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Results 1 to 25 of 39265

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GROSS CONGENITAL ABNORMALITY ASSOCIATED WITH AN APPARENTLY BALANCED CHROMOSOMAL TRANSLOCATION T(9; 17) (Q34; Q11)DOCKERY HE; NEALE HC; FITZGERALD PH et al.1982; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1982; VOL. 19; NO 5; PP. 380-383; BIBL. 5 REF.Article

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

RESOLUTION OF BREAK POINTS IN A COMPLEX REARRANGEMENT BY USE OF MULTIPLE STAINING TECHNIQUES: CONFIRMATION OF SUSPECTED 12P12.3 INTRABAND BY DELETION DOSAGE EFFECT OF LDHBMAGENIS E; BROWN MG; CHAMBERLIN J et al.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 9; NO 2; PP. 95-103; BIBL. 12 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

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

15; 17 TRANSLOCATION IN ACUTE PROMYELOCYTIC LEUKEMIAFERRO MT; SAN ROMAN C; FERNANDEZ RANADA JM et al.1982; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1982; VOL. 7; NO 1; PP. 89-92; BIBL. 3 REF.Article

FAMILIAL TRANSLOCATION T(1;17)STEINBACH P.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 58; NO 4; PP. 444Article

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

PARTICULAR SECONDARY CHROMOSOME CHANGES IN CHRONIC LEUKEMIA T(8;17): REPORT OF TWO CASESPETIT P; VAN DEN BERGHE H.1981; ANN. GENET.; FRA; DA. 1981; VOL. 24; NO 1; PP. 25-27; ABS. FRE; BIBL. 7 REF.Article

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

STUDIO CITOGENITICO SU TUMORI GASTROINTESTINALI = ETUDE CYTOGENETIQUE DE TUMEURS GASTROINTESTINALESGRIMOLDI MG; LAVEZZI AM; UGAZIO P et al.1979; FOLIA HERED. PATHOL.; ITA; DA. 1979; VOL. 28; NO 2; PP. 27-31; ABS. ENG; BIBL. 5 REF.Article

A CASE OF PARTIAL TRISOMY 17 RESULTING FROM X-AUTOSOMAL TRANSLOCATIONYAMAMOTO Y; ENDO Y; KUROKI Y et al.1979; J. MED. GENET.; GBR; DA. 1979; VOL. 16; NO 5; PP. 395-399; BIBL. 6 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

A 15/17 TRANSLOCATION IN A PATIENT WITH PRADER-LABHART-WILLI SYNDROMECAVALLI IJ; SBALQUEIRO IJ; WAJNTAL A et al.1982; HUM. HERED.; ISSN 0001-5652; CHE; DA. 1982; VOL. 32; NO 3; PP. 149-151; BIBL. 17 REF.Article

CONSTITUTIONAL T(15;17)FERRO MT; SAN ROMAN C.1981; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1981; VOL. 4; NO 1; PP. 89-91; BIBL. 4 REF.Article

ASSOCIATION MALE XX, SYNDROME DE PIERRE ROBIN, TRANSLOCATION EQUILIBREE PATERNELLE 46XY,T(16;17) (P13;Q21)PETRUS M; BOURROUILLOU G; DUTAU G et al.1981; J. GENET. HUM.; ISSN 0021-7743; CHE; DA. 1981; VOL. 29; NO 2; PP. 191-196; ABS. ENG; BIBL. 21 REF.Article

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

CHROMOSOME ABNORMALITIES IN ACUTE PROMYELOCYTIC LEUKEMIA (APL)VAN DEN BERGHE H; LOUWAGIE A; BROECKAERT VAN ORSHOVEN A et al.1979; CANCER; USA; DA. 1979; VOL. 43; NO 2; PP. 558-562; BIBL. 4 REF.Article

CHROMOSOME ANALYSIS IN TWO UNUSUAL MALIGNANT BLOOD DISORDERS PRESUMABLY INDUCED BY BENZENEVAN DER BERGHE H; LOUWAGIE A; BROECKAERT VAN ORSHOVEN A et al.1979; BLOOD; USA; DA. 1979; VOL. 53; NO 4; PP. 558-566; BIBL. 18 REF.Article

TRISOMY 9 P WITH I(9P) AND T(9Q18P)HERVA R; KOIVISTO M.1979; HUM. GENET.; DEU; DA. 1979; VOL. 50; NO 3; PP. 237-240; BIBL. 7 REF.Article

A (3;17) BALANCED TRANSLOCATION, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO. GM-2808STENGEL RUTKOWSKI S; WIRTZ A; MURKEN JP et al.1979; CYTOGENET. CELL. GENET; CHE; DA. 1979; VOL. 24; NO 4; PP. 252Article

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