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Results 1 to 25 of 50364

  • Page / 2015
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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

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 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

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

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

Male pseudohermaphroditism and gonadal mosaicism in a 47,XY,+22 fetusMELANIE BEAULIEU BERGERON; TRAN-THANH, Danh; FOURNET, Jean-Christophe et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 16, pp 1768-1772, issn 1552-4825, 5 p.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

IL-22 : A critical mediator in mucosal host defenseAUJLA, S. J; KOLLS, J. K.Journal of molecular medicine (Berlin. Print). 2009, Vol 87, Num 5, pp 451-454, issn 0946-2716, 4 p.Article

Double trisomie et inversion péricentrique transmise [48,XXY, +21, inv(22)] effet interchrosomique = Double trisomy and inherited pericentric inversion [48,XXY, +21, inv(22)] interchromosomal effectSAURA, R; LONGY, M; SAUTAREL, M et al.Annales de génétique (Paris). 1983, Vol 26, Num 3, pp 180-182, issn 0003-3995Article

A CASE OF TRISOMY 22 IN PONGO PYGMAEUSANDRLE M; FIEDLER W; RETT A et al.1979; CYTOGENET. CELL GENET.; CHE; DA. 1979; VOL. 24; NO 1; PP. 1-6; BIBL. 17 REF.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

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

Welche Kältemittel in der Zukunft? = Which refrigerant in the future?DOÊRING, R.Die Kälte und Klimatechnik. 1990, Vol 43, Num 9, pp 472-482, issn 0343-2246, 6 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

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

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

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

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

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

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

  • Page / 2015