PARTIAL TRISOMY OF CHROMOSOME 15.HOWARD PEEBLES PN; YARBROUGH K; STODDARD GR et al.1977; AMER. J. MENTAL DEFIC.; U.S.A.; DA. 1977; VOL. 81; NO 6; PP. 606-609; BIBL. 15 REF.Article

TRISOMY 8P DUE TO THE 3:1 SEGREGATION OF THE BALANCED TRANSLOCATION T(8;15) MATLAZJUK GI; LURIE IW; USOVA YI et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 46; NO 3; PP. 335-339; BIBL. 15 REF.Article

FAMILIAL PARTIAL TRISOMY 15.POWER MM; BARRY RG; CANNON DE et al.1977; ANN. GENET.; FR.; DA. 1977; VOL. 20; NO 3; PP. 159-165; ABS. FR.; BIBL. 22 REF.Article

SYNDROME +12P. CASE REPORT AND REVIEW.TENCONI R; PIOVAN E; PRETO A et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 39; NO 1; PP. 97-101; BIBL. 10 REF.Article

PARTIAL 2P TRISOMY (P21->PTER) IN TWO SIBLINGS OF A FAMILY WITH A 2P-: 15Q+TRANSLOCATION.ARMENDARES S; SALAMANCA GOMEZ F.1978; CLIN. GENET.; DENM.; DA. 1978; VOL. 13; NO 1; PP. 17-24; BIBL. 5 REF.Article

KARYOTYP-PHENOTYP-KORRELATION BEI EINEM 46, XDEL (X) (P22)-BEFUND = CORRELATION PHENOTYPE CARYOTYPE DANS UN DIAGNOSTIC 46, XDEL (X) (P22)BARTSCH SANDHOFF M; TERINDE R; WIEGELMANN W et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 31; NO 3; PP. 263-270; ABS. ANGL.; BIBL. 10 REF.Article

THE 9P-DELETION SYNDROME. REPORT OF A PATIENT WITH A 46,XX,9P-CONSTITUTION DUE TO A PATERNAL T(9P-;15Q+) TRANSLOCATIONORYE E; VERHAAREN H; VAN DEN BOAERT VAN HEESVELDE AM et al.1975; CLIN. GENET.; DENM.; DA. 1975; VOL. 8; NO 5; PP. 349-357; BIBL. 8 REF.Article

THE PRADER-WILLI SYNDROME WITH A 15/15 TRANSLOCATION. CASE REPORT AND REVIEW OF THE LITERATUREHAWKEY CJ; SMITHIES A.1976; J. MED. GENET.; G.B.; DA. 1976; VOL. 13; NO 2; PP. 152-157; BIBL. 32 REF.Article

TRISOMY 9P IN A PATIENT WITH A DE NOVO 9/15 TRANSLOCATION = TRISOMIE 9P CHEZ UNE MALADE PORTEUSE D'UNE TRANSLOCATION 9/15 DE NOVOJACOBSEN P; HOBOLTH N; MIKKELSEN M et al.1975; CLIN. GENET.; DENM.; DA. 1975; VOL. 7; NO 4; PP. 317-324; BIBL. 14REF.Article

CRI-DU-CHAT SYNDROME IN A CHILD WITH A 5/15 TRANSLOCATION AND INTERSTITIAL CENTROMETRIC HETEROCHROMATINGEBAUER HJ; STUMPF B; HANSMANN I et al.1978; CLIN. GENET.; DNK; DA. 1978; VOL. 14; NO 6; PP. 345-350; BIBL. 30 REF.Article

ORIGIN OF A SMALL METACENTRIC CHROMOSOME: FAMILIAL AND CYTOGENETIC EVIDENCE = ORIGINE D'UN PETIT CHROMOSOME METACENTRIQUE: PREUVE FAMILIALE CYTOGENETIQUETAYLOR KM; WOLFINGER HL; BROWN MG et al.1975; CLIN. GENET.; DENM.; DA. 1975; VOL. 8; NO 5; PP. 364-369; BIBL. 11 REF.Article

REPORT OF A TRISOMY 8P INFANT WITH CARNIER FATHERFUNDERBURK SJ; BARRETT CT; KLISAK I et al.1978; ANN. GENET.; FRA; DA. 1978; VOL. 21; NO 4; PP. 219-222; ABS. FRE; BIBL. 12 REF.Article

ETUDE CYTOGENETIQUE DE LA MALADIE DU CRI DU CHAT. A PROPOS D'UNE FAMILLE OU TROIS ENFANTS SONT ATTEINTS DE L'AFFECTION ET UN DE SA RECIPROQUEBOUVIER G.1974; LYON; ASSOC. CORP. ETUD. MED. LYON; DA. 1974; PP. 1-62; BIBL. 19P.; (THESE DOCT. MED.; CLAUDE-BERNARD LYON)Thesis

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

A PROPOS D'UN CAS DE TRISOMIE 15 PARTIELLE.SAME EKOBO VOISIN C.1977; ; S.L.; DA. 1977; PP. 1-98; H.T. 12; BIBL. 19 P.; (THESE DOCT. MED.; RENNES)Thesis

"COMPLETE 5P" TRISOMY: 1 CASE AND 19 TRANSLOCATION CARRIERS IN 6 GENERATIONS.BRIMBLECOMBE FSW; LEWIS FJ; VOWLES M et al.1977; J. MED. GENET.; G.B.; DA. 1977; VOL. 14; NO 4; PP. 271-275; BIBL. 9 REF.Article

A NEW CASE OF PARTIAL TRISOMY 15Q-GENEIX A; JAFFRAY JY; MALET P et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 51; NO 3; PP. 335-338; BIBL. 10 REF.Article

THE 9P-DELETION SYNDROME. A PATIENT WITH A 45, XX, -9, -15, + T(9/15) CONSTITUTION DUE TO MATERNAL 3:1 MEIOTIC DISJUNCTION.BERGAMO F; CROSATO F; FRANCESCONI D et al.1977; CLIN. GENET.; DENM.; DA. 1977; VOL. 11; NO 3; PP. 219-223; BIBL. 10 REF.Article

TRISOMY FOR THE SHORT ARMS OF CHROMOSOME 9 IN TWO GENERATIONS, WITH BALANCED TRANSLOCATIONS T (15 P+; 9Q-) IN THREE GENERATIONS = TRISOMIE DES BRAS COURTS DU CHROMOSOME 9 DANS DEUX GENERATIONS, AVEC TRANSLOCATION BALANCEE T (15 P+; 9Q-) DANS TROIS GENERATIONSPODRUCH PE; WEISSKOPF B.1974; J. PEDIATR.; U.S.A.; DA. 1974; VOL. 85; NO 1; PP. 92-95; BIBL. 6 REF.Article

CYTOGENETICS OF 50 PATIENTS WITH MENTAL RETARDATION AND MULTIPLE CONGENITAL ANOMALIES AND 50 NORMAL SUBJECTS. MADISON BLIND STUDY IVMAGNELLI NC.1976; CLIN. GENET.; DENM.; DA. 1976; VOL. 9; NO 2; PP. 169-182; BIBL. 23 REF.Article

FAMILIAL TRANSLOCATION (3P 15P) WITH PARTIAL TRISOMY FOR THE UPPER ARM OF CHROMOSOME 3 IN TWO SIBS.SAY B; BARBER N; BOBROW M et al.1976; J. PEDIATR.; U.S.A.; DA. 1976; VOL. 88; NO 3; PP. 447-450; BIBL. 3 REF.Article

OSSERVAZIONE FAMILIARE DI DUE CASI DI TRISOMIA 4 P. = OBSERVATION FAMILIALE DE 2 CAS DE TRISOMIE 4PDEDE A; CAPIZZI M.1979; MINERVA PEDIATR.; ITA; DA. 1979; VOL. 31; NO 17; PP. 1281-1284; ABS. ENG; BIBL. 16 REF.Article

TRISOMIE 4P DE NOVO PAR ISOCHROMOSOME 4P.ANDRE MJ; AURIAS A; DE BERRANGER P et al.1976; ANN. GENET.; FR.; DA. 1976; VOL. 19; NO 2; PP. 127-131; ABS. ANGL.; BIBL. 16 REF.Article

IDENTIFICATION DE DEUX TRANSLOCATIONS FAMILIALESLAURENT C; BIEMONT MC; ROBERT JM et al.1974; SEM. HOP., ANN. GENET.; FR.; DA. 1974; VOL. 17; NO 4; PP. 279-281; ABS. ANGL.; BIBL. 8REF.Serial Issue

AN UNUSUAL CHROMOSOMAL SEGREGATION IN A FAMILY WITH A TRANSLOCATION BETWEEN CHROMOSOMES 3 AND 12 = SEGREGATION CHROMOSOMIQUE INHABITUELLE DANS UNE FAMILLE CONDUCTRICE D'UNE TRANSLOCATION ENTRE LES CHROMOSOMES 3 ET 12SACHDEVA S; SMITH GF; JUSTICE P et al.1974; J. MED. GENET.; G.B.; DA. 1974; VOL. 11; NO 3; PP. 303-305; BIBL. 4 REF.Article