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Results 1 to 25 of 21129

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MONOZYGOTIC TWINS WITH RING CHROMOSOME 22 = JUMEAUX MONOZYGOTES PORTEURS D'UN CHROMOSOME 22 ANNULAIRELINDENBAUM RH; BOBROW M; BARBER L et al.1973; J. MED. GENET.; G.B.; DA. 1973; VOL. 10; NO 1; PP. 85-89; BIBL. 26 REF.Serial Issue

CHROMOSOMEY LONG (YQ+) ET ANOMALIES DU PHENOTYPE. ETUDE EN FLUORESCENCEGIRAUD F; MATTEI MG; HARTUNG M et al.1973; PEDIATRIE; FR.; DA. 1973; VOL. 28; NO 2; PP. 171-183; BIBL. 2P.Serial Issue

HETEROMORPHISME DES HOMOLOGUES DE LA PREMIERE PAIRE DE CHROMOSOMES CHEZ LE PERE, COMBINE A UN SYNDROME DE PATAU PHENOTYPIQUE CHEZ LE FOETUSKULAZHENKO VP; LAZYUK GI; MIKEL'SAAR AVN et al.1973; GENETIKA; S.S.S.R.; DA. 1973; VOL. 9; NO 3; PP. 138-148; H.T. 1; ABS. ANGL.; BIBL. 1P.1/2Serial Issue

ON THE ABSENCE OF CYTOPLASMIC DETERMINATION OF THE FORMATION OF MEGACHROMOSOMES IN NICOTIANAGERSTEL DU; BURNS JA.1972; J. HERED.; U.S.A.; DA. 1972; VOL. 63; NO 5; PP. 256-258; BIBL. 4REF.Serial Issue

RING F CHROMOSOME MOSAICISM (46,XY,20R/46,XY) IN AN EPILEPTIC CHILD WITHOUT APPARENT HAEMATOLOGICAL DISEASE = MOSAIQUE AVEC CHROMOSOME F ANNULAIRE (46,XY, 20R/46,XY) CHEZ UN ENFANT EPILEPTIQUE SANS MALADIE HEMATOLOGIQUE DEMONTREEFAED M; MORTON HG; ROBERTSON J et al.1972; J. MED. GENET.; G.B.; DA. 1972; VOL. 9; NO 4; PP. 470-473; BIBL. 14 REF.Serial Issue

ETUDE CYTOGENETIQUE DE LA VARIABILITE DES CHROMOSOMES ANNULAIRES CHEZ DROSOPHILA. I. LEURS EFFETS SUR LE SEXE ET LES DIFFERENTS STADES DU DEVELOPPEMENTSTEPANOVA NL.1972; GENETIKA; S.S.S.R.; DA. 1972; VOL. 8; NO 8; PP. 90-97; ABS. ANGL.; BIBL. 1P.1/2Serial Issue

IL CROMOSOMA 18 AD ANELLO. OSSERVAZIONE CLINICA E CONSIDERAZIONI CARIOLOGICHE = LE CHROMOSOME 18 EN ANNEAU. OBSERVATION CLINIQUE ET ETUDE DU CARYOTYPEGIOVANNUCCI UZIELLI ML; CARBONE C; CALABRI G et al.1972; MINERVA PEDIATR.; ITAL.; DA. 1972; VOL. 24; NO 36; PP. 1707-1714; ABS. ANGL.; BIBL. 31 REF.Serial Issue

A FERTILE MALE RABBIT WITH A MINUTE Y CHROMOSOME = UN LAPIN MALE FERTILE PORTEUR D'UN PETIT CHROMOSOME YMARTIN PA; SHAVER EL.1972; J. EXPER. ZOOL.; U.S.A.; DA. 1972; VOL. 81; NO 1; PP. 87-97; BIBL. 22 REF.Serial Issue

D1 RING CHROMOSOME IN NEWBORN WITH PECULIAR FACE, POLYDACTYLY, IMPERFORATE ANUS, ARRHINENCEPHALY, AND OTHER MALFORMATIONS = CHROMOSOME D1 EN ANNEAU CHEZ UN NOUVEAU-NE AVEC FACIES PARTICULIER, POLYDACTYLIE, IMPERFORATION ANALE, ARRHINENCEPHALIE ET D'AUTRES MALFORMATIONSBILES AR JR; LUEERS T; SPERLING K et al.1970; J. MED. GENET.; G.B.; DA. 1970; VOL. 7; NO 4; PP. 399-401; BIBL. 17 REF.Serial Issue

CHROMOSOMAL ANALYSIS OF METASTATIC RETINOBLASTOMA CELLS = ANALYSE CHROMOSOMIQUE DES CELLULES DE RETINOBLASTOME METASTATIQUEINOUE S; YADDANAPUDI RAVINDRANATH; OTTENBREIT MJ et al.1974; HUMANGENETIK; DTSCH.; DA. 1974; VOL. 25; NO 2; PP. 111-118; BIBL. 16REF.Article

MARKER CHROMOSOMES IN PARENTS OF SPONTANEOUS ABORTUSES = LES CHROMOSOMES MARQUEURS CHEZ LES PARENTS DE PRODUITS D'AVORTEMENTS SPONTANESHOLBEK S; FRIEDRICH U; LAURITSEN JG et al.1974; HUMANGENETIK; DTSCH.; DA. 1974; VOL. 25; NO 1; PP. 61-64; BIBL. 17REF.Article

CHROMOSOME NUMBER18CURTIS DJ.1973; HUMANGENETIK; DTSCH.; DA. 1973; VOL. 18; NO 3; PP. 273-277; ABS. ALLEM.; BIBL. 6REF.Serial Issue

RING CHROMOSOME 7 WITH VARIABLE PHENOTYPIC EXPRESSION1973; CYTOGENET. CELL GENET.; SWITZ.; DA. 1973; VOL. 12; NO 1; PP. 40-48; BIBL. 1P.Serial Issue

THE INFLUENCE OF INACTIVE CHROMOSOMES ON HUMAN DEVELOPMENT. ANOMALOUS SEX CHROMOSOME COMPLEMENTS AND THE PHENOTYPE = L'INFLUENCE DES CHROMOSOMES INACTIFS SUR LE DEVELOPPEMENT HUMAIN. COMPLEMENTS CHROMOSOMIQUES SEXUELS ANORMAUX ET PHENOTYPEBARLOW P.1973; HUMANGENETIK; DTSCH.; DA. 1973; VOL. 17; NO 2; PP. 105-136; ABS. ALLEM.; BIBL. 8P.1/2Serial Issue

TRANSMISSION HEREDITAIRE, DEPUIS 300ANS, D'UN CHROMOSOMEY A SATELLITES DANS UNE LIGNEE FAMILIALEGENEST P.1973; SEM. HOP., ANN. GENET.; FR.; DA. 1973; VOL. 16; NO 1; PP. 35-38; ABS. ANGL.; BIBL. 4REF.Serial Issue

IDENTIFICATION BY FLUORESCENCE OF TWO G RINGS: (46XY, 21R) G DELETION SYNDROME I AND (46, XX, 22R) G DELETION SYNDROME IIMAGENIS RE; ARMENDARES S; HECHT F et al.1972; SEM. HOP., ANN. GENET.; FR.; DA. 1972; VOL. 15; NO 4; PP. 265-266; ABS. FR.Serial Issue

TRISOMY-18 SYNDROME CAUSED BY TRANSLOCATION OR ISOCHROMOSOME FORMATION. A CASE REPORT WITH BIBLIOGRAPHY = SYNDROME DE TRISOMIE 18 PAR TRANSLOCATION OU FORMATION D'ISOCHROMOSOMES. OBSERVATION D'UN CAS ET BIBLIOGRAPHIEMUELLER H; BUEHLER EM; SIGNER E et al.1972; J. MED. GENET.; G.B.; DA. 1972; VOL. 9; NO 4; PP. 462-467; BIBL. 14 REF.Serial Issue

CHROMOSOME 15 EN ANNEAU: R (15). IDENTIFICATION PAR DENATURATION MENAGEEFORABOSCO A; DUTRILLAUX B; VAZZOLER G et al.1972; SEM. HOP., ANN. GENET.; FR.; DA. 1972; VOL. 15; NO 4; PP. 267-270; ABS. ANGL.; BIBL. 14REF.Serial Issue

AN ABNORMAL LARGE HUMAN CHROMOSOME IDENTIFIED AS AN END-TO-END FUSION OF TWO X'S BY COMBINED RESULTS OF THE NEW BANDING TECHNIQUES AND MICRODENSITOMETRY = UN CHROMOSOME HUMAIN ANORMAL DE GRANDE TAILLE IDENTIFIE COMME LA FUSION TERMINO-TERMINALE DE DEUX X PAR LES RESULTATS COMBINES DES NOUVELLES TECHNIQUES DE COLORATION DES BANDES ET DE LA MICRODENSIMETRIEDISTECHE C; HAGEMEIJER A; FREDERIC J et al.1972; CLIN. GENT.; DANM.; DA. 1972; VOL. 3; NO 5; PP. 388-395; BIBL. 17 REF.Serial Issue

LE LIQUIDE AMNIOTIQUE ET LES POSSIBILITES DIAGNOSTIQUES OFFERTES PAR L'AMNIOCENTESE.DE GRANDI P.1975; REV. MED. SUISSE ROMANDE; SUISSE; DA. 1975; VOL. 95; NO 6; PP. 445-478Article

FREQUENCY OF SATELLITE ASSOCIATION IN INDIVIDUALS WITH STRUCTURAL ABNORMALITIES OF NUCLEOLUS ORGANISER REGION = FREQUENCE DES ASSOCIATIONS DE SATELLITES CHEZ LES INDIVIDUS PRESENTANT DES ANOMALIES DE STRUCTURE DE LA REGION DE L'ORGANISATEUR NUCLEOLAIREDE CAPOA A; ROCCHI A; GIGLIANI F et al.1973; HUMANGENETIK; DTSCH.; DA. 1973; VOL. 18; NO 2; PP. 111-115; ABS. ALLEM.; BIBL. 17REF.Serial Issue

INHERITED CONSTRICTION FRAGILITY OF CHROMOSOME 2FERGUSON SMITH MA.1973; SEM. HOP., ANN. GENET.; FR.; DA. 1973; VOL. 16; NO 1; PP. 29-34; ABS. FR.; BIBL. 19REF.Serial Issue

KARYOTYPE EVOLUTION IN HUMAN LEUKAEMIA. THE RELATION BETWEEN KARYOTYPES, CELLULAR PHENOTYPES AND CLINICAL PROGRESSION = L'EVOLUTION CARYOTYPIQUE DANS LES LEUCEMIES HUMAINES. RAPPORT ENTRE CARYOTYPES, PHENOTYPES CELLULAIRES ET EVOLUTION CLINIQUEPEDERSON B.1973; EXCERPTA MED., INTERNATION. CONGR. SER.; PAYS-BAS; DA. 1973; PP. 167-176; BIBL. 1P.1/2; (C.R. IVE CONGR. INT. GENET. HUM.; PARIS; 1971)Conference Paper

TWO KINSHIPS WITH ACCESSORY BISATELLITED CHROMOSOMESSOUDEK D; MCCREARY BD; LARAYA P et al.1973; SEM. HOP., ANN. GENET.; FR.; DA. 1973; VOL. 16; NO 2; PP. 101-107; ABS. FR.; BIBL. 29REF.Serial Issue

A HUMAN FAMILY SUGGESTING EVIDENCE FOR CENTRIC FISSION AND STABILITY OF A TELOCENTRIC CHROMOSOME = UNE FAMILLE HUMAINE IMPLIQUANT UNE POSSIBILITE DE DIVISION CENTRIQUE ET DE STABILITE D'UN CHROMOSOME TELOCENTRIQUESINHA AK; SEN PATHAK; NORA JJ et al.1972; HUM. HERED.; SWITZ.; DA. 1972; VOL. 22; NO 5-6; PP. 423-429; BIBL. 8REF.Serial Issue

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