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

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

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

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

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

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

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

Paracentric inversion of chromosome 19 in three generationsPHELAN, M. C; SCHROER, R. J; KRUG, E. F et al.American journal of medical genetics. 1989, Vol 34, Num 4, pp 525-527, issn 0148-7299Article

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

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

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

Involvement of 19q13 in follicular thyroid adenomaDAL CHIN, P; SNEYERS, W; SAYED ALY, M et al.Cancer genetics and cytogenetics. 1992, Vol 60, Num 1, pp 99-101, issn 0165-4608Article

Translocation t (11:19) (q21; p13.1) as the sole chromosome abnormality in a cystadenolymphoma (Warthin's tumor) of the parotid glandBULLERDIEK, J; HAUBRICH, J; MEYER, K et al.Cancer genetics and cytogenetics. 1988, Vol 35, Num 1, pp 129-132, issn 0165-4608, 4 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

TRISOMY 19QLANGE M; ALFI OS.1976; ANN. GENET.; FR.; DA. 1976; VOL. 19; NO 1; PP. 17-21; ABS. FR.; BIBL. 11 REF.Article

Intermediate lymphocytic lymphoma with both t(14;19)(p32.3;q13.1) and t(3;22)(q27;q11.2)NAKAGAWA, M; SUGIYAMA, H; OGAWA, H et al.Cancer genetics and cytogenetics. 1995, Vol 79, Num 1, pp 89-91, issn 0165-4608Article

A new variant translocation of t(15;17) in a patient with acute promyelocytic leukemia (M3) : t(15;19;17)(q22;p13;q12)SAITOH, K; MIURA, I; MIURA, A. B et al.Cancer genetics and cytogenetics. 1998, Vol 102, Num 1, pp 15-18, issn 0165-4608Article

t(4;19)(q35;q13.1) : A recurrent change in primitive mesenchymal tumors ?RICHKIND, K. E; ROMANSKY, S. G; FINKLESTEIN, J. Z et al.Cancer genetics and cytogenetics. 1996, Vol 87, Num 1, pp 71-74, issn 0165-4608Article

Pericentric inversion of chromosome 19: prenatal diagnosis and genetic counsellingTHARAPEL, A. T; WARD, J. C; WIGGINS, L et al.Prenatal diagnosis. 1986, Vol 6, Num 1, pp 75-78, issn 0197-3851Article

MLL/ENL fusion in congenital acute lymphoblastic leukemia with a unique t(11;18;19)HORSTMANN, M; ARGYRIOU-TIRITA, A; BORKHARDT, A et al.Cancer genetics and cytogenetics. 1996, Vol 88, Num 2, pp 103-109, issn 0165-4608Article

FISH analyses of a newly established thyroid tumor cell line showing a t(1;19)(p35 or p36.1;q13) reveal that the breakpoint lies between 19q13.3-13.4 and 19q.13.4BELGE, G; GARCIA, E; DE JONG, P et al.Cytogenetics and cell genetics. 1995, Vol 69, Num 3-4, pp 220-222, issn 0301-0171Article

High-resolution cytogenetic characterization of telomeric associations in ring chromosome 19SAWYER, J. R; ROWE, R. A; HASSED, S. J et al.Human genetics. 1993, Vol 91, Num 1, pp 42-44, issn 0340-6717Article

Pericentric inversion of chromosome 19 in three familiesD'ALESSANDRO, E; DE MATTEIS VACCARELLA, C; LO RE, M. L et al.Human genetics. 1988, Vol 80, Num 2, pp 203-204, issn 0340-6717Article

The prenatal detection of a familial pericentric inversion of chromosome 19COUZIN, D. A; WATT, J. L; STEPHEN, G. S et al.Prenatal diagnosis. 1986, Vol 6, Num 1, pp 79-82, issn 0197-3851Article