The 11q; 22q translocation: a collaborative study of 20 new cases and analysis of 110 familiesISELIUS, L; LINDSTEN, J; DUTRILLAUX, B et al.Human genetics. 1983, Vol 64, Num 4, pp 343-355, issn 0340-6717Article

A NOTE ON A PATIENT WITH A RING-22 CHROMOSOME IDENTIFIED BY BANDINGSTEWART A; RICHARDS BW.1976; J. MENTAL DEFIC. RES.; G.B.; DA. 1976; VOL. 20; NO 2; PP. 95-98; BIBL. 2 REF.Article

A(13; 22) TRANSLOCATION, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO. GM-627KIM HJ; HIRSCHHORN K; HSU LYF et al.1975; CYTOGENET. CELL. GENET.; SWITZ.; DA. 1975; VOL. 15; NO 6; PP. 406-407Article

PHILADELPHIA CHROMOSOME WITH T(6;22) (P25;Q12)MAMMON Z; GRINBLAT J; JOSHUA H et al.1976; NEW ENGL. J. MED.; U.S.A.; DA. 1976; VOL. 294; NO 16; PP. 827-828; BIBL. 8 REF.Article

A POSSIBLE CASE OF PARTIAL TRISOMY FOR CHROMOSOME 22: FURTHER EVIDENCE FROM GIEMSA BANDING STUDIES = UN CAS POSSIBLE DE TRISOMIE PARTIELLE DU CHROMOSOME 22: NOUVEAUX ARGUMENTS D'APRES L'ETUDE DES COLORATIONS EN BANDE PAR LE GIEMSASANDS ME.1974; J. MENTAL DEFIC. RES.; G.B.; DA. 1974; VOL. 18; NO 4; PP. 327-330; BIBL. 2 REF.Article

Chiasma-derived genetic lengths and recombination fractions: a reciprocal translocation 46,XY,t(1; 22)(q32; q13)PALMER, R. W; HULTEN, M. A.Annals of human genetics. 1983, Vol 47, Num 4, pp 299-310, issn 0003-4800Article

A (13;22) ROBERTSONIAN TRANSLOCATION, 45 CHROMOSOMES. REPOSITORY IDENTIFICATION NO. GM-392ALFI O; MILLER RC; GREENE AE et al.1975; CYTOGENET. CELL GENET.; SWITZ.; DA. 1975; VOL. 15; NO 1; PP. 55-56Article

THREE GENERATIONS AND SEVEN FAMILY MEMBERS WITH A T(21Q22Q) CHROMOSOME = CHROMOSOME T(21Q22Q) CHEZ SEPT MEMBRES D'UNE FAMILLE SUR TROIS GENERATIONSZERGOLLERN L.1974; J. MED. GENET.; G.B.; DA. 1974; VOL. 11; NO 4; PP. 379-381; BIBL. 5REF.Article

LA SINDROME R(22). = LE SYNDROME R(22)CURATOLO P; PAOLELLA A; PORRO G et al.1978; CLIN. PEDIATR.; ITAL.; DA. 1978; VOL. 60; NO 1; PP. 10-17; ABS. ANGL.; BIBL. 11 REF.Article

UNEXPECTED FINDINGS WITH THE NEW CHROMOSOME BANDING TECHNIQUES IN A PATIENT FORMERLY DIAGNOSED AS HAVING G-DELETION SYNDROME = RESULTATS INATTENDUS OBTENUS GRACE AUX NOUVELLES TECHNIQUES DE BANDES CHEZ UNE PATIENTE DIAGNOSTIQUEE INITIALEMENT COMME ATTEINTE DE SYNDROME II DE DELETION GORYE E; CRAEN M.1975; ACTA GENET. MED. GEMELLOL.; ITAL.; DA. 1975; VOL. 24; NO 1-2; PP. 75-82; ABS. ITAL. FR. ALLEM.; BIBL. 14 REF.Article

A (17; 22) TRANSLOCATION, BALANCED, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO GM-119MACINTYRE MN; HEMPEL JM; WALDEN DB et al.1975; CYTOGENET. CELL GENET.; SWITZ.; DA. 1975; VOL. 14; NO 1; PP. 80-81; BIBL. 2REF.Article

FAMILIAL 21/22 TRANSLOCATIONPAPP Z; DOLHAY B; GARDO S et al.1975; ACTA GENET. MED. GEMELLOL.; ITAL.; DA. 1975; VOL. 24; NO 1-2; PP. 69-73; ABS. ITAL. FR. ALLEM.; BIBL. 18 REF.Article

SEGREGATION OF A T(14Q22Q) CHROMOSOME IN A LARGE KINDRED = SEGREGATION D'UN CHROMOSOME T(14Q22Q) DANS UNE GRANDE FAMILLENEU RL; VALENTINE FA; GARDNER LI et al.1975; CLIN. GENET.; DENM.; DA. 1975; VOL. 8; NO 1; PP. 30-36; BIBL. 14 REF.Article

Translocation involving chromosome 22 in Ewing's sarcoma. A cytogenetic study of four fresh tumorsAURIAS, A; RIMBAUT, C; BUFFE, D et al.Cancer genetics and cytogenetics. 1984, Vol 12, Num 1, pp 21-25, issn 0165-4608Article

Familial DiGeorge syndrome and associated partial monosomy of chromosome 22GREENBERG, F; CROWDER, W. E; PASCHALL, V et al.Human genetics. 1984, Vol 65, Num 4, pp 317-319, issn 0340-6717Article

Translocation du chromosome 22 dans le sarcome d'Ewing = Translocation of chromosome 22 in Ewing sarcomaAURIAS, A; RIMBAUT, C; BUFFE, D et al.Comptes rendus des séances de l'Académie des sciences. Série 3, Sciences de la vie. 1983, Vol 296, Num 23, pp 1105-1107, issn 0249-6313Article

Cat eye syndrome owing to tetrasomy 22pter→q11WILSON, G. N; BAKER, D. L; SCHAU, J et al.Journal of medical genetics. 1984, Vol 21, Num 1, pp 60-63, issn 0022-2593Article

HUMAN INHERITED MARKER CHROMOSOME 22 SHORT-ARM ENLARGEMENT: INVESTIGATION OF RDNA GENE MULTIPLICITY, AG-BAND SIZE, AND ACROCENTRIC ASSOCIATIONBERNSTEIN R; DAWSON B; GRIFFITH J et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 58; NO 2; PP. 135-139; BIBL. 22 REF.Article

PARTIAL DUPLICATION OF THE LONG ARM OF CHROMOSOME 22 (22 Q 13) WITH COMPLETE 22 TRISOMY PHENOTYPEFRYNS JP; DE BACKER D; LEMLI L et al.1980; ACTA PAEDIATR. BELG.; BEL; DA. 1980; VOL. 33; NO 2; PP. 125-127; BIBL. 8 REF.Article

A FURTHER CASE OF A 22; 22 ROBERTSONIAN TRANSLOCATION ASSOCIATED WITH RECURRENT ABORTIONS.MAMELI M; CARDIA S; MILIA A et al.1978; HUM. GENET.; GERM.; DA. 1978; VOL. 41; NO 3; PP. 359-361; BIBL. 5 REF.Article

PHENOTYPIC CORRELATIONS IN PATIENTS WITH RING CHROMOSOME 22.HUNTER AGW; RAY M; WANG HS et al.1977; CLIN. GENET.; DENM.; DA. 1977; VOL. 12; NO 4; PP. 239-249; BIBL. 26 REF.Article

VARIABILITY OF R(22) CHROMOSOME PHENOTYPICAL EXPRESSION.DALLAPICCOLA B; BRINCHI V; CURATOLO P et al.1977; ACTA GENET. MED. GEMELLOL.; ITAL.; DA. 1977; VOL. 26; NO 3-4; PP. 287-290; BIBL. 4 REF.Article

A CASE OF RING CHROMOSOME G22.BROOKFIELD DSK; WALKER S.1976; J. MED. GENET.; G.B.; DA. 1976; VOL. 13; NO 6; PP. 530-532; BIBL. 6 REF.Article

A22/22 TRANSLOCATION CARRIER WITH RECURRENT ABORTIONS DEMONSTRATED BY A GIEMSA BANDING TECHNIQUEMAEDA T; OHNO M; SHIMADA N et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 31; NO 2; PP. 243-245; BIBL. 11 REF.Article

THE ASSOCIATION OF THE DIGEORGE ANOMALAD WITH PARTIAL MONOSOMY OF CHROMOSOME 22KELLEY RI; ZACKAI EH; EMANUEL BS et al.1982; JOURNAL OF PEDIATRICS; ISSN 0022-3476; USA; DA. 1982; VOL. 101; NO 2; PP. 197-200; BIBL. 22 REF.Article