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

DiGeorge syndrome : part of CATCH 22WILSON, D. I; BURN, J; SCAMBLER, P et al.Journal of medical genetics. 1993, Vol 30, Num 10, pp 852-856, issn 0022-2593Article

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

A fertile man with tdic(Y;22): how a stable neo-X₁X₂Y sex-determining mechanism could evolve in manCALLEN, D. F; SUTHERLAND, G. R; CARTER, R. F et al.American journal of medical genetics. Supplement. 1987, Num 3, pp 151-155, issn 1040-3787Article

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

Isochromosome 22 in trisomy 22 mosaic with five cell linesGUZE, Carol; NAIGENG QIN; KELLY, Joann et al.American journal of medical genetics. 2004, Vol 124A, Num 1, pp 79-84, issn 0148-7299, 6 p.Article

MEIOTIC SEGREGATION IN FAMILIAL RECIPROCAL TRANSLOCATION T (8Q; 22Q)GOEDDE SALZ E; OESINGHAUS S; GROTE W et al.1982; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1982; VOL. 11; NO 2; PP. 241-247; BIBL. 10 REF.Article

INCOMPLETE TRISOMY 22. II. FAMILIAL TRISOMY OF THE DISTAL SEGMENT OF CHROMOSOME 22Q IN TWO BROTHERS FROM A MOTHER WITH A TRANSLOCATION, T(6; 22) (Q27; Q13)SCHINZEL A.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 56; NO 3; PP. 263-268; BIBL. 5 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 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

Erythrocytosis and complex Ph translocation 46,XY,t(9;11;22) in a patient with chronic myelogenous leukemiaKUBOTA, K; ARAI, T; SHIRAKURA, T et al.Cancer genetics and cytogenetics. 1987, Vol 24, Num 2, pp 359-362, issn 0165-4608Article

TRANSLOCATION 21Q22Q IN AN INFERTILE HUMAN MALECHANDLEY AC; HARGREAVE TB; FLETCHER JM et al.1982; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1982; VOL. 19; NO 5; PP. 366-369; BIBL. 19 REF.Article

INCOMPLETE TRISOMY 22. I: FAMILIAL 11/22 TRANSLOCATION WITH 3:1 MEIOTIC DISJUNCTION. DELINEATION OF A COMMON CLINICAL PICTURE AND REPORT OF NINE NEW CASES FROM SIX FAMILIESSCHINZEL A; SCHMID W; DER MAUR PA et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 56; NO 3; PP. 249-262; BIBL. 2 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

Homozygosity for a Y/22 chromosome translocation: t(Y; 22) (q12; p12/13)LESCHOT, N. J; VELDEN, J. V. D; MARINKOVIC-ILSEN, A et al.Clinical genetics. 1986, Vol 29, Num 3, pp 251-257, issn 0009-9163Article

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