DNA methylation profiling of human chromosomes 6, 20 and 22ECKHARDT, Florian; LEWIN, Joern; HAEFLIGER, Carolina et al.Nature genetics. 2006, Vol 38, Num 12, pp 1378-1385, issn 1061-4036, 8 p.Article

Pstl-polymorphism in the human bactericidal permeability increasing protein (BPI) geneHUBACEK, J. A; ASLANIDIS, C; BÜCHLER, C et al.Clinical genetics. 1997, Vol 52, Num 4, issn 0009-9163, p. 249Article

Assignment¹ of cadherin-4(R-cadherin, CDH4) to human chromosome band 20q13.3KOOLS, P; VANHALST, K; VAN ROY, F et al.Cytogenetics and cell genetics. 1999, Vol 86, Num 1, pp 26-27, issn 0301-0171Conference Paper

Assignment¹ of human proliferation associated p100 gene (C20orf1) to human chromosome band 20q11.2 by in situ hybridizationZHANG, Y; HEIDEBRECHT, H.-J; ROTT, A et al.Cytogenetics and cell genetics. 1999, Vol 84, Num 3-4, pp 182-183, issn 0301-0171Article

THE R(20) SYNDROME.HERVA R; SAARINEN I; LEIKKONEN L et al.1977; J. MED. GENET.; G.B.; DA. 1977; VOL. 14; NO 4; PP. 281-283; BIBL. 5 REF.Article

Human hepatocyte nuclear factor-4 (hHNF-4) gene maps to 20q12-q13.1 between PLCG1 and D20S17ARGYROKASTRITIS, A; KAMAKARI, S; KAPSETAKI, M et al.Human genetics. 1997, Vol 99, Num 2, pp 233-236, issn 0340-6717Article

The gene encoding human glutathione synthetase (GSS) maps the long arm of chromosome 20 at band 11.2WEBB, G. C; VASKA, V. L; GALI, R. R et al.Genomics (San Diego, Calif.). 1995, Vol 30, Num 3, pp 617-619, issn 0888-7543Article

Evidence for a prostate cancer linkage to chromosome 20 in 159 hereditary prostate cancer familiesZHENG, Siqun L; JIANFENG XU; ISAACS, Sarah D et al.Human genetics. 2001, Vol 108, Num 5, pp 430-435, issn 0340-6717Article

Assignment of ANGPT4, ANGPT1, and ANGPT2 encoding angiopoietins 4, 1 and 2 to human chromosome bands 20p13, 8q22.3→q23 and 8p23.1, respectively, by in situ hybridization and radiation hybrid mappingGROSIOS, K; LEEK, J. P; MARKHAM, A. F et al.Cytogenetics and cell genetics. 1999, Vol 84, Num 1-2, pp 118-120, issn 0301-0171Article

Hematologic disorders associated with deletions of chromosome 20q : A clinicopathologic study of 107 patientsKURTIN, P. J; DEWALD, G. W; SHIELDS, D. J et al.American journal of clinical pathology. 1996, Vol 106, Num 5, pp 680-688, issn 0002-9173Article

Assignment of the human PTK6 gene encoding a non-receptor protein tyrosine kinase to 20q13.3 by fluorescence in situ hybridizationPARK, S.-H; LEE, K.-H; KIM, H et al.Cytogenetics and cell genetics. 1997, Vol 77, Num 3-4, pp 271-272, issn 0301-0171Article

Molecular cloning of the α3 chain of human type IX collagen : linkage of the gene COL9A3 to chromosome 20q13.3BREWTON, R. G; WOOD, B. M; MAYNE, R et al.Genomics (San Diego, Calif.). 1995, Vol 30, Num 2, pp 329-336, issn 0888-7543Article

Trisomies 8 and 20 in desmoid tumorQI, H; DAL CIN, P; HERNANDEZ, J. M et al.Cancer genetics and cytogenetics. 1996, Vol 92, Num 2, pp 147-149, issn 0165-4608Article

Molecular analysis of ring chromosome 20 syndrome reveals two distinct groups of patientsCONLIN, Laura K; KRAMER, Whitney; SPINNER, Nancy B et al.Journal of medical genetics. 2011, Vol 48, Num 1, pp 1-9, issn 0022-2593, 9 p.Article

Prognosis and gene expression profiling of 20q13-amplified breast cancersGINESTIER, Christophe; CERVERA, Nathalie; CHAFFANET, Max et al.Clinical cancer research. 2006, Vol 12, Num 15, pp 4533-4544, issn 1078-0432, 12 p.Article

Assignment of OVCOV1 (alias CGI-15) to human chromosome 20 band q13.1 →q13.2 by fluorescent in situ hybridizationLEACH, R; DUNIEC-DMUCHOWSKI, Z; TANAKA, T et al.Cytogenetics and cell genetics. 2001, Vol 94, Num 3-4, pp 252-253, issn 0301-0171Article

Chromosomes 19 and 20 reportGEJMAN, P. V.American journal of medical genetics. 1999, Vol 88, Num 3, issn 0148-7299, p. 271Conference Paper

Physical and linkage mapping of the gene for the a3 chain of type IX collagen, COL9A3, to human chromosome 20q13.3TILLER, G. E; WARMAN, M. L; GONG, Y et al.Cytogenetics and cell genetics. 1998, Vol 81, Num 3-4, pp 205-207, issn 0301-0171Conference Paper

Assignment of human elongation factor 1α genes : EEF1A maps to chromosome 6q14 and EEF1A2 to 20q13.3LUND, A; KNUDSEN, S. M; VISSING, H et al.Genomics (San Diego, Calif.). 1996, Vol 36, Num 2, pp 359-361, issn 0888-7543Article

Isolation of the human beaded-filament structural protein 1 gene (BFSP1) and assignment to chromosome 20p11.23-p12.1RENDTORFF, N. D; HANSEN, C; SILAHTAROGLU, A et al.Genomics (San Diego, Calif.). 1998, Vol 53, Num 1, pp 114-116, issn 0888-7543Article

The telomere-associated DNA from human chromosome 20p contains a pseudotelomere structure and shares sequences with the subtelomeric regions of 4q and 18pCHUTE, I; LE, Y; ASHLEY, T et al.Genomics (San Diego, Calif.). 1997, Vol 46, Num 1, pp 51-60, issn 0888-7543Article

Deletion of chromosome 20q associated with hypereosinophilic syndrome : A report of two casesBRIGAUDEAU, C; LIOZON, E; BERNARD, P et al.Cancer genetics and cytogenetics. 1996, Vol 87, Num 1, pp 82-84, issn 0165-4608Article

REGIONAL ASSIGNMENT OF THE ADA LOCUS ON 20 Q 13.2->QTER BY GENE DOSAGE STUDIESPHILIP T; LENOIR G; ROLLAND MO et al.1980; CYTOGENET. CELL GENET.; CHE; DA. 1980; VOL. 27; NO 2-3; PP. 187-189; BIBL. 9 REF.Article

CHROMOSOME 20 EN ANNEAU: UN NOUVEAU SYNDROME.JALBERT P; JALBERT H; SELE B et al.1977; ANN. GENET.; FR.; DA. 1977; VOL. 20; NO 4; PP. 258-262; ABS. ANGL.; BIBL. 24 REF.Article

REGIONAL MAPPING OF ADA AND ITP ON HUMAN CHROMOSOME 20: CYTOGENETIC AND SOMATIC CELL STUDIES IN AN X/20 TRANSLOCATIONMOHANDAS T; SPARKES RS; PASSAGE MB et al.1980; CYTOGENET. CELL GENET.; CHE; DA. 1980; VOL. 26; NO 1; PP. 28-35; BIBL. 2 P.Article