.Article

CONFIRMATION OF THE ASSIGNMENT OF A GLUTATHIONE PEROXIDASE LOCUS TO CHROMOSOME 3 IN MANDONALD LJ; WANG HS; HAMERTON JL et al.1979; CYTOGENET. CELL GENET.; CHE; DA. 1979; VOL. 23; NO 1-2; PP. 141-143; BIBL. 6 REF.Article

DE NOVO del(3)(q2800)ALVAREZ ARRATIA, M. C; RIVERA, H; MOLLER, M et al.Annales de génétique (Paris). 1984, Vol 27, Num 2, pp 109-111, issn 0003-3995Article

A SECOND PATIENT WITH PARTIAL DELETION OF THE SHORT ARM OF CHROMOSOME 3: KARYOTYPE 46,XY,DEL(3) (P25)HIGGINBOTTOM MC; MASCARELLO JT; HASSIN H et al.1982; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1982; VOL. 19; NO 1; PP. 71-73; BIBL. 2 REF.Article

DUPLICATION 3 P SYNDROME: REPORT OF A NEW CASE AND REVIEW OF THE LITERATURECHARROW J; COHEN MM; MEEKER D et al.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 8; NO 4; PP. 431-436; BIBL. 16 REF.Article

DUPLICATION 3Q: SEVERE MANIFESTATIONS IN AN INFANT WITH DUPLICATION OF A SHORT SEGMENT OF 3QROSENFELD W; VERMA RS; JHAVERI RC et al.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 10; NO 2; PP. 187-192; BIBL. 27 REF.Article

A new type of familial chromosome translocation involving 3p and 6q in two unrelated familiesGOTTSCHALL, A; LOSAN, F; PELZ, L et al.Human genetics. 1983, Vol 64, Num 3, issn 0340-6717, 304Article

THE DUP (3) (P25->PTER) SYNDROME: A CASE WITH HOLOPROSENCEPHALYMARTIN NJ; STEINBERG BG.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 14; NO 4; PP. 767-772; BIBL. 16 REF.Article

THE DUP (3Q) SYNDROME: REPORT OF EIGHT CASES AND REVIEW OF THE LITERATURESTEINBACH P; ADKINS WN JR; CASPAR H et al.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 10; NO 2; PP. 159-177; BIBL. 27 REF.Article

CHROMOSOME 3 ABNORMALITIES IN ACUTE NONLYMPHOCYTIC LEUKEMIA (ANLL) WITH ABNORMAL THROMBOPOIESIS: REPORT OF THREE PATIENTS WITH A "NEW" INVERSION ANOMALY AND A FURTHER CASE OF HOMOLOGOUS TRANSLOCATIONBERNSTEIN R; PINTO MR; BEHR A et al.1982; BLOOD; ISSN 0006-4971; USA; DA. 1982; VOL. 60; NO 3; PP. 613-617; BIBL. 24 REF.Article

Human protein synthesis initiation factor elF-4γ is encoded by a single gene (EIF4G) that maps to chromosome 3q27-qterRIQIANG YAN; RHOADS, R. E.Genomics (San Diego, Calif.). 1995, Vol 26, Num 2, pp 394-398, issn 0888-7543Article

Localization of human ARF2 and NCK genes and 13 other NotI-linking clones to chromosome 3 by fluorescence in situ hybridizationVOROBIEVA, N; PROTOPOPOV, A; PROTOPOPOVA, M et al.Cytogenetics and cell genetics. 1995, Vol 68, Num 1-2, pp 91-94, issn 0301-0171Article

Three members of the human cystatin gene superfamily, AHSG, HRG, and KNG, map within one megabase of genomic DNA at 3q27RIZZU, P; BALDINI, A.Cytogenetics and cell genetics. 1995, Vol 70, Num 1-2, pp 26-28, issn 0301-0171Conference Paper

Evidence for the absence of intron H of the histidine-rich glycoprotein (HRG) gene : genetic mapping and in situ localization of HRG to chromosome 3q28-q29HENNIS, B. C; FRANTS, R. R; BAKKER, E et al.Genomics (San Diego, Calif.). 1994, Vol 19, Num 1, pp 195-197, issn 0888-7543Article