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Results 1 to 25 of 77854

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RED BLOOD CELL GLUTATHIONE PROXIDASE IN SIMPLE TRISOMY 21 AND TRANSLOCATION 21/22KEDZIORA J; LUKASZEWICZ R; KOTER M et al.1982; EXPERIENTIA; ISSN 0014-4754; CHE; DA. 1982; VOL. 38; NO 5; PP. 543-544; BIBL. 20 REF.Article

Double trisomie et inversion péricentrique transmise [48,XXY, +21, inv(22)] effet interchrosomique = Double trisomy and inherited pericentric inversion [48,XXY, +21, inv(22)] interchromosomal effectSAURA, R; LONGY, M; SAUTAREL, M et al.Annales de génétique (Paris). 1983, Vol 26, Num 3, pp 180-182, issn 0003-3995Article

THREE INTERESTING CASES OF DOWN SYNDROMEPEREZ CASTILLO A; DEL MAZO J; ABRISQUETA JA et al.1983; ANNALES DE GENETIQUE; ISSN 0003-3995; FRA; DA. 1983; VOL. 26; NO 2; PP. 123-128; ABS. FRE; BIBL. 24 REF.Article

INTERFERON EFFECT ON RIBOSOMAL RIBONUCLEIC ACID RELATED TO CHROMOSOME 21 PLOIDYMAROUN LE.1979; BIOCHEM. J.; GBR; DA. 1979; VOL. 179; NO 1; PP. 221-225; BIBL. 18 REF.Article

FIVE UNUSUAL KARYOTYPES IN DOWN'S SYNDROMECASALONE R; FRACCARO M; FRANCESCONI D et al.1979; ANN. GENET.; FRA; DA. 1979; VOL. 22; NO 1; PP. 17-20; ABS. FRE; BIBL. 15 REF.Article

FOUR NEW CASES OF RING 21 AND 22 INCLUDING FAMILIAL TRANSMISSION OF RING 21.PALMER CG; HODES ME; REED T et al.1977; J. MED. GENET.; G.B.; DA. 1977; VOL. 14; NO 1; PP. 54-60; BIBL. 1 P.Article

CONTRIBUTION A L'ETUDE DE LA CARTE FACTORIELLE DU CHROMOSOME 21 D'APRES 1 OBSERVATION DE MONOSOMIE 21 PARTIELLE ET 1 OBSERVATION DE TRISOMIE 21 PARTIELLECOTTONI DURAND MARTINE.sd; FRA; DA. S.D.; 130; 106 P.: ILL.; 30 CM; BIBL. 20 P.; TH.: MED./NANCY I/1979Thesis

I/21 TRANSLOCATION.MILLER JQ; WILLSON K; GOLDBERG MJ et al.1977; SOUTH. MED. J.; U.S.A.; DA. 1977; VOL. 70; NO 1; PP. 102-104; BIBL. 6 REF.Article

Mosaic down's syndrome with de novo 45, XX, -21, -22, +t(21q; 22q)/46, XX, -21, +t(21q:21q) rearrangementTHARAPEL, A. T; REDHEENDRAN, R; MANKINEN, B et al.Journal of medical genetics. 1984, Vol 21, Num 5, pp 391-395, issn 0022-2593Article

In situ hybridization and translocation breakpoint mapping. II: Two unusual T(21; 22) translocationsCANNIZZARO, L. A; ARONSO, M. M; EMANUEL, B. S et al.Cytogenetics and cell genetics. 1985, Vol 39, Num 3, pp 173-178, issn 0301-0171Article

HUMAN ACROCENTRIC RING CHROMOSOMES AND SATELLITE ASSOCIATION.CANTU JM; SALAMANCA F; SANCHEZ J et al.1975; ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 3; PP. 193-196; ABS. FR.; BIBL. 23 REF.Article

DOWN'S SYNDROME PHENOTYPE AND AUTOSOMAL GENE INACTIVATION IN A CHILD WITH PRESUMED (X;21) DE NOVO TRANSLOCATIONTAYSI K; SPARKES RS; O'BRIEN TJ et al.1982; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1982; VOL. 19; NO 2; PP. 144-148; BIBL. 15 REF.Article

DIC (21;21) IN A DOWN'S SYNDROME CHILD WITH AN UNUSUAL CHROMOSOME 9 VARIANT IN THE MOTHERBERG JM; GARDNER HA; GARDNER RJM et al.1980; J. MED. GENET.; GBR; DA. 1980; VOL. 17; NO 2; PP. 144-148; BIBL. 9 REF.Article

CHYLOTHORAX IN TWO MONGOLOID INFANTS.YOSS BS; LIPSITZ PJ.1977; CLIN. GENET.; DENM.; DA. 1977; VOL. 12; NO 6; PP. 357-360; BIBL. 9 REF.Article

CARYOTYPE 45,XY-18-21, +T(18;21) (18 Q TER->CEN->21 Q TER) CHEZ UN NOURRISSON.SERVILLE F; FONTAN D; BROUSTET A et al.1977; BORDEAUX MED.; FR.; DA. 1977; VOL. 10; NO 18; PP. 1227-1230; BIBL. 4 REF.Article

DOWN'S SYNDROME ASSOCIATED WITH FAMILIAL 21P+ VARIANTKLECZKOWSKA A; KUBIEN E.1981; GENET. POL.; ISSN 0016-6715; POL; DA. 1981; VOL. 22; NO 1; PP. 113-115; ABS. POL/RUS; BIBL. 11 REF.Article

PARTIAL MONOSOMY 13 AND 21 DUE TO A FAMILIAL 13/21 TRANSLOCATION.GUIMARAES OTTO P; TOLEDO S; RICHIERI COSTA A et al.1978; HUM. GENET.; GERM.; DA. 1978; VOL. 41; NO 3; PP. 243-250; BIBL. 11 REF.Article

LE RISQUE DE TRISOMIE 21 DANS LA DESCENDANCE EN CAS DE TRANSLOCATION MATERNELLE T (7; 21).GIRAUD F; MATTEI JF; MATTEI MG et al.1977; NOUV. PRESSE MED.; FR.; DA. 1977; VOL. 6; NO 14; PP. 1233; BIBL. 1 REF.Article

DOUBLE ANEUPLOIDY: PARTIAL TRISOMY 21 AND XO/XXX IN A FAMILY WITH 12/21 TRANSLOCATIONCHEN H; TYRKUS M; WOOLLEY PV et al.1978; ANN. GENET.; FRA; DA. 1978; VOL. 21; NO 3; PP. 177-180; ABS. FRE; BIBL. 17 REF.Article

TWO CASES OF TRISOMY 12P DUE TO 2CPT (12; 21) (P11; P11) INHERITED THROUGH THREE GENERATIONSPARSLOW M; CHAMBERS D; DRUMMOND M et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 47; NO 3; PP. 253-260; BIBL. 18 REF.Article

SINDROME 18P - DA TRASLOCAZIONE 18/21 = SYNDROME 18P - PAR TRANSLOCATION 18/21FERRANTE E; CHESSA L; BRUNI L et al.1979; MINERVA PEDIATR.; ITA; DA. 1979; VOL. 31; NO 8; PP. 657-664; ABS. ENG; BIBL. 2 P.Article

PARTIAL TRISOMY 18Q IN A NEWBORN WITH TYPICAL 18 TRISOMY PHENOTYPEFRYNS JP; DETAVERNIER F; VAN FLETEREN A et al.1978; HUM. GENET.; DEU; DA. 1978; VOL. 44; NO 2; PP. 201-205; BIBL. 11 REF.Article

DOWN'S SYNDROME WITH 45 CHROMOSOMESLURIE IW.1979; HUM. GENET.; DEU; DA. 1979; VOL. 46; NO 1; PP. 121-123; BIBL. 3 REF.Article

A (6;21) TRANSLOCATION, UNBALANCED, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO GM-144BORGAONKAR DS; GREENE AE; CORIELL LL et al.1974; CYTOGENET. CELL GENET.; SWITZ.; DA. 1974; VOL. 13; NO 4; PP. 403-405; BIBL. 3 REF.Article

LES TRISOMIQUES 211982; READAPTATION; ISSN 0484-0305; FRA; DA. 1982; NO 295; PP. 3-36; BIBL. DISSEM.Article

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