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NOR ACTIVITY IN TWO FAMILIES WITH BALANCED D; D TRANSLOCATIONS AND NUMEROUS CONSECUTIVE MISCARRIAGESGAHMBERG N; PAJUNEN L; DE LA CHAPELLE A et al.1980; HEREDITAS; SWE; DA. 1980; VOL. 92; NO 2; PP. 217-221; BIBL. 31 REF.Article

CHROMOSOMES IN THE CORNELIA DE LANGE SYNDROMEBECK B; MIKKELSEN M.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 59; NO 4; PP. 271-276; BIBL. 38 REF.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

REPRODUCTIVE RISK OF T(13Q 14Q) CARRIERS: CASE REPORT AND REVIEWHARRIS DJ; HANKINS L; BEGLEITER ML et al.1979; AMER. J. MED. GENET.; USA; DA. 1979; VOL. 3; NO 2; PP. 175-181; BIBL. 30 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

TRISOMY 20PTER -> Q11 IN A MALFORMED BOY FROM A T(13;20)(P11;Q11) TRANSLOCATION-CARRIER MOTHERSCHINZEL A.1980; HUM. GENET.; DEU; DA. 1980; VOL. 53; NO 2; PP. 169-172; BIBL. 9 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

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 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

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

CLINICAL MANIFESTATIONS OF FAMILIAL 13, 18 TRANSLOCATIONBLATTNER WA; KISTENMACHER ML; SHIEN TSAI et al.1980; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1980; VOL. 17; NO 5; PP. 373-379; BIBL. 27 REF.Article

CYTOGENETIC STUDIES IN AN ACUTE LEUKEMIA PATIENT FOLLOWING CEREBELLAR ASTROCYTOMANORA A; HEIDEMAN R; PEAKMAN D et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 50; NO 2; PP. 157-161; BIBL. 12 REF.Article

HIGH RATE OF DETECTION OF 13Q14 DELETION MOSAICISM AMONG RETINOBLASTOMA PATIENTS (USING MORE EXTENSIVE METHODS)MOTEGI T.1982; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1982; VOL. 61; NO 2; PP. 95-97; BIBL. 9 REF.Article

TROUBLES PHENOTYPIQUES LORS DE LA TRANSLOCATION RECIPROQUE EQUILIBREE: CARYOTYPE 46XYRCP(13;21) (Q22:Q22)BADALYAN LO; MALYGINA NA; GOZMAN TV et al.1982; CITOL. GENET. (KIEV); ISSN 0564-3783; UKR; DA. 1982; VOL. 16; NO 2; PP. 17-21; ABS. ENG; BIBL. 9 REF.Article

NORS AND SATELLITE ASSOCIATIONS IN A FAMILY WITH 13/14 TRANSLOCATIONNIKOLIS J; KEKIC V; DIKLIC V et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 59; NO 4; PP. 342-344; BIBL. 25 REF.Article

PARTIAL TRISOMY 13 (Q21.3->QTER) RESULTING FROM A MATERNAL TRANSLOCATION T(13; 21)PANGALOS C; COUTURIER J.1981; ANN. GENET.; FRA; DA. 1981; VOL. 24; NO 3; PP. 179-181; ABS. FRE; BIBL. 6 REF.Article

PARTIAL TRISOMY 13(Q14->QTER) DUE TO A FAMILIAL TRANSLOCATION T(13;18) (Q14;Q23)STEINBACH P.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 58; NO 4; PP. 444Article

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

A DERIVATIVE CHROMOSOME 13 PAT IN A SUBJECT WITH MULTIPLE CONGENITAL ABNORMALITIES. REPOSITORY IDENTIFICATION NO GM-1224KOHN G; COHEN MM; ARONSON MM et al.1979; CYTOGENET. CELL. GENET.; CHE; DA. 1979; VOL. 24; NO 3; PP. 197; BIBL. 1 REF.Article

Translocation t(13; 14) in nine generations with a case of translocation homozygosityEKLUND, A; SIMOLA, K. O. J; RYYNANEN, M et al.Clinical genetics. 1988, Vol 33, Num 2, pp 83-86, issn 0009-9163Article

Measurements of plasma X-radiation by the photoelectron methodGOTT, Y. V; SHURYGIN, V. A.Nuclear fusion. 1988, Vol 28, Num 4, pp 543-548, issn 0029-5515Article

Trisomy 13 in the child of two carriers of a 13/15 translocationMORI, M. A; HUERTAS, H; PINEL, I et al.American journal of medical genetics. 1985, Vol 20, Num 1, pp 17-20, issn 0148-7299Article

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

Union de deux porteurs de translocation équilibrée. Etude familiale sur trois générations = A union of two balanced translocation carriers. Family study over three generationsGILGENKRANTZ, S; GREGOIRE, M.-J; CHERY, M et al.Annales de génétique (Paris). 1985, Vol 28, Num 3, pp 164-166, issn 0003-3995Article