DEPISTAGE PRENATAL DU SYNDROME DU CRI DU CHAT CHEZ LES MERES PORTEUSES DE TRANSLOCATIONS BALANCEES (5P-; 18P+)ZOLOTUKHINA TV; BUTOMO IV; ROZOVSKIJ IS et al.1981; GENETIKA; ISSN 0016-6758; SUN; DA. 1981; VOL. 17; NO 7; PP. 1304-1308; H.T. 2; ABS. ENG; BIBL. 22 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

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

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

TRISOMY 16Q21 -> QTERGARAU A; CRISPONI G; PERETTI D et al.1980; HUM. GENET.; DEU; DA. 1980; VOL. 53; NO 2; PP. 165-167; BIBL. 11 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

MULTIPLE CONGENITAL ANOMALIES-MENTAL RETARDATION (MCA/MR) SYNDROME DUE TO PARTIAL 1Q DUPLICATION AND POSSIBLE 18P DELECTION: A STUDY OF FOUR INDIVIDUALS IN TWO FAMILIESLIBERFARB RM; BREG WR; ATKINS L et al.1979; AMER. J. MED. GENET.; USA; DA. 1979; VOL. 4; NO 1; PP. 27-37; BIBL. 13 REF.Article

PARTIAL TRISOMY 12 Q ASSOCIATED WITH A FAMILIAL TRANSLOCATIONHEMMING L; BROWN R.1979; CLIN. GENET.; DNK; DA. 1979; VOL. 16; NO 1; PP. 25-28; BIBL. 4 REF.Article

PARTIAL TRISOMY 4 Q: TWO CASES RESULTING FROM A FAMILIAL TRANSLOCATION T(4;18)(Q27:P11)BONFANTE A; STELLA M; ROSSI G et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 52; NO 1; PP. 85-90; BIBL. 19 REF.Article

TRANSLOCATION 46XY, T(17;18)(Q25;Q21) IN A MENTALLY RETARDED BOY WITH PROGRESSIVE EYE ABNORMALITIESSMITH A; CARADUS V; HENRY JG et al.1979; CLIN. GENET.; DNK; DA. 1979; VOL. 16; NO 3; PP. 156-162; BIBL. 13 REF.Article

CYTOGENETIC AND ENDOCRINE FINDINGS IN A FEMALE WITH 45,X,T(Y;18) (P11;P11)CASSORLA FG; EMANUEL BS; PARKS JS et al.1981; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1981; VOL. 19; NO 5; PP. 312-320; BIBL. 13 REF.Article

REPLY TO THE LETTER OF PRIETO ET AL. CONCERNING OUR PAPER ON A CASE OF 13Q; 18Q TRANSLOCATIONNAKAGOME Y; SUZUKI Y.1980; HUM. GENET.; DEU; DA. 1980; VOL. 53; NO 2; PP. 283; BIBL. 3 REF.Article

TRISOMY 18Q:46,XX,13Q+,T(13;18)(Q32;Q11) IN A NEWBORN ASSOCIATED WITH MULTIPLE CONGENITAL ANOMALIES DUE TO PATERNAL RECIPROCAL TRANSLOCATION, 46,XY,-13,+DER(13), T(13;18)-(Q32;Q11)KRISHNA MURTHY DS; PATEL ZM; AMBANI LM et al.1980; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1980; VOL. 18; NO 4; PP. 233-238; BIBL. 21 REF.Article

CONTRIBUTION A L'ETUDE DE LA TRISOMIE 18 PARTIELLE: A PROPOS D'UN CAS PERSONNELPULVERY ANNICK.1979; ; FRA; DA. 1979; 62; 70 P.: ILL.; 29 CM; BIBL. 75 REF.; TH.: MED./CLERMONT FERRAND 1/1979Thesis

A CASE OF EDWARD'S SYNDROME WITH PSEUDODICENTRIC ISOCHROMOSOME 18: 46,XY,I DIC(18) (P11:P11)FIORETTI G; STABILE M; PAGANO L et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 2; PP. 116-118; ABS. FRE; BIBL. 13 REF.Article

PARTIELLE TRISOMIE 18 (TRISOMIE 18 P) ALS FOLGE EINER FAMILIAEREN BALANCIERTEN TRANSLOKATION T(14;18) = TRISOMIE 18 PARTIELLES (TRISOMIE 18 P) DUE A UNE TRANSLOCATION FAMILIALE BALANCEE T(14;18)MEINECKE P; KOSKE WESTPHAL T.1981; KLIN. PAEDIATR.; ISSN 0300-8630; DEU; DA. 1981; VOL. 193; NO 6; PP. 433-438; ABS. ENG; BIBL. 24 REF.Article

DISTAL 18Q DELETION WITHOUT CLINICAL FINDINGS OF 18Q-SYNDROMEQAZI QH; MADAHAR C; ALVI S et al.1980; ANN. GENET.; FRA; DA. 1980; VOL. 23; NO 1; PP. 60-62; ABS. FRE; BIBL. 6 REF.Article

PRENATAL DIAGNOSIS OF A DE NOVO RECIPROCAL TRANSLOCATION 46, XX, T(1;18) (P22; Q23)BOVICELLI L; ORSINI LF; RIZZO N et al.1980; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1980; VOL. 18; NO 6; PP. 434-435; BIBL. 4 REF.Article

TRISOMIE PARTIELLE 18(PTER->Q122) D'ORIGINE MATERNELLEJAFFRAY JY; GENEIX A; GOUMY P et al.1980; ANN. GENET.; FRA; DA. 1980; VOL. 23; NO 4; PP. 224-227; ABS. ENG; BIBL. 8 REF.Article

OBSERVATION FAMILIALE DE TRISOMIE PARTIELLE DU 6 ET MONOSOMIE PARTIELLE 18Q PROBABLE PAR TRANSLOCATION PARENTALED'EMMA C; CRIPPA L; DELOZIER C et al.1982; J. GENET. HUM.; ISSN 0021-7743; CHE; DA. 1982; VOL. 30; NO 1; PP. 39-50; ABS. ENG; BIBL. 7 REF.Article

A MALFORMED BABY WITH TWO SEPARATE DE NOVO TRANSLOCATIONSCHEWINGS WE; COCKS TP; GARDNER RJM et al.1982; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1982; VOL. 19; NO 1; PP. 70-71; BIBL. 6 REF.Article

MOSAICISME DU SYNDROME 18Q - PAR TRANSLOCATIONBADALYAN LO; DEMENT'EVA GM; MALYGINA NA et al.1981; GENETIKA; ISSN 0016-6758; SUN; DA. 1981; VOL. 17; NO 10; PP. 1867-1871; ABS. ENG; BIBL. 11 REF.Article

SUCCESSIVE SPONTANEOUS ABORTIONS ASSOCIATED WITH A TRANSLOCATION T(7Q+; 18Q-)ROSSI R; STELLA M; BONFANTE A et al.1979; CARYOLOGIA; ITA; DA. 1979 PUBL. 1980; VOL. 32; NO 4; PP. 449-454; BIBL. 18 REF.Article

Y-AUTOSOME TRANSLOCATION, GONADAL DYSGENESIS, AND GONADOBLASTOMAKHODR GS; CADENA GD; ONG TC et al.1979; AMER. J. DIS. CHILD.; USA; DA. 1979; VOL. 133; NO 3; PP. 277-282; BIBL. 23 REF.Article

A (7; 18) TRANSLOCATION, 46, XY. REPOSITERY IDENTIFICATION NO. GM-657PUNNETT HH; KISTENMACHER ML; MILLER RC et al.1979; CYTOGENET. CELL GENET.; CHE; DA. 1979; VOL. 24; NO 2; PP. 126Article