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HUMAN ACROCENTRIC RING CHROMOSOMES AND SATELLITE ASSOCIATION.CANTU JM; SALAMANCA F; SANCHEZ J et al.1975; ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 3; PP. 193-196; ABS. FR.; BIBL. 23 REF.Article

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Interstitial deletion of long arm of chromosome 13CARNEVALE, A; FRIAS, S; ALCANTAR, R et al.Annales de génétique (Paris). 1984, Vol 27, Num 1, pp 49-52, issn 0003-3995Article

DELINEATION OF 13Q, DELETION BY REPLICATION BANDING IN RETINOBLASTOMACAMARGO M; JOHNSON MP; CERVENKA J et al.1981; CYTOGENET. CELL GENET.; ISSN 0301-0171; CHE; DA. 1981; VOL. 31; NO 2; PP. 77-83; BIBL. 2 P.Article

OCULAR ABNORMALITY ASSOCIATED WITH PARTIAL DUPLICATION OF CHROMOSOME 13GINSBERG J; DIGNAN PSJ; BUCHINO JJ et al.1981; ANN. OPHTHALMOL.; ISSN 0003-4886; USA; DA. 1981; VOL. 13; NO 2; PP. 189-194; BIBL. 39 REF.Article

IRREGULAR PHENOTYPIC EXPRESSION OF RING CHROMOSOMES = EXPRESSION PHENOTYPIQUE IRREGULIERE DES CHROMOSOMES ANNULAIRESZDANSKY R; ANDRLE M; BUEHLER E et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 26; NO 3; PP. 193-198; ABS. ALLEM.; BIBL. 14REF.Article

RECURRENT ABORTIONS AND PATERNAL BALANCED TRANSLOCATION T (1Q-; 13Q+). = AVORTEMENTS RECURRENTS ET TRANSLOCATION BALANCEE T(1Q-; 13Q+) CHEZ LE PEREROZYNKOWA D; TREBICKA KWIATKOWSKA B; STEPIEN J et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 28; NO 4; PP. 349-351; BIBL. 7 REF.Article

RETINOBLOSTOMA AND CHROMOSOME ABNORMALITY. PARTIAL DELETION OF THE LONG ARM OF CHROMOSOME 13 = RETINOBLASTOME ET ANOMALIE CHROMOSOMIQUE. DELETION PARTIELLE DU BRAS LONG DU CHROMOSOME 13HOWARD RO; BREG WR; ALBERT DM et al.1975; ARCH. OPHTHALMOL.; U.S.A.; DA. 1975; VOL. 92; NO 6; PP. 490-493; BIBL. 21 REF.Article

DE NOVO DUPLICATION 13Q(46,XX,DUP(13) (Q21->Q333))FRACCARO M.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 58; NO 4; PP. 444Article

RING CHROMOSOME 13 IN A CHILD WITH MINOR DYSMORPHIC FEATURES, IRREGULAR PHENOTYPIC EXPRESSION OF RING 13 SYNDROMEVERMA RS; DOSIK H; CHOWDHRY IH et al.1978; AMER. J. DIS. CHILD; USA; DA. 1978; VOL. 132; NO 10; PP. 1018-1021; BIBL. 21 REF.Article

SEGREGATION OF AN INSERTIONAL CHROMOSOME REARRANGEMENT IN 3 GENERATIONSTOOMEY KE; MOHANDAS T; SPARKES RS et al.1978; J. MED. GENET.; GBR; DA. 1978; VOL. 15; NO 5; PP. 382-387; BIBL. 15 REF.Article

DELETION LONG ARM 13.NIELSEN J; HOMMA A; CHRISTIANSEN F et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 37; NO 3; PP. 339-345; BIBL. 12 REF.Article

TRANSMISSION OF A T(13Q22Q) CHROMOSOME ABSERVED IN THREE GENERATIONS WITH SEGREGATION OF THE TRANSLOCATION D1-TRISOMY SYNDROMEABE T; MORITA M; KAWAI K et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 30; NO 3; PP. 207-215; BIBL. 21 REF.Article

TRISOMY 13 WITH A 139149 TRANSLOCATION.COCO R; PENCHASZADEH B.1975; J. GENET. HUM.; SUISSE; DA. 1975; VOL. 23; NO 1; PP. 1-6; ABS. FR. ALLEM.; BIBL. 10 REF.Article

THE AETIOLOGY OF THE CAT EYE SYNDROME RECONSIDEREDGUANTI G.1981; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1981; VOL. 18; NO 2; PP. 108-118; BIBL. 23 REF.Article

DE NOVO 13Q PARACENTRIC INVERSION IN A BOY WITH CLEFT POLATE AND MENTAL RETARDATIONRICCARDI VM; HOLMQUIST GP.1979; HUM. GENET.; DEU; DA. 1979; VOL. 52; NO 2; PP. 211-215; BIBL. 12 REF.Article

INTERSTITIAL DELETION OF CHROMOSOME 13 AND ASSOCIATED CONGENITAL ANOMALIESNICHOLS WW; MILLER RC; HOFFMAN E et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 52; NO 2; PP. 169-173; BIBL. 1 P.Article

PARENTAL ORIGIN OF A RING 13 CHROMOSOME IN A FEMALE WITH MULTIPLE ANOMALIES.MAGENIS RE; WYANDT HE; OVERTON KM et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 33; NO 2; PP. 181-186; BIBL. 9 REF.Article

PARTIAL DELETIONS AND TRISOMIES OF CHROMOSOME 13; MAPPING OF BANDS ASSOCIATED WITH PARTICULAR MALFORMATIONS.NOEL B; QUACK B; RETHORE MO et al.1976; CLIN. GENET.; DENM.; DA. 1976; VOL. 9; NO 6; PP. 593-602; BIBL. 22 REF.Article

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