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Results 1 to 25 of 501132

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ANOMALIES DE STRUCTURE DU CHROMOSOME X ISOCHROMOSOMES ET DELETIONSPHALIPPON JL.1975; LYON; ASSOC. CORP. ETUD. MED.; DA. 1975; PP. 1-78; BIBL. 9P.; (THESE DOCT. MED.; CLAUDE BERNARD LYON)Thesis

STRUCTURAL ABERRATIONS OF THE X CHROMOSOME IN MAN.DAVIDENKOVA EF; VERLINSKAJA DK; MASHKOVA MV et al.1978; HUM. GENET.; GERM.; DA. 1978; VOL. 41; NO 3; PP. 269-279; BIBL. 19 REF.Article

OVARIAN DIFFERENTIATION IN TURNER'S SYNDROME.RIVELIS CF; COCO R; BERGADA C et al.1978; J. GENET. HUM.; SUISSE; DA. 1978; VOL. 26; NO 1; PP. 69-83; ABS. FR. ALLEM.; BIBL. 15 REF.Article

REAPPRAISAL OF A 46, X, I(XP) KARYOTYPE AS 46, X, DEL(XQ).DE LA CHAPELLE A; SCHRODER J.1975; HEREDITAS; SUEDE; DA. 1975; VOL. 80; NO 1; PP. 137-140; BIBL. 11 REF.Article

RECOMBINANT CHROMOSOME AS A RESULT OF PERICENTRIC INVERSION OF X CHROMOSOMENIKOLIS J; STOLEVIC E.1978; HUM. GENET.; DEU; DA. 1978; VOL. 45; NO 2; PP. 115-122; BIBL. 13 REF.Article

INCREASED Q FLUORESCENCE OF AN INACTIVE XQ-CHROMOSOME IN MAN = FLUORESCENCE Q PLUS INTENSE D'UN CHROMOSOME HUMAIN XQ-INACTIFSARTO GE; THERMAN E; PATAU K et al.1974; CLIN. GENET.; DENM.; DA. 1974; VOL. 6; NO 4; PP. 289-293; BIBL. 12REF.Article

A DUPLICATION-DEFICIENCY X CHROMOSOME IN A GIRL WITH SEVERE MENTAL RETARDATIONSACCHI N; DALPRA L; KEHYAYAN E et al.1980; HUM. GENET.; DEU; DA. 1980; VOL. 54; NO 2; PP. 279-281; BIBL. 10 REF.Article

ETUDE CYTOGENETIQUE DE LA MALADIE DU CRI DU CHAT. A PROPOS D'UNE FAMILLE OU TROIS ENFANTS SONT ATTEINTS DE L'AFFECTION ET UN DE SA RECIPROQUEBOUVIER G.1974; LYON; ASSOC. CORP. ETUD. MED. LYON; DA. 1974; PP. 1-62; BIBL. 19P.; (THESE DOCT. MED.; CLAUDE-BERNARD LYON)Thesis

CYTOLOGICAL FINDINGS OF 10 CASES WITH I(XQ) AND ONE WITH DIC(X) (QTER->CEN->P22::P11->QTER).FUJITA H; TANIGAWA Y; YOSHIDA Y et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 39; NO 2; PP. 147-155; BIBL. 18 REF.Article

A22/22 TRANSLOCATION CARRIER WITH RECURRENT ABORTIONS DEMONSTRATED BY A GIEMSA BANDING TECHNIQUEMAEDA T; OHNO M; SHIMADA N et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 31; NO 2; PP. 243-245; BIBL. 11 REF.Article

CHROMOSOME X AVEC DELETION D'UN BRAS LONG.GILGENKRANTZ S; BAUE G.1977; J. GYNECOL. OBSTETR. BIOL. REPROD.; FR.; DA. 1977; VOL. 6; NO 3; PP. 337-345; ABS. ANGL.; BIBL. 1 P.Article

ANALYSIS OF DNA REPLICATION PATTERNS OF HUMAN FIBROBLAST CHROMOSOMES. THE REPLICATION MAP.KONDRA PM; RAY M.1978; HUM. GENET.; DEU; DA. 1978; VOL. 43; NO 2; PP. 139-149; BIBL. 2 P.Article

RELATION ENTRE ISOCHROMOSOME XQ ET DEFICIT SERIQUE EN IMMUNOGLOBULINE ACHOUDAT D; TAILLEMITE JL; HIRSCH MARIE H et al.1979; NOUV. PRESSE MED.; FRA; DA. 1979; VOL. 8; NO 29; PP. 2419; BIBL. 4 REF.Article

A TEEN-AGER WITH 46, X, DEL (X) (Q 21)SRIVASTAVA PK; FRISTOE F JR; MCDAVID RE et al.1979; SOUTH. MED. J.; USA; DA. 1979; VOL. 72; NO 11; PP. 1461-1463; BIBL. 10 REF.Article

PARTIAL LONG ARM DELETION OF ONE X CHROMOSOME IN A PATIENT WITH SECONDARY AMENORRHEARUTHNER U; MASCHIK S; BREITENECKER G et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 48; NO 1; PP. 135-137; BIBL. 3 REF.Article

CYTOGENETIC STUDIES IN SEVEN INDIVIDUALS WITH AN I(XQ) KARYTOYPE.NIEBUHR E; SKOVBY F.1977; HEREDITAS; SUEDE; DA. 1977; VOL. 86; NO 1; PP. 121-128; BIBL. 43 REF.Article

DICENTRIC X-ISOCHROMOSOME (XQI DIC) AND PERICENTRIC INVERSION OF NO.2 (INV(2)(P15Q21)) IN A PATIENT WITH GONADAL DYSGENESIS = ISOCHROMOSOME X DICENTRIQUE (XQI DIC) ET INVERSION PERICENTRIQUE DU NO 2 (INV(2)(P15Q21)) CHEZ UN MALADE ATTEINT DE DYSGENESIE GONADIQUECOHEN MM; ROSENMANN A; HACHAM ZADEH S et al.1975; CLIN. GENET.; DENM.; DA. 1975; VOL. 8; NO 1; PP. 11-17; BIBL. 16 REF.Article

IDENTIFICATION OF PH1 CHROMOSOME AND ASSOCIATED TRANSLOCATION IN CHRONIC MYELOGENOUS LEUKEMIA BY HOECHST 33258 = IDENTIFICATION DU CHROMOSOME PH1 ET DE LA TRANSLOCATION ASSOCIEE DANS LA LEUCEMIE MYELOIDE CHRONIQUE PAR LE HOECHST 33258RAPOSA T; NATARAJAN AT; GRANBERG I et al.1974; J. NATION. CANCER INST.; U.S.A.; DA. 1974; VOL. 52; NO 6; PP. 1935-1938; BIBL. 15REF.Article

A BOY WITH 47,X, DEL(X) (P11->Q13: :Q21->Q24), DEL(Y) (Q11). REEXAMINATION OF A CASE PREVIOUSLY DESCRIBED AS 47,XY,.YQNIELSEN J; RASMUSSEN K; SILLESEN I et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 31; NO 2; PP. 227-230; BIBL. 10 REF.Article

PARTIAL TRISOMY 4Q AND PARTIAL MONOSOMY 18Q AS CONSEQUENCE OF A PATERNAL BALANCED TRANSLOCATION T(4Q; 18Q+)FONATSCH C; FLATZ SD; HURTER P et al.1974; HUMANGENETIK; DTSCH.; DA. 1974; VOL. 25; NO 3; PP. 227-233; BIBL. 8REF.Article

PRIMARY AMENORRHEA WITH A NEW MOSAIC 46, XXQI/47, XXQI XP-. CONSIDERATION ON THE X ISOCHROMOSOME FORMATION AND X CHROMOSOME INACTIVATION.HALBRECHT I; SHABTAI F; KUPFERSTAIN C et al.1977; ACTA GENET. MED. GEMELLOL.; ITAL.; DA. 1977; VOL. 26; NO 1; PP. 63-69; ABS. ITAL. FR. ALLEM.; BIBL. 20 REF.Article

INHERITED PARTIAL DUPLICATION OF CHROMOSOME NO 15 = DUPLICATION PARTIELLE HEREDITAIRE DU CHROMOSOME NO 15FUJIMOTO A; TOWNER JW; EBBIN AJ et al.1974; J. MED. GENET.; G.B.; DA. 1974; VOL. 11; NO 3; PP. 287-291; BIBL. 9 REF.Article

POSITION OF THE HUMAN X INACTIVATION CENTER ON X9THERMAN E; SARTO GE; PALMER CG et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 50; NO 1; PP. 59-64; BIBL. 10 REF.Article

SYNDROMES DE TURNERQUEFFELEC JEAN PAUL.sd; FRA; DA. S.D.; 29411; 153-XXP.: ILL.; 30 CM; BIBL. 20 P.; TH.: MED./BREST/1979Thesis

CHROMOSOMAL AND CLINICAL FINDINGS IN 110 FEMALES WITH TURNER SYNDROME.PALMER CG; REICHMANN A.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 35; NO 1; PP. 35-49; BIBL. 1 P.Article

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