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Results 1 to 25 of 276586

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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

ORIGIN OF A SMALL METACENTRIC CHROMOSOME: FAMILIAL AND CYTOGENETIC EVIDENCE = ORIGINE D'UN PETIT CHROMOSOME METACENTRIQUE: PREUVE FAMILIALE CYTOGENETIQUETAYLOR KM; WOLFINGER HL; BROWN MG et al.1975; CLIN. GENET.; DENM.; DA. 1975; VOL. 8; NO 5; PP. 364-369; BIBL. 11 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

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

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

CYTOGENETICS OF 50 PATIENTS WITH MENTAL RETARDATION AND MULTIPLE CONGENITAL ANOMALIES AND 50 NORMAL SUBJECTS. MADISON BLIND STUDY IVMAGNELLI NC.1976; CLIN. GENET.; DENM.; DA. 1976; VOL. 9; NO 2; PP. 169-182; BIBL. 23 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

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

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

CHROMOSOME MEASUREMENTS ON AN XXP+MALEKAMLESH MADAN.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 32; NO 2; PP. 141-142; BIBL. 5 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

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

TRISOMIE 4P DE NOVO PAR ISOCHROMOSOME 4P.ANDRE MJ; AURIAS A; DE BERRANGER P et al.1976; ANN. GENET.; FR.; DA. 1976; VOL. 19; NO 2; PP. 127-131; ABS. ANGL.; BIBL. 16 REF.Article

IDENTIFICATION DE DEUX TRANSLOCATIONS FAMILIALESLAURENT C; BIEMONT MC; ROBERT JM et al.1974; SEM. HOP., ANN. GENET.; FR.; DA. 1974; VOL. 17; NO 4; PP. 279-281; ABS. ANGL.; BIBL. 8REF.Serial Issue

AN UNUSUAL CHROMOSOMAL SEGREGATION IN A FAMILY WITH A TRANSLOCATION BETWEEN CHROMOSOMES 3 AND 12 = SEGREGATION CHROMOSOMIQUE INHABITUELLE DANS UNE FAMILLE CONDUCTRICE D'UNE TRANSLOCATION ENTRE LES CHROMOSOMES 3 ET 12SACHDEVA S; SMITH GF; JUSTICE P et al.1974; J. MED. GENET.; G.B.; DA. 1974; VOL. 11; NO 3; PP. 303-305; BIBL. 4 REF.Article

TYPE AND CONTRETYPE SIGNS IN MONOSOMY AND TRISOMY 9P: ON A CASE 46,XY,DEL(9) (PTER->P12:)HERNANDEZ A; RIVERA H; JIMENEZ SAINZ M et al.1979; ANN. GENET.; FRA; DA. 1979; VOL. 22; NO 3; PP. 155-157; ABS. FRE; BIBL. 13 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

AUTOSOMALE CHROMOSOMENABERRATIONEN = ABERRATIONS AUTOSOMIQUESSCHINZEL A.1979; ARCH. GENET.; CHE; DA. 1979; VOL. 52; NO 1-2; 204 P.; ABS. ENG; BIBL. 53 REF.Serial Issue

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

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

CYTOGENETIC DISORDERS.1976; BIRTH DEFECTS ORIGIN. ATRICLE SER.; U.S.A.; DA. 1976; VOL. 12; NO 5; PP. 87-177; BIBL. DISSEM.; (CYTOGENET. ENVIRON. MALFORM. SYNDROMES. CONF.; KANSAS CITY, MO.; 1975)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

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

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

NEW AUTOSOMAL SYNDROMES: TRISOMIES 4 P AND 9 P.DALLAPICCOLA B; MASTROIACOVO P; SEGNI G et al.1977; ACTA GENET. MED. GEMELLOL.; ITAL.; DA. 1977; VOL. 26; NO 3-4; PP. 267-273; ABS. ITAL. FR. ALLEM.; BIBL. 9 REF.Article

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