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Results 1 to 25 of 20645

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Anesthesia in a patient with chromosome 11;22 translocation : a case report and literature reviewDRUM, Elizabeth T; HERLICH, Andrew; LEVINE, Bruce et al.Paediatric anaesthesia (Paris). 2005, Vol 15, Num 11, pp 985-987, issn 1155-5645, 3 p.Article

Approche moléculaire des remaniements du chromosome 22 humain observés dans des pathologies tumorales non hématologiques: cas particulier de la t(11; 22) du Sarcome = Molecular approach of human chromosome 22 rearrangements observed in non hematologic tumoral pathologies with particular interest to the t(11; 22) Ewing's sarcoma specific translocationDelattre, Olivier; Thomas, Gilles.1991, 117 p.Thesis

HABITUAL ABORTION AND TRANSLOCATION (22Q; 22Q): UNEXPECTED TRANSMISSION FROM A MOTHER TO HER PHENOTYPICALLY NORMAL DAUGHTERKIRKELS VGHJ; HUSTINX TWJ; SCHERES JMJC et al.1980; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1980; VOL. 18; NO 6; PP. 456-461; BIBL. 23 REF.Article

Loss of sodium from mung bean shoots to saline root mediaSALIM, M.Journal of agronomy and crop science (1986). 1988, Vol 160, Num 5, pp 314-318, issn 0931-2250Article

THE 11Q; 22Q TRANSLOCATION: A EUROPEAN COLLABORATIVE ANALYSIS OF 43 CASESFRACCARO M; LINDSTEN J; FORD CE et al.1980; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1980; VOL. 56; NO 1; PP. 21-51; BIBL. 1 P.Article

PARTIAL TRISOMY OF 13 (PTER->Q12) DUE TO 47, XY,+DER (13), T(13; 22) (Q12; Q13)MATMOEDJONO SJ; SPARKES RS.1979; HUM. GENET.; DEU; DA. 1979; VOL. 50; NO 3; PP. 241-246; BIBL. 19 REF.Article

Pseudoisodicentric bisatellited extra marker chromosome (tetrasomy 22pter→q11, trisomy Yqh), derived from a maternal Y/22 translocation. Association between this tetrasomy and Cat eyë phenotypical featuresGABARRON, J; GLOVER, G; JIMENEZ, A et al.Clinical genetics. 1985, Vol 28, Num 6, pp 509-515, issn 0009-9163Article

Unbalanced 3;22 Translocation With 22q11 and 3p Deletion SyndromeDUNDAR, Munis; KIRAZ, Aslihan; TASDEMIR, Sener et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 11, pp 2791-2795, issn 1552-4825, 5 p.Article

PARTIAL TRISOMY 13. THE MYTH OF NONMONGOLOID TRISOMY GPATIL SR; ZELLWEGER H.1981; CLIN. PEDIATR.; ISSN 0009-9228; USA; DA. 1981; VOL. 20; NO 8; PP. 534-536; BIBL. 15 REF.Article

The most frequent constitutional translocation in humans, the t(11;22)(q23;q11) is due to a highly specific Alu-mediated recombinationHILL, A. S; FOOT, N. J; CHAPLIN, T. L et al.Human molecular genetics (Print). 2000, Vol 9, Num 10, pp 1525-1532, issn 0964-6906Article

High resolution banding of chronic myeloid leukemia chromosomesMOHAMED, A. N; CLARKSON, B. D; CHAGANTI, R. S. K et al.Cancer genetics and cytogenetics. 1986, Vol 20, Num 3-4, pp 209-222, issn 0165-4608Article

Mosaic down's syndrome with de novo 45, XX, -21, -22, +t(21q; 22q)/46, XX, -21, +t(21q:21q) rearrangementTHARAPEL, A. T; REDHEENDRAN, R; MANKINEN, B et al.Journal of medical genetics. 1984, Vol 21, Num 5, pp 391-395, issn 0022-2593Article

UN CAS DE TRISOMIE 9 P PAR TRANSLOCATION MATERNELLE T(9,22)DELPECH DOMINIQUE.1979; ; FRA; DA. 1979; 61 P.: ILL; 30 CM; BIBL. 79 REF.; TH.: MED./NICE/1979Thesis

CONTRIBUTION A L'ETUDE DU CHROMOSOME 11 CHEZ L'HOMME. A PROPOS D'UNE OBSERVATION DE TRISOMIE 11 Q. PAR TRANSLOCATION FAMILIALEHUBERT JACQUES.sd; FRA; DA. S.D.; 143; 96 P.-7. PL.; 30 CM; BIBL. 226 REF.; TH.: MED./NANCY 1/1979Thesis

Partial monosomy 15q due to de novo t(15; 22)(q15;p11)MORI, M. A; RODRIGUEZ, L; PINEL, I et al.Annales de génétique (Paris). 1987, Vol 30, Num 4, pp 246-248, issn 0003-3995Article

Role of heterochromatin during preferential 9q;22q translocation in chronic myelogenous leukemiaVERMA, R. S; RODRIGUEZ, J; ARVIND BABU et al.Canadian journal of genetics and cytology. 1986, Vol 28, Num 6, pp 998-1002, issn 0008-4093Article

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

FAMILIAL Y-AUTOSOME TRANSLOCATION IN TWO UNRELATED GIRLSFUNDERBURK SJ; KLISAK I; SPARKES RS et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 2; PP. 119-122; ABS. FRE; BIBL. 24 REF.Article

UN CAS DE TRISOMIE 22 INCOMPLETE DUE A LA MALSEGREGATION MEIOTIQUE D'UNE TRANSLOCATION FAMILIALE 11:22PESCIA G; JOTTERAND BELLOMO M; GAIDE AC et al.1981; REV. MED. SUISSE ROMANDE; ISSN 0035-3655; CHE; DA. 1981; VOL. 101; NO 4; PP. 325-329; BIBL. 6 REF.Article

TRISOMIE PARTIELLE 11Q PAR MALSEGREGATION D'UNE TRANSLOCATION MATERNELLE T(11; 22) (P23; P11.1)PANGALOS C; COUTURIER J; BARTSOCAS C et al.1980; NOUV. PRESSE MED.; ISSN 0301-1518; FRA; DA. 1980; VOL. 9; NO 41; PP. 3065-3067; ABS. ENG; BIBL. 7 REF.Article

Additional deletion in sex-determining region of human Y chromosome resolves paradox of X,t(Y;22) femalePAGE, D. C; FISHER, E. M. C; MCGILLIVRAY, B et al.Nature (London). 1990, Vol 346, Num 6281, pp 279-281, issn 0028-0836, 3 p.Article

Trisomy 22 in a liveborn infant with multiple congenital anomaliesMCPHERSON, E; STETKA, D. G.American journal of medical genetics. 1990, Vol 36, Num 1, pp 11-14, issn 0148-7299, 4 p.Article

Myxoid chondrosarcoma with a translocation involving chromosomes 9 and 22HINRICHS, S. H; JARAMILLO, M. A; GUMERLOCK, P. H et al.Cancer genetics and cytogenetics. 1985, Vol 14, Num 3-4, pp 219-226, issn 0165-4608Article

X-inactivation patterns in lymphocytes and skin fibroblasts of three cases of X-autosome translocations with abnormal phenotypesDISTECHE, C. M; SWISSHELM, K; FORBES, S et al.Human genetics. 1984, Vol 66, Num 1, pp 71-76, issn 0340-6717Article

RED BLOOD CELL GLUTATHIONE PROXIDASE IN SIMPLE TRISOMY 21 AND TRANSLOCATION 21/22KEDZIORA J; LUKASZEWICZ R; KOTER M et al.1982; EXPERIENTIA; ISSN 0014-4754; CHE; DA. 1982; VOL. 38; NO 5; PP. 543-544; BIBL. 20 REF.Article

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