DOUBLE 9,22 TRANSLOCATION WITH HYPERDIPLOIDY APPEARING IN BLASTIC TRANSFORMATION OF CHRONIC GRANULOCYTIC LEUKEMIAPOORNIMA RAJASEKARIAH; ILLES I; GARSON OM et al.1982; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1982; VOL. 7; NO 1; PP. 85-88; BIBL. 5 REF.Article

A SUMMARY OF CYTOGENETIC, MORPHOLOGIC, AND CLINICAL DATA ON T(8Q-; 21Q+) AND T(15Q+; 17Q-) TRANSLOCATION LEUKEMIAS IN JAPANSAKURAI M; SASAKI M; KAMADA N et al.1982; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1982; VOL. 7; NO 1; PP. 59-65; BIBL. 15 REF.Article

FETAL PHENOTYPE IN A CASE OF PARTIAL TRISOMY 21 AND PARTIAL MONOSOMY 22 DETECTED PRENATALLYMIGLIORINI AM; COCO R; DE NEGROTTI TC et al.1981; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1981; VOL. 18; NO 5; PP. 383-385; BIBL. 8 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

CHRONIC MYELOGENOUS LEUKEMIA WITH A COMPLEX TRANSLOCATIONMOHANDAS T; ANDERSON C; OKUN D et al.1980; CANCER GENET. CYTOGENET.; USA; DA. 1980; VOL. 2; NO 1; PP. 19-21; BIBL. 8 REF.Article

SITE-SPECIFIC RECIPROCAL TRANSLOCATION, T(11;22) (Q23; Q11), IN SEVERAL UNRELATED FAMILIES WITH 3:1 MEIOTIC DISJUNCTIONZACKAI EH; EMANUEL BS.1980; AMER. J. MED. GENET.; USA; DA. 1980; VOL. 7; NO 4; PP. 507-521; BIBL. 50 REF.Article

FIVE FAMILIAL CASES WITH A TRISOMY 16 P SYNDROME DUE TO TRANSLOCATIONLESCHOT NJ; DE NEF JJ; GERAEDIS JPM et al.1979; CLIN. GENET.; DNK; DA. 1979; VOL. 16; NO 3; PP. 205-214; BIBL. 5 REF.Article

PARTIAL TRISOMY OF 11 AND 22 DUE TO FAMILIAL TRANSLOCATION T(11;22)(Q23;Q11), INHERITED IN THREE GENERATIONSNAKAI H; YAMAMOTO Y; KUROKI Y et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 51; NO 3; PP. 349-355; BIBL. 12 REF.Article

DELINEATION OF ROBERTSONIAN TRANSLOCATIONS IN MAN BY MEANS OF CHROMOSOME BANDING.HILL FS JR; SUMMITT RL.1977; EUROP. J. PEDIATR.; GERM.; DA. 1977; VOL. 126; NO 4; PP. 203-209; BIBL. 20 REF.Article

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

MEIOTIC AND SYNAPTONEMAL COMPLEX STUDIES IN A 14/21 TRANSLOCATION CARRIERVIDAL F; TEMPLADO C; NAVARRO J et al.1982; INT. J. ANDROL.; ISSN 0105-6263; DNK; DA. 1982; VOL. 5; NO 1; PP. 21-26; BIBL. 17 REF.Article

MODERATE DOWN'S SYNDROME IN THREE SIBLINGS HAVING PARTIAL TRISOMY 21Q22.2->QTER AND THEREFORE NO SOD-1 EXCESSHADEBANK M; RODEWALD A.1982; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1982; VOL. 60; NO 1; PP. 74-77; BIBL. 12 REF.Article

VARIANT TRANSLOCATION IN A NON ENDEMIC CASE OF BURKITT'S LYMPHOMA: T(8;22) IN AN EPSTEIN-BARR VIRUS NEGATIVE TUMOUR AND IN A DERIVED CELL LINEBERTRAND S; BERGER R; PHILIP T et al.1981; EUR. J. CANCER; ISSN 0014-2964; GBR; DA. 1981; VOL. 17; NO 5; PP. 577-584; BIBL. 17 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

COMPLEX CHROMOSOME REARRANGEMENTS. REPORT OF A NEW CASE AND LITERATURE REVIEWPAI GS; THOMAS GH; MAHONEY W et al.1980; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1980; VOL. 18; NO 6; PP. 436-444; BIBL. 1 P.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

OMPHALOCELE AND PARTIAL TRISOMY 1Q SYNDROMECHEN H; GERSHANIK JJ; MAILHES JB et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 53; NO 1; PP. 1-4; BIBL. 27 REF.Article

TWO CHILDREN WITH PARTIAL TRISOMY FOR 7PBERRY AC; HONEYCOMBE J; MACOUN SJR et al.1979; J. MED. GENET.; GBR; DA. 1979; VOL. 16; NO 4; PP. 320-321; BIBL. 2 REF.Article

SINDROME 18P - DA TRASLOCAZIONE 18/21 = SYNDROME 18P - PAR TRANSLOCATION 18/21FERRANTE E; CHESSA L; BRUNI L et al.1979; MINERVA PEDIATR.; ITA; DA. 1979; VOL. 31; NO 8; PP. 657-664; ABS. ENG; BIBL. 2 P.Article

PARTIAL TRISOMY 7P IN TWO FAMILIES RESULTING FROM DIFFERENT BALANCED TRANSLOCATIONSMOORE CM; PFEIFFER RA; CRAIG HOLMES AP et al.1982; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1982; VOL. 21; NO 2; PP. 112-121; BIBL. 13 REF.Article

A COMPLEX REARRANGEMENT INVOLVING THREE AUTOSOMES IN A PHENOTYPICALLY NORMAL MALE PRESENTING WITH STERILITYTHOMAS IM.1982; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1982; VOL. 19; NO 5; PP. 375-377; BIBL. 21 REF.Article

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

CYTOGENETIC FOLLOW-UP OF PATIENTS WITH NONLYMPHOCYTIC LEUKEMIA. II: ACUTE NONLYMPHOCYTIC LEUKEMIAHAGEMEIJER A; KAHLEN K; ABELS J et al.1981; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1981; VOL. 3; NO 2; PP. 109-124; BIBL. 19 REF.Article

TRISOMY 6 QTERTURLEAU C; DE GROUCHY J.1981; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1981; VOL. 19; NO 3; PP. 202-206; BIBL. 9 REF.Article

OBSERVATION FAMILIALE DE TRISOMIE POUR LA PARTIE TERMINALE DU CHROMOSOME 10STOLL C; ROTH MP.1981; ARCH. FR. PEDIATR.; ISSN 0003-9764; FRA; DA. 1981; VOL. 38; NO 4; PP. 273-274; ABS. ENG; BIBL. 5 REF.Article