TANDEM TRANSLOCATION T(14;14) IN ISOLATED AND CLONAL CELLS IN ATAXIA TELANGIECTASIA ARE DIFFERENTAURIAS A; DUTRILLAUX B; GRISCELLI C et al.1983; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1983; VOL. 63; NO 4; PP. 320-322; BIBL. 11 REF.Article

SEZARY SYNDROME WITH A 14:14 (Q 12: Q 31) TRANSLOCATIONSHAH REDDY I; MAYEDA K; MIRCHANDANI I et al.1982; CANCER; ISSN 0008-543X; USA; DA. 1982; VOL. 49; NO 1; PP. 75-79; BIBL. 31 REF.Article

UNUSUAL 13/13 TRANSLOCATION AND 13 TRISOMY PHENOTYPEFRYNS JP; KLECZKOWSKA A; KUBIEN E et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 2; PP. 113-115; ABS. FRE; BIBL. 5 REF.Article

A SEVERELY RETARDED MALE WITH DELETION OF CHROMOSOME 15(PTER->Q13) AND 10(Q26->QTER)SMITH A; DEN DULK G.1982; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1982; VOL. 19; NO 1; PP. 77; BIBL. 3 REF.Article

FAMILIAL 5/14 TRANSLOCATION WITH TRIPLE X AND 47,XY+14Q-LANCET M; SINDEL L; SEGAL I et al.1981; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1981; VOL. 20; NO 1; PP. 40-43; BIBL. 21 REF.Article

FAMILIAL RECIPROCAL TRANSLOCATION T(9;13) (P11;P12) INVESTIGATED BY SILVER STAINING AND IN SITU HYBRIDISATIONVARLEY JM; GOSDEN J; HULTEN M et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 59; NO 4; PP. 422-428; BIBL. 2 P.Article

KARYOTYPE-PHENOTYPE CORRELATION IN PARTIAL TRISOMY 13BONIOLI E; CRISALLI M; MONTEVERDE R et al.1981; AM. J. DIS. CHILD. (1960); ISSN 0002-922X; USA; DA. 1981; VOL. 135; NO 12; PP. 1115-1117; BIBL. 28 REF.Article

MYELOPROLIFERATIVE DISORDER IN A T(13 Q 14 Q) CARRIERKONG OO GOH; BAUMAN AW; TOWNES PL et al.1980; CANCER; USA; DA. 1980; VOL. 45; NO 2; PP. 327-329; BIBL. 17 REF.Article

TRISOMIA 13 E TRASLOCAZIONE 13-14 SEGNALAZIONE DI DUE CASI = TRISOMIE 13 ET TRANSLOCATION 13-14. PRESENTATION DE 2 CASBOTTELLI AM; BORDONI S; CRISCITO M et al.1980; MINERVA PEDIATR.; ITA; DA. 1980; VOL. 32; NO 4; PP. 255-260; ABS. ENG; BIBL. 6 REF.Article

A CASE OF 47, XY, +DER (15), T(3; 15) (P25; Q11) PAT PRESENTING AS PARTIAL 3P TRISOMY SYNDROME WITH MULTIPLE JOINT CONTRACTURESHERSH JH; GREENSTEIN RM; PERKINS JC et al.1980; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1980; VOL. 17; NO 5; PP. 396-398; BIBL. 10 REF.Article

CONCORDANT CONGENITAL MALFORMATIONS IN TWINS WITH INHERITED TRANSLOCATION: T(9P-;13Q+)SEKHON GS; TAYSI K.1979; HUM. GENET.; DEU; DA. 1979; VOL. 50; NO 3; PP. 271-276; BIBL. 4 REF.Article

INTERSTITIAL DELETION 13Q33 RESULTING FROM MATERNAL INSERTIONAL TRANSLOCATIONEMANUEL BS; ZACKAI EH; MOREAU L et al.1979; CLIN. GENET.; DNK; DA. 1979; VOL. 16; NO 5; PP. 340-346; BIBL. 22 REF.Article

SATELLITE DNA LOSS AND NUCLEOLAR ORGANISER ACTIVITY IN AN INDIVIDUAL WITH A DE NOVO CHROMOSOME 13,14 TRANSLOCATIONGOSDEN JR; GOSDEN CM; LAWRIE SS et al.1979; CLIN. GENET.; DNK; DA. 1979; VOL. 15; NO 6; PP. 518-529; BIBL. 24 REF.Article

A TDIC (5; 15) (P13; P11) CHROMOSOME SHOWING VARIATION FOR CONSTRICTION IN THE CENTROMERIC REGIONS IN A PATIENT WITH THE CRI DU CHAT SYNDROMEDEWALD GW; BOROS SJ; CONROY MM et al.1979; CYTOGENET. CELL GENET.; CHE; DA. 1979; VOL. 24; NO 1; PP. 15-26; BIBL. 22 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

POSSIBLE INACTIVATION OF PART OF CHROMOSOME 13 DUE TO 13 QXP TRANSLOCATION ASSOCIATED WITH RETINOBLASTOMAEJIMA Y; SASAKI MS; KANEKO A et al.1982; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1982; VOL. 21; NO 6; PP. 357-361; BIBL. 18 REF.Article

THE ELFIN FACE SYNDROME AND THE SHORT ARM OF CHROMOSOME 15FRYNS JP; VAN DER HAUWAERT LG; VAN DEN BERGHE H et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 3; PP. 181-182; ABS. FRE; BIBL. 11 REF.Article

TRANSLOCATION 46.X.T(Y.14) (Q122;Q111) IN A CASE OF STERILITY IN THE MALEPETIT P; UNGLIK A; FRYNS JP et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 1; PP. 63-64; ABS. FRE; BIBL. 6 REF.Article

A BOY WITH PROXIMAL TRISOMY 15 AND A MALE FOETUS WITH DISTAL TRISOMY 15 DUE TO A FAMILIAL 13P; 15Q TRANSLOCATIONANNEREN G; GUSTAVSON KH.1982; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1982; VOL. 22; NO 1; PP. 16-21; BIBL. 11 REF.Article

A COMPLEX CHROMOSOME REARRANGEMENT RESULTING IN TRISOMY 15Q22->QTERHOWARD PEEBLES PN; SCARBROUGH PR; SHARPE J et al.1982; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1982; VOL. 19; NO 3; PP. 224-227; BIBL. 5 REF.Article

PROXIMAL TRISOMY 13. A FAMILY WITH BALANCED RECIPROCAL TRANSLOCATION T(8;13) IN SEVEN MEMBERS AND ROBERTSONIAN TRANSLOCATION T(13;14) IN THREE MEMBERSGILGENKRANTZ S; DEFECHE C; STEHLIN S et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 58; NO 4; PP. 436-440; BIBL. 25 REF.Article

FURTHER OBSERVATIONS ON A 13QXP TRANSLOCATION ASSOCIATED WITH RETINOBLASTOMANICHOLS WW; MILLER RC; SOBEL M et al.1980; AMER. J. OPHTHALMOL.; USA; DA. 1980; VOL. 89; NO 5; PP. 621-627; BIBL. 29 REF.Article

PARTIAL TRISOMY 13 WITH PHENOTYPE OF PATAU SYNDROME DUE TO MATERNAL RECIPROCAL TRANSLOCATION T(6;13)(Q25;Q13)PETIT P; FRYNS JP; VAN DEN BERGHE H et al.1980; ANN. GENET.; FRA; DA. 1980; VOL. 23; NO 1; PP. 57-59; ABS. FRE; BIBL. 13 REF.Article

CHROMOSOME ANALYSIS IN TWO UNUSUAL MALIGNANT BLOOD DISORDERS PRESUMABLY INDUCED BY BENZENEVAN DER BERGHE H; LOUWAGIE A; BROECKAERT VAN ORSHOVEN A et al.1979; BLOOD; USA; DA. 1979; VOL. 53; NO 4; PP. 558-566; BIBL. 18 REF.Article

CHROMOSOMES IN RETINOBLASTOMA PATIENTSDAVISON EV; GIBBONS B; AHERNE GES et al.1979; CLIN. GENET.; DNK; DA. 1979; VOL. 15; NO 6; PP. 505-508; BIBL. 17 REF.Article