MALFORMATIVE SYNDROME ASSOCIATED WITH A RING 10 CHROMOSOME AND A TRANSLOCATED 10Q/19 CHROMOSOMEFRYNS JP; DE BOECK K; JAEKEN J et al.1978; HUM. GENET.; DEU; DA. 1978; VOL. 43; NO 2; PP. 239-244; BIBL. 9 REF.Article

VARIATION IN CHROMOSOME 19GARDNER HA; WOOD EM.1979; J. MED. GENET.; GBR; DA. 1979; VOL. 16; NO 1; PP. 79-80; BIBL. 6 REF.Article

BALANCED RECIPROCAL WHOLE-ARM TRANSLOCATION T(1;19) IN THREE GENERATIONS.SCHOBER AM; FONATSCH C.1978; HUM. GENET.; DEU; DA. 1978; VOL. 42; NO 3; PP. 349-352; BIBL. 9 REF.Article

19q Distal trisomy due to a de nuovo (19; 22) (q 13.2; p11) translocationRIVAS, F; GARCIÁ-CRUZ, D; RIVERA, M et al.Annales de génétique (Paris). 1985, Vol 28, Num 2, pp 113-115, issn 0003-3995Article

PACHYTENE CHROMOMERE MAPO OF HUMAN CHROMOSOMES 19 AND 20HUNGERFORD DA; HUNGERFORD AM.1980; CYTOGENET. CELL GENET.; CHE; DA. 1980; VOL. 27; NO 2-3; PP. 197-200; BIBL. 10 REF.Article

INVERSION 19 AND ISOCHROMOSOME SHORT ARM 17 OR 18.NIELSEN J; HOMMA A; HOLM V et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 37; NO 3; PP. 347-350; BIBL. 6 REF.Article

TRISOMY FOR THE DISTAL THIRD OF THE LONG ARM OF CHROMOSOME 19 IN BROTHER AND SISTERSCHMID W.1979; HUM. GENET.; DEU; DA. 1979; VOL. 46; NO 3; PP. 263-270; BIBL. 1 REF.Article

DISTAL 19Q DUPLICATIONZONANA J; BROWN MG; MAGENIS RE et al.1982; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1982; VOL. 60; NO 3; PP. 267-270; BIBL. 8 REF.Article

HUMAN TELOMERIC 6; 19 TRANSLOCATION CHROMOSOME WITH A TENDENCY TO BREACH AT THE FUSION POINTDRETS ME; THERMAN E.1983; CHROMOSOMA; ISSN 0009-5915; DEU; DA. 1983; VOL. 88; NO 2; PP. 139-144; BIBL. 21 REF.Article

AN IMMUNOCYTOCHEMICAL SCREENING OF HUMAN-MOUSE CELL HYBRID COLONIES EXPRESSING A SPECIFIC HUMAN GENESHIMIZU Y; SHIMIZU N.1981; BIOCHEM. GENET.; ISSN 0006-2928; USA; DA. 1981; VOL. 19; NO 1-2; PP. 95-106; BIBL. 2 P.Article

A NEW CYTOGENETIC ASPECT OF POLYCYTHEMIA VERA.SHABTAI F; WEISS S; VAN DER LIJN E et al.1978; HUM. GENET.; GERM.; DA. 1978; VOL. 41; NO 3; PP. 281-287; BIBL. 21 REF.Article

FAMILIAL PERICENTRIC INVERSION 19JORDAN DK; TAYSI K; BLACKWELL NL et al.1980; J. MED. GENET.; GBR; DA. 1980; VOL. 17; NO 3; PP. 222-225; BIBL. 9 REF.Article

THE LOCUS FOR APOLIPOPROTEIN E (APO E) IS LINKED TO THE COMPLEMENT COMPONENT C3 (C3) LOCUS ON CHROMOSOME 19 IN MANOLAISEN B; TEISBERG P; GEDDE DAHL T JR et al.1982; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1982; VOL. 62; NO 3; PP. 233-236; BIBL. 15 REF.Article

BALANCED FAMILIAL TRANSLOCATION T(5;19) (Q12; P OR Q11) WITH PHENOTYPICAL ABNORMALITIES IN A GIRL. = TRANSLOCATION FAMILIALE BALANCEE T(5;19) (Q12; P OU Q11) AVEC ANOMALIES PHENOTYPIQUES CHEZ UNE FILLESTOLL C; LEVY JM; CHAMPY M et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 27; NO 3; PP. 263-267; BIBL. 4 REF.Article

ASSIGNMENT OF THE STRUCTURAL GENE FOR THE THIRD COMPONENT OF HUMAN COMPLEMENT TO CHROMOSOME 19WHITEHEAD AS; SOLOMON E; CHAMBERS S et al.1982; PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA. BIOLOGICAL SCIENCES; ISSN 0273-1134; USA; DA. 1982; VOL. 79; NO 16; PP. 5021-5025; BIBL. 42 REF.Article

MOSAIC TRISOMY 19 SYNDROMECHEN H; YU CW; WOOD MJ et al.1981; ANN. GENET.; FRA; DA. 1981; VOL. 24; NO 1; PP. 32-33; ABS. FRE; BIBL. 2 REF.Article

The DNA sequence and biology of human chromosome 19GRIMWOOD, Jane; GORDON, Laurie A; AERTS, Andrea et al.Nature (London). 2004, Vol 428, Num 6982, pp 529-535, issn 0028-0836, 7 p.Article

Assignment of the human lens fiber cell MP19 gene (LIM2) to chromosome 19q13.4, and adjacent to ETFBLIEUALLEN, K; CHRITENSEN, M; BRANDRIFF, B et al.Somatic cell and molecular genetics. 1994, Vol 20, Num 1, pp 67-69, issn 0740-7750Article

A model system for the analysis of gene exclusion: cystic fibrosis and chromosome 19WAINWRIGHT, B; FARRALL, M; WATSON, E et al.Journal of medical genetics. 1986, Vol 23, Num 5, pp 417-420, issn 0022-2593Article

Identification of novel human kallikrein-like genes on chromosome 19q13.3-q13.4YOUSEF, G. M; LUO, L.-Y; DIAMANDIS, E. P et al.Anticancer research. 1999, Vol 19, Num 4B, pp 2843-2852, issn 0250-7005Article

Assignment of the coding sequence for carcinoembryonic antigen (CEA) and normal cross-reacting antigen (NCA) to human chromosome 19q13WILLCOCKS, T. C; CRAIG, S. P; CRAIG, I. W et al.Annals of human genetics. 1989, Vol 53, Num 2, pp 141-148, issn 0003-4800, 8 p.Article

Mosaicism for ring 19: a case reportSYBERT, V. P; BRADLEY, C. M; SALK, D et al.Clinical genetics. 1988, Vol 34, Num 6, pp 382-385, issn 0009-9163Article

The physical map of chromosome arm 19q : some new assignments, confirmations and re-assessmentsBROOK, J. D; KNIGHT, S. J. L; SCHONK, D et al.Human genetics. 1991, Vol 87, Num 1, pp 65-72, issn 0340-6717Article

The eukaryotic cofactor for the human immunodeficiency virus type 1 (HIV-1) Rev protein, eIF-5A, maps to chromosome 17p12-p13 : three eIF-5A speudogenes map to 10q23.3, 17q25, and 19q13.2STEINKASSERER, A; JONES, T; SHEER, D et al.Genomics (San Diego, Calif.). 1995, Vol 25, Num 3, pp 749-752, issn 0888-7543Article

Dual localization of the human gene encoding hnRNP I/PTB protein to chromosomes 19p13.3 and 14q23DELLA VALLE, V; LE CONIAT, M; SOULARD, M et al.Human genetics. 1996, Vol 98, Num 2, pp 210-213, issn 0340-6717Article