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kw.\*:("ABNORMAL D13 CHROMOSOME")

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A CASE OF D13 RING CHROMOSOMECOSSU P; DIANA G; MAMELI M et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 46; NO 1; PP. 111-114; BIBL. 10 REF.Article

CHROMOSOME 13 EN ANNEAUHEVIA A; BULLON M; NOVALES A et al.1979; ANN. GENET.; FRA; DA. 1979; VOL. 22; NO 4; PP. 232-233; ABS. ENG; BIBL. 7 REF.Article

THE RING CHROMOSOME 13 SYNDROMEMARTIN NJ; HARVEY PJ; PEARN JH et al.1982; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1982; VOL. 61; NO 1; PP. 18-23; BIBL. 23 REF.Article

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

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

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

RETINOBLASTOMA AND ITS ASSOCIATION WITH A DELETION IN CHROMOSOME #13: A SURVEY USING HIGH-RESOLUTION CHROMOSOME TECHNIQUESJOHNSON MP; RAMSAY N; CERVENKA J et al.1982; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1982; VOL. 6; NO 1; PP. 29-37; BIBL. 34 REF.Article

TRISOMIE PARTIELLE DU SEGMENT DISTAL DU BRAS LONG DU CHROMOSOME 13 ET SON DIAGNOSTIC PRENATALZOLOTUKHINA TV; ROZOVSKIJ IS; BARTSEVA OB et al.1982; GENETIKA; ISSN 0016-6758; SUN; DA. 1982; VOL. 18; NO 11; PP. 1899-1905; ABS. ENG; BIBL. 13 REF.Article

MEIOTIC CONSEQUENCES OF PERICENTRIC INVERSIONS OF CHROMOSOME 13WENGER SL; STEELE MW.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 9; NO 4; PP. 275-283; BIBL. 34 REF.Article

PERICENTRIC INVERSION (13) WITH TWO DIFFERENT RECOMBINANTS IN THE SAME FAMILYWILLIAMSON EM; MILLER JF; SEABRIGHT M et al.1980; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1980; VOL. 17; NO 4; PP. 309-312; BIBL. 6 REF.Article

INTERSTITIAL DELETION OF 13Q ASSOCIATED WITH RETINOBLASTOMA AND CONGENITAL MALFORMATIONSPETIT P; FRYNS JP.1979; ANN. GENET.; FRA; DA. 1979; VOL. 22; NO 2; PP. 106-107; ABS. FRE; BIBL. 9 REF.Article

A 13; 13 TANDEM CHROMOSOME TRANSLOCATION IN A SUBJECT WITH CONGENITAL ANOMALIES: REPOSITORY IDENTIFICATION NO.GM 2018KOHN G; COHEN MM; ARONSON MM et al.1979; CYTOGENET. CELL GENET.; CHE; DA. 1979; VOL. 24; NO 1; PP. 72; BIBL. 1 REF.Article

PARTIAL TRISOMY 13 PRESUMABLY DUE TO RECOMBINATION IN AN INVERSION HETEROZYGOTE AND BY UNEQUAL CROSSING-OVER.KOSKE WESTPHAL T; PRUSZAK SEEL RE; NISS R et al.1978; ANN. HUM. GENET.; G.B.; DA. 1978; VOL. 41; NO 3; PP. 315-322; H.T. 2; BIBL. 22 REF.Article

RETINOBLASTOMA AND SUBBAND DELETION OF CHROMOSOME 13.YUNIS JJ; RAMSAY N.1978; AMER. J. DIS. CHILD.; U.S.A.; DA. 1978; VOL. 132; NO 2; PP. 161-163; BIBL. 17 REF.Article

TRISOMIE 13QTER PAR DUPLICATION EN TANDEM 46,XX, DIR DUP 13(Q21->QTER), 9QH+DE GROUCHY J; TURLEAU C; DANIS F et al.1978; ANN. GENET.; FRA; DA. 1978; VOL. 21; NO 4; PP. 247-251; ABS. ENG; BIBL. 37 REF.Article

DOES FULL MONOSOMY 21 EXIST. A COMMENT TO THE PAPER: A MALE INFANT WITH MONOSOMY 21 BY Y. KANEKO, T. IKEUCHI, M. SASAKI, Y. SATAKE AND S. KUWAJIMA.SCHINZEL A.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 32; NO 1; PP. 105-107; BIBL. 6 REF.Article

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