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Results 1 to 25 of 536

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LONG SURVIVAL IN TRISOMY-13-SYNDROME: 21 CASES INCLUDING PROLONGED SURVIVAL IN TWO PATIENTS 11 AND 19 YERS OLDREDHEENDRAN R; NEU RL; BANNERMAN RM et al.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 8; NO 2; PP. 167-172; BIBL. 7 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

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

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

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

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

RATES OF 47, +13 AND 46 TRANSLOCATION D/13 PATAU SYNDROME IN LIVE BIRTHS AND COMPARISON WITH RATES IN FETAL DEATHS AND AT AMNIOCENTESISHOOK EB.1980; AM. J. HUM. GENET.; ISSN 0002-9297; USA; DA. 1980; VOL. 32; NO 6; PP. 849-858; BIBL. 33 REF.Article

DEPISTAGE ECHOGRAPHIQUE DES ANOMALIES CHROMOSOMIQUES: A PROPOS DES TRISOMIES 13 ET 18AUBRY JP; AUBRY MC; HENRION R et al.1982; JOURNAL DE GENETIQUE HUMAINE; ISSN 0021-7743; CHE; DA. 1982; VOL. 30; NO 3; PP. 233-253; ABS. ENG; BIBL. 5 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

A DELETED CHROMOSOME NO. 13 IN HUMAN RETINOBLASTOMA CELLS: RELEVANCE TO TUMORIGENESISBALABAN MALENBAUM G; GILBERT F; NICHOLS WW et al.1981; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1981; VOL. 3; NO 3; PP. 243-250; BIBL. 24 REF.Article

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

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

Clinical delineation of proximal and distal partial 13q trisomyROGERS, J. F.Clinical genetics. 1984, Vol 25, Num 3, pp 221-229, issn 0009-9163Article

GENETIC MAPPING: CHROMOSOMES 6-22KEATS B.1982; AM. J. HUM. GENET.; ISSN 0002-9297; USA; DA. 1982; VOL. 34; NO 5; PP. 730-742; BIBL. 39 REF.Article

LYMPHOCYTE CHROMOSOME SURVEY IN 42 PATIENTS WITH RETINOBLASTOMA: EFFORT TO DETECT 13Q14 DELETION MOSAICISMMOTEGI T.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 58; NO 2; PP. 168-173; BIBL. 30 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

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