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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

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

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

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

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

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

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

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

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

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

Mosaic trisomy 22: five new cases with variable outcomes. Implications for genetic counselling and clinical managementLECLERCQ, Sandrine; BARON, Xavier; JACQUEMONT, Marie-Line et al.Prenatal diagnosis. 2010, Vol 30, Num 2, pp 168-172, issn 0197-3851, 5 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

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

Arrangement of chromosome 11 and 22 territories, EWSR1 and FLI1 genes, and other genetic elements of these chromosomes in human lymphocytes and Ewing sarcoma cellsTASLEROVA, Renata; KOZUBEK, Stanislav; LUKASOVA, Emilie et al.Human genetics. 2003, Vol 112, Num 2, pp 143-155, issn 0340-6717, 13 p.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

Bilateraler kolobomatöser Mikrophthalmus mit orbitalen Riesnezysten bei inkompletter Tetrasomie 22 = Bilateral colobomatous microphthalmos with orbital cysts and incomplete tetrasomy 22LANGE, W; ROCHELS, R; OTTE, J et al.Klinische Monatsblätter für Augenheilkunde. 1992, Vol 200, Num 6, pp 671-673, issn 0023-2165Article

Ring chromosome 22 : a case reportSEVERIEN, C; FELIX, S; BARTHOLOME, K et al.Klinische Pädiatrie. 1991, Vol 203, Num 6, pp 467-469, issn 0300-8630Article

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

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