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DIFFERENCIATION, D'APRES LEUR LONGUEUR, DES CHROMOSOMESX DANS LA POLYSOMIEX, CHEZ L'HOMMEBARANOVSKAYA LI.1973; BJULL. EKSPER. BIOL. MED.; S.S.S.R.; DA. 1973; VOL. 75; NO 2; PP. 94-98; ABS. ANGL.; BIBL. 12REF.Serial Issue

XXXX SYNDROME: CASE REPORT, AND A NOTE ON GENETIC COUNSELLING AND FERTILITY = SYNDROME XXXX: OBSERVATION D'UN CAS ET NOTE SUR LE CONSEIL GENETIQUE ET LA FERTILITEGARDNER RJM; VEALE AMO; SANDS VE et al.1972; HUMANGENETIK; DTSCH.; DA. 1972; VOL. 17; NO 4; PP. 323-330; ABS. ALLEM.; BIBL. 1P.Serial Issue

ROKITANSKY-KUESTER-HAUSER SYNDROME ASSOCIATED WITH A VERY RARE XO/XX/XXX/XXXX/XXXXX CHROMOSOMAL MOSAICISMDOKUMOV SI; SPASOV SA; GENKOVA PI et al.1972; INTERNATION. J. GYNAECOL. OBSTETR.; U.S.A.; DA. 1972; VOL. 10; NO 6; PP. 250-255; ABS. FR.; BIBL. 7 REF.Article

EIN FALL VON X-TETRASOMIE (48, XXXX = UN CAS DE TETRASOMIE 48, XXXXWAGENBICHLER P; GOLOB E; SZILVASSY J et al.1973; WIEN. KLIN. WSCHR.; OESTERR.; DA. 1973; VOL. 85; NO 1; PP. 5-10; ABS. ANGL.; BIBL. 18 REF.Article

DIFFERENCIATION DES CHROMOSOMES X PAR LES METHODES DE DESPIRALISATION AU 5-BROMODEOXYURIDINE (BUDR) ET DE DENATURATION THERMIQUE MENAGEEBARANOVSKAYA LT; ZAKHAROV AF; DUTRILLAUX B et al.1972; SEM. HOP., ANN. GENET.; FR.; DA. 1972; VOL. 15; NO 4; PP. 271-274; ABS. ANGL.; BIBL. 9REF.Serial Issue

H3-DEOXYCYTIDINE INCORPORATION INTO X-CHROMOSOMES DIFFERENTIALLY CONDENSED UNDER 5-BROMODEOXYURIDINE TREATMENT IN CASES OF 49,XXXXY, 48,XXXX, 47,XXX, 46,X,I(XQ), AND 45,X46, XI(XQ) = INCORPORATION DE LA DESOXYCYTIDINE-H3 DANS LES CHROMOSOMES X CONDENSES DE FACON DIFFERENTIELLE SOUS TRAITEMENT PAR LA 5-BROMODESOXYURIDINE DANS DES CAS DE 49,XXXXY, 48,XXXX, 47,XXX, 46,X,I(XQ) ET 45,X/46,X,I(XQ)BARANOVSKAYA LI; ZAKHAROV AF.1974; HUMAGENETIK; DTSCH.; DA. 1974; VOL. 23; NO 2; PP. 131-136; ABS. ALLEM.; BIBL. 15 REF.Article

LE SYNDROME 48, XXXXDE GROUCHY J; VIALATTE J; CHAVIN COLIN F et al.1979; ARCH. FR. PEDIATR.; FRA; DA. 1979 PUBL. 1980; VOL. 36; SUPPL. 1; PP. XLI-XLVII; ABS. ENG; BIBL. 28 REF.Article

CONGENITAL HEART DISEASE IN A TETRA-X WOMAN = CARDIOPATHIE CONGENITALE CHEZ UNE FEMME TETRA-XKEANE JF; MCLENNAN JE; CHI JG et al.1974; CHEST; U.S.A.; DA. 1974; VOL. 66; NO 6; PP. 726-729; BIBL. 21REF.Article

A TETRA-X FEMALE: CYTOGENETIC TESTING, DERMATOGLYPHIC STUDIES, AND SPEECH IMPAIRMENTHOWARD PEEBLES PN; MARKITON RI.1979; AMER. J. MENTAL DEFIC.; USA; DA. 1979; VOL. 84; NO 3; PP. 252-255; BIBL. 11 REF.Article

THE 49 XXXXX SYNDROME. REPORT OF A CASE WITH 48 XXXX/49 XXXXX MOSAICISMSILENGO MC; DAVI GF; FRANCESCHINI P et al.1979; ACTA PAEDIATR. SCAND.; SWE; DA. 1979; VOL. 68; NO 5; PP. 769-771; BIBL. 14 REF.Article

ANOMALIE CHROMOSOMIQUE RARE: TETRASOMIE X (48 XXXX)PASCALIS G; BAJOLLE F; DELPECH J et al.1980; ANN. MEDICO-PSYCHOL.; FRA; DA. 1980; VOL. 138; NO 3; PP. 297-303; ABS. ENG; BIBL. 8 REF.Article

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