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kw.\*:("DELETION X BRAS COURT")

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TURNER'S SYNDROME WITH INTERSTITIAL AND PRESUMPTIVE TERMINAL DELETION SHORT ARM X.SILLESEN I; RASMUSSEN K; NIELSEN J et al.1976; AEREDITAS; SUEDE; DA. 1976; VOL. 84; NO 1; PP. 123-125; BIBL. 28 REF.Article

DELETION PARTIELLE DU BRAS COURT D'UN CHROMOSOME XGIRAUD F; HARTUNG M; MATTEI JF et al.1974; ARCH. FR. PEDIATR.; FR.; DA. 1974; VOL. 31; NO 7; PP. 717-724; ABS. ANGL.; BIBL. 1 P. 1/2Article

INHERITED INTERSTITIAL DEL (XP) WITH MINIMAL CLINICAL CONSEQUENCES: WITH A NOTE ON THE LOCATION OF GENES CONTROLLING PHENOTYPIC FEATURESHERVA R; KALUZEWSKI B; DE LA CHAPELLE A et al.1979; AMER. J. MED. GENET.; USA; DA. 1979; VOL. 3; NO 1; PP. 43-58; BIBL. 40 REF.Article

KARYOTYP-PHENOTYP-KORRELATION BEI EINEM 46, XDEL (X) (P22)-BEFUND = CORRELATION PHENOTYPE CARYOTYPE DANS UN DIAGNOSTIC 46, XDEL (X) (P22)BARTSCH SANDHOFF M; TERINDE R; WIEGELMANN W et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 31; NO 3; PP. 263-270; ABS. ANGL.; BIBL. 10 REF.Article

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

SHORT-ARM DELETION OF AN X CHROMOSOME (45,XO/46,XXP-).KAISER P; GERHARD RATSCHOW K; ZABEL B et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 37; NO 1; PP. 93-96; BIBL. 13 REF.Article

CHRISTMAS DISEASE (HAEMOPHILIA B) IN A GIRL WITH DELETION OF THE SHORT ARM OF ONE X-CHROMOSOME (FUNCTIONAL TURNER SYNDROME).SPINELLI A; SCHMID W; STRAUB PW et al.1976; BRIT. J. HAEMATOL.; G.B.; DA. 1976; VOL. 34; NO 1; PP. 129-135; BIBL. 19 REF.Article

UN CAS DE SYNDROME DE TURNER EN MOSAIQUE 45,X/46,XXP- ASSOCIE A UN DALTONISMEFERRIER S; CRIPPA L; CABROL C et al.1976; J. GENET. HUM.; SUISSE; DA. 1976; VOL. 24; NO 2; PP. 95-112; ABS. ANGL. ALLEM.; BIBL. 2 P. 1/2Article

PARTIAL SHORT ARM DELETION OF THE X CHROMOSOME 46, X, DEL(X) (QTER->P21:)KAOSAAR M; MIKELSAAR AV.1980; HUM. GENET.; DEU; DA. 1980; VOL. 53; NO 2; PP. 275-277; BIBL. 9 REF.Article

A NOTE ON THE XP-HOO JJ.1979; HUM. GENET.; DEU; DA. 1979; VOL. 50; NO 3; PP. 339-340; BIBL. 8 REF.Article

DOWN AND TURNER SYNDROMES IN A FEMALE INFANT WITH 47, X, DEL(X) (P11), +21.MARTSOLF JT; RAY M; BAUDER F et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 39; NO 1; PP. 103-108; BIBL. 15 REF.Article

DYSGENESIE OVARIENNE PAR TRANSLOCATION FAMILIALE, X SUR AUTOSOME. ALTERNANCE DE L'INACTIVATION DU CHROMOSOME X.FRANTZ J; NOEL B.1975; REV. FR. ENDOCRINOL. CLIN.; FR.; DA. 1975; VOL. 16; NO 5; PP. 445-453; ABS. ANGL.; BIBL. 6 REF.Article

A (4; 11) TRANSLOCATION, BALANCED, XXXXP-Y , 49CHROMOSOMES. REPOSITORY IDENTIFICATION NOGM-157DE LA CHAPELLE A; MILLER RC; GREENE AE et al.1975; CYTOGENET. CELL GENET.; SWITZ.; DA. 1975; VOL. 14; NO 1; PP. 76-77; BIBL. 3REF.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

CLINICAL CONSEQUENCE OF XP-HOO JJ.1979; HUM. GENET.; DEU; DA. 1979; VOL. 46; NO 3; PP. 349-351; BIBL. 9 REF.Article

X SHORT ARM DELETION IN A FEMALE SUBJECT WITH SPONTANEOUS SEXUAL DEVELOPMENTBARAKAT BY; ANCES IG; FAJER AB et al.1979; AMER. J. OBSTETR. GYNECOL.; USA; DA. 1979; VOL. 133; NO 4; PP. 460-461; BIBL. 2 REF.Article

PARTIAL DELETION OF THE X CHROMOSOME IN GONADAL DYSGENESIS 46,X,DEL(X)(P 22) IDENTIFIED BY BUDR TREATMENTPETRINELLI P; ANTONELLI A; GABELLINI P et al.1978; HUM. GENET.; DEU; DA. 1978; VOL. 45; NO 3; PP. 351-354; BIBL. 10 REF.Article

PARTIAL SHORT ARM DELETIONS OF THE X CHROMOSOME AND SPONTANEOUS PUBERTAL DEVELOPMENT IN GIRLS WITH SHORT STATUREKALOUSEK D; SCHIFFRIN A; BERGUER AM et al.1979; J. PEDIATR.; USA; DA. 1979; VOL. 94; NO 6; PP. 891-894; BIBL. 21 REF.Article

AN UNCOMMON PHENOTYPICAL VARIANT IN THE SHERESHEVSKY-TURNER SYNDROMEDZENIS IG; ANTIPINA NN.1979; HUM. GENET.; DEU; DA. 1979; VOL. 52; NO 3; PP. 275-279; BIBL. 15 REF.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

WOMEN HETEROZYGOUS FOR DEFICIENCY OF THE (P21->PTER) REGION OF THE X CHROMOSOME ARE FERTILE.FRACCARO M; MARASCHIO P; PASQUALI F et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 39; NO 3; PP. 283-291; BIBL. 16 REF.Article

NULLISOMY FOR THE DISTAL PORTION OF XP IN A MALE CHILD WITH A X/Y TRANSLOCATION.TIEPOLO L; ZUFFARDI O; RODEWALD A et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 39; NO 3; PP. 277-281; BIBL. 5 REF.Article

X-SHORT ARM DELETION GONADAL DYSGENESIS IN TWO SIBLINGS DUE TO UNIQUE TRANSLOCATION (XPA; 16P+).DAVIS JR; HEINE MW; LIGHTNER ES et al.1976; CLIN. GENET.; DENM.; DA. 1976; VOL. 10; NO 4; PP. 202-207; BIBL. 1 P. 1/2Article

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

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

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