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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

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

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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

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

A BALANCED TRANSLOCATION (17,22) AND A PERICENTRIC INVERSION OF CHROMOSOME 5: REPOSITORY IDENTIFICATION NO. GM3196TESTA JR; ROWLEY JD; HAWKINS C et al.1980; CYTOGENET. CELL GENET.; CHE; DA. 1980; VOL. 27; NO 4; PP. 270Article

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

KARYOTYPE EVOLUTION IN A CASE OF CHRONIC MYELOGENOUS LEUKEMIA WITH AN UNUSUAL PHILADELPHIA CHROMOSOME TRANSLOCATION, T(4;22), AND AN ADDITIONAL TRANSLOCATION, T(3;5)SESSAREGO M; BIANCHI SCARRA GL; AJMAR F et al.1981; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1981; VOL. 3; NO 1; PP. 47-53; BIBL. 24 REF.Article

THE IDENTIFICATION OF Y CHROMOSOME TRANSLOCATIONS FOLLOWING DISTAMYCIN A TREATMENTCOHEN MM; FREDERICK RW; BALKIN NE et al.1981; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1981; VOL. 19; NO 5; PP. 335-342; BIBL. 2 P.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

TERTIARY TRISOMY (22Q11Q),47,+DER(22), T(11;22)BIEDERMAN BM; LIN CC; LOWRY RB et al.1980; HUM. GENET.; DEU; DA. 1980; VOL. 53; NO 2; PP. 173-177; BIBL. 34 REF.Article

A PROPOS D'UNE NOUVELLE OBSERVATION DE TRISOMIE 11G SECONDAIRE A UNE TRANSLOCATION MATERNELLE T(11;22) (G23.1;G11.1)CHAUVEAU P; GRUCHY D; HEROUIN C et al.1980; ANN. GENET.; FRA; DA. 1980; VOL. 23; NO 4; PP. 213-215; ABS. ENG; BIBL. 14 REF.Article

TRANSLOCATIONS T (2;8) ET T (8;22) DANS DES LIGNEES CELLULAIRES CONTINUES DE LYMPHOMES DE BURKITT AFRICAINBERNHEIM A; BERGER R; LENOIR G et al.1980; C. R. HEBD. SEANCES ACAD. SCI., D; ISSN 0567-655X; FRA; DA. 1980; VOL. 291; NO 2; PP. 237-239; ABS. ENG; BIBL. 12 REF.Article

A NEW TRANSLOCATION IN BURKITT'S TUMOR CELLSBERGER R; BERNHEIM A; FLANDRIN G et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 53; NO 1; PP. 111-112; BIBL. 4 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

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

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

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