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ARE 1Q+ CHROMOSOMES HARMLESS. = LES CHROMOSOMES 1Q+ SONT-ILS INOFFENSIFS.GARDNER RJM; MCCREANOR HR; PARSLOW MI et al.1974; CLIN. GENET.; DENM.; DA. 1974; VOL. 6; NO 5; PP. 383-393; BIBL. 1P.1/2Article

ETUDE CYTOGENETIQUE D'UN CAS DE SYNDROME DE FANCONI AVEC INVERSION PERICENTRIQUE FAMILIALE.CRIPPA L; FERRIER S.1975; J. GENET. HUM.; SUISSE; DA. 1975; VOL. 23; NO 1; PP. 7-16; ABS. ANGL. ALLEM.; BIBL. 13 REF.Article

A (1; 15) TRANSLOCATION, BALANCED, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO GM-126PRESCOTT GH; MCCAW BK; TOLBY BE et al.1975; CYTOGENET. CELL GENET.; SWITZ.; DA. 1975; VOL. 14; NO 1; PP. 84-85; BIBL. 1REF.Article

A (132) TRANSLOCATION, BALANCED, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO. GM-257ALFI OS; MILLER RC; GREENE AE et al.1975; CYTOGENET. CELL GENET.; SWITZ.; DA. 1975; VOL. 14; NO 2; PP. 154-155Article

GIEMSA BANDING OF CHROMOSOME 1 QH+ AND LINKAGE ANALYSIS = COLORATION EN BANDES PAR LE GIEMSA D'UN CHROMOSOME 1 QH+ ET ANALYSE DES LIAISONSHOWARD PN; STODDARD GR; GODDARD MW et al.1975; J. MED. GENET.; G.B.; DA. 1975; VOL. 12; NO 1; PP. 44-48; BIBL. 21 REF.Article

AN (X; 1) TRANSLOCATION, BALANCED, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO GM-97PUNNETT HH; KISTERMACHER ML; GREENE AE et al.1974; CYTOGENET. CELL GENET; SWITZ.; DA. 1974; VOL. 13; NO 4; PP. 406-407; BIBL. 1 REF.Article

A 1Q42 DELETION IN A VIETNAMESE INFANTNEU RL; AVILA DA; REDDINGTON JM et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 3; PP. 154-155; ABS. FRE; BIBL. 2 REF.Article

INTERSTITIAL DELETION 2Q31->Q33BUCHANAN PD; RHODES RL; STEVENSON CE JR et al.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 15; NO 1; PP. 121-126; BIBL. 2 P.Article

BREAK POINTS IN CHROMOSOME #1 ABNORMALITIES OF 218 HUMAN NEOPLASMSBRITO BABAPULLE V; ATKIN NB.1981; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1981; VOL. 4; NO 3; PP. 215-225; BIBL. 79 REF.Article

FAMILIAL PARACENTRIC INVERSION OF 1 PROMAIN DR; COLUMBANO GREEN LM; WHYTE S et al.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 14; NO 4; PP. 629-634; BIBL. 9 REF.Article

PARTIAL DISTAL 1 Q TRISOMY. A DISTINCT CLINICAL DYSMORPHIC SYNDROME IN ADULTHOODFRYNS JP; DE MUELENAERE A; PEDERSEN J et al.1980; ANN. GENET.; FRA; DA. 1980; VOL. 23; NO 3; PP. 181-182; ABS. FRE; BIBL. 7 REF.Article

PARTIAL TRISOMY 2Q SYNDROMEREHDER H; FRIEDRICH U.1979; CLIN. GENET.; DNK; DA. 1979; VOL. 15; NO 6; PP. 534-540; BIBL. 13 REF.Article

POSSIBLE TRISOMY 1Q25->1Q32 IN A MALFORMED GIRL WITH A DE NOVO INSERTION IN 1QSCHINZEL A.1979; HUM. GENET.; DEU; DA. 1979; VOL. 49; NO 2; PP. 167-173; BIBL. 4 REF.Article

CHROMOSOMES 1 IN 14 OVARIAN CANCERS. HETEROCHROMATIN VARIANTS AND STRUCTURAL CHANGES.ATKIN NB; PICKTHALL VJ.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 38; NO 1; PP. 25-33; BIBL. 14 REF.Article

PARTIAL TRISOMY OF THE LONG ARM OF CHROMOSOME 1 IN MYELOFIBROSIS AND POLYCYTHEMIA.HSU LYF; PINCHIAROLI D; GILBERT HS et al.1977; AMER. J. HEMATOL.; U.S.A.; DA. 1977; VOL. 2; NO 4; PP. 375-383; BIBL. 12 REF.Article

PERICENTRIC INVERSION OF CHROMOSOME 1. FREQUENCY AND POSSIBLE ASSOCIATION WITH CANCER.ATKIN NB; BAKER MC.1977; CYTOGENET. CELL GENET.; SWITZ.; DA. 1977; VOL. 19; NO 2-3; PP. 180-184; BIBL. 10 REF.Article

ANOMALIE DE FREQUENCE DU CHROMOSOME 1 QH+ DANS LA LEUCEMIE MYELOIDE CHRONIQUE.BERGER R; BERNHEIM A.1977; C.R. ACAD. SCI., D; FR.; DA. 1977; VOL. 285; NO 12; PP. 1183-1185; ABS. ANGL.; BIBL. 4 REF.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

PARTIAL INVERSION OF THE SECONDARY CONSTRICTION OF CHROMOSOME 9: IT EXISTSNERI G; TEDESCHI B; SANFILIPPO S et al.1982; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1982; VOL. 61; NO 1; PP. 80-81; BIBL. 7 REF.Article

INTERSTITIAL DELETION IN THE LONG ARM OF CHROMOSOME 1 IN A SUBJECT WITH CONGENITAL ABNORMALITIES. REPOSITORY IDENTIFICATION NO. GM-214DE LA CHAPELLE A; KOIVISTO M; ARONSON MM et al.1979; CYTOGENET. CELL GENET.; CHE; DA. 1979; VOL. 23; NO 3; PP. 220; BIBL. 1 REF.Article

PARTIAL TRISOMY 19 SYNDROMEREHDER H; FRIEDRICH U.1979; CLIN. GENET.; DNK; DA. 1979; VOL. 15; NO 6; PP. 534-540; BIBL. 13 REF.Article

TERMINAL LONG-ARM DELETION OF CHROMOSOME 1 IN A MALE INFANTDIGNAN PSJ; SOUKUP S.1979; HUM. GENET.; DEU; DA. 1979; VOL. 48; NO 2; PP. 151-156; BIBL. 10 REF.Article

A CASE OF PARTIAL (9Q) TRISOMY IN A FAMILY WITH A BALANCED TRANSLOCATION 46, XX, T(1P+9Q-).MASON MK; SPENCER DA; RUTTER A et al.1975; J. MED. GENET.; G.B.; DA. 1975; VOL. 12; NO 3; PP. 310-314; BIBL. 9 REF.Article

ETUDE CHEZ TROIS SUJETS STERILES DE TRANSLOCATIONS IMPLIQUANT LE CHROMOSOME 1TEYSSIER M; MOREAU N.1982; BULL. ASSOC. ANAT.; ISSN 0376-6160; FRA; DA. 1982; VOL. 66; NO 193; PP. 263-272; ABS. ENG; BIBL. 2 P.Article

CYTOGENETIC RECOGNITION OF CHROMOSOMAL DUPLICATION (DUP(1) (P31.4->P22.1)) AND THE DETECTION OF THREE DIFFERENT ALLELES AT THE PGM1 LOCUSCOUSINEAU AJ; HIGGINS JV; HACKEL E et al.1981; ANN. HUM. GENET.; ISSN 0003-4800; GBR; DA. 1981; VOL. 45; NO 4; PP. 337-340; BIBL. 7 REF.Article

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