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Results 1 to 25 of 21485

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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

Catch 22 : Microdeletion 22q11 screening in patients with congenital heart defectsVON BEUST, G; BARTMUS, D; BARTELS, I et al.Genetic counseling. 1998, Vol 9, Num 3, pp 223-227, issn 1015-8146Conference Paper

Aberrant expression of IL-22 receptor 1 and autocrine IL-22 stimulation contribute to tumorigenicity in ALK+ anaplastic large cell lymphomaDIEN BARD, J; GELEBART, P; ANAND, M et al.Leukemia. 2008, Vol 22, Num 8, pp 1595-1603, issn 0887-6924, 9 p.Article

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

Unusual segregation of constitutional 11q;22q translocation may be explained by crossover in interchange segment, followed by 3 : 1 segregation at meiosis ILINDENBAUM, R. H.Human genetics. 1990, Vol 85, Num 1, issn 0340-6717, p. 143Article

Recurrent t(11;22) breakpoint mapping by chromosome flow sorting and spot-blot hybridizationDELATTRE, O; GRUNWALD, M; BERNARD, A et al.Human genetics. 1988, Vol 78, Num 2, pp 140-143, issn 0340-6717Conference Paper

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

A 21 years follow-up of a girl patient with a pseudodicentric bisatellited chromosome 22 associated with partial trisomy 22pter → 22ql2.1 : Clinical, cytogenetic and molecular observationsVAGLIO, Alicia; MILUNSKY, Aubrey; HUANG, Xin-Li et al.European journal of medical genetics. 2008, Vol 51, Num 4, pp 332-342, issn 1769-7212, 11 p.Article

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

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

Five new subjects with ring chromosome 22ISHMAEL, H. A; CATALDI, D; BEGLEITER, M. L et al.Clinical genetics. 2003, Vol 63, Num 5, pp 410-414, issn 0009-9163, 5 p.Article

CHRONIC MYELOGENOUS LEUKEMIA WITH TRANSLOCATIONS (3Q-; 9Q+) AND (17Q-; 22Q+). POSSIBLE CRUCIAL CYTOGENETIC EVENTS IN THE GENESES OF CMLOSHIMURA M; OHYASHIKI K; VEHARA M et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 57; NO 1; PP. 48-51; BIBL. 21 REF.Article

Masked philadelphia chromosome resulting from a t(X; 22) in chronic myeloid leukemiaBARBATA, G; CARBONE, P; GIGLIO, M. C et al.Cancer genetics and cytogenetics. 1988, Vol 30, Num 2, pp 333-336, issn 0165-4608Article

Nucleotide sequence of both reciprocal translocation junction regions in a patient with Ph positive acute lymphoblastic leukaemia, with a breakpoint within the first intron of the BCR geneVAN DER FELTZ, M. J. M; SHIVJI, M. K. K; HEISTERKAMP, N et al.Nucleic acids research. 1989, Vol 17, Num 1, pp 1-10, issn 0305-1048Article

Prenatal diagnosis of jumping translocation involving chromosome 22 with ultrasonographic findingsASLAN, Halil; KARAMAN, Birsen; YILDIRIM, Gokhan et al.Prenatal diagnosis. 2005, Vol 25, Num 11, pp 1024-1027, issn 0197-3851, 4 p.Article

Molecular and phenotypic characterization of ring chromosome 22JEFFRIES, Aaron R; CURRAN, Sarah; ELMSLIE, Frances et al.American journal of medical genetics. 2005, Vol 137A, Num 2, pp 139-147, issn 0148-7299, 9 p.Article

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

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

In situ hybridization and translocation breakpoint mapping. II: Two unusual T(21; 22) translocationsCANNIZZARO, L. A; ARONSO, M. M; EMANUEL, B. S et al.Cytogenetics and cell genetics. 1985, Vol 39, Num 3, pp 173-178, issn 0301-0171Article

Cytogenetic heterogeneity in blast crisis (BC) of chronic myelogenous leukemia (CML)ABRAMSON, J; VERMA, R. S; SCHWARTZ, J et al.Blut. 1985, Vol 51, Num 5, pp 361-363, issn 0006-5242Article

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

UNSTABLE FAMILIAL TRANSLOCATIONS: A T(11;22) MAT INHERITED AS A T(11;15)TOMKINS DJ.1981; AM. J. HUM. GENET.; ISSN 0002-9297; USA; DA. 1981; VOL. 33; NO 5; PP. 745-751; BIBL. 24 REF.Article

9;22;15 COMPLEX TRANSLOCATION IN PH1 CHROMOSOME POSITIVE CML REVEALED BY GIEMSA-11 PROCEDURE IN APPARENT LYMPHOID CELLS OF BLASTIC CRISISHAYS T; MORSE HG; ROBINSON A et al.1981; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1981; VOL. 4; NO 4; PP. 283-292; BIBL. 16 REF.Article

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