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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

A (4;21) TRANSLOCATION, UNBALANCED, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO. GM-98SEABRIGHT M; MILLER RC; GREENE AE et al.1975; CYTOGENET. CELL GENET.; SWITZ.; DA. 1975; VOL. 14; NO 2; PP. 152-153Article

TRISOMIE 21 PARTIELLE (21Q21->21Q22.2)POISSONNIER M; SAINT PAUL B; DUTRILLAUX B et al.1976; ANN. GENET.; FR.; DA. 1976; VOL. 19; NO 1; PP. 69-73; ABS. ANGL.; BIBL. 12 REF.Article

FAMILIAL 21/22 TRANSLOCATIONPAPP Z; DOLHAY B; GARDO S et al.1975; ACTA GENET. MED. GEMELLOL.; ITAL.; DA. 1975; VOL. 24; NO 1-2; PP. 69-73; ABS. ITAL. FR. ALLEM.; BIBL. 18 REF.Article

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

TOPOLOGICAL FORMULATION OF FINGER-TIP PATTERNS: COMPARISON OF COMPLETE AND INCOMPLETE 21 TRISOMICS WITH NORMAL SUBJECTS = FORMULATION TOPOLOGIQUE DES EMPREINTES DIGITALES: COMPARAISON DES TRISOMIQUES 21 COMPLETS ET INCOMPLETS AVEC LES SUJETS NORMAUXLOESCH D.1975; J. MENTAL DEFIC. RES.; G.B.; DA. 1975; VOL. 19; NO 2; PP. 121-137; BIBL. 14 REF.Article

A FAMILY WITH AN INHERITED TRANSLOCATION INVOLVING THE NO 4/NO. 21 CHROMOSOMESDARMADY JM; SEABRIGHT M.1975; J. MED. GENET.; G.B.; DA. 1975; VOL. 12; NO 4; PP. 408-411; BIBL. 9 REF.Article

THREE GENERATIONS AND SEVEN FAMILY MEMBERS WITH A T(21Q22Q) CHROMOSOME = CHROMOSOME T(21Q22Q) CHEZ SEPT MEMBRES D'UNE FAMILLE SUR TROIS GENERATIONSZERGOLLERN L.1974; J. MED. GENET.; G.B.; DA. 1974; VOL. 11; NO 4; PP. 379-381; BIBL. 5REF.Article

A case of 21q: syndrome with half normal SOD-1 activityYOSHIMITSU, K; HATANO, S; KOBAYASHI, Y et al.Human genetics. 1983, Vol 64, Num 2, pp 200-202, issn 0340-6717Article

INTERSTITIAL DELECTION OF CHROMOSOME 21MODI N; BUCKTON KE.1982; CLINICAL GENETICS; ISSN 0009-9163; DNK; DA. 1982; VOL. 22; NO 4; PP. 215-219; BIBL. 28 REF.Article

A CASE OF R(21) WITH STIGMATA OF ATYPICAL DOWN SYNDROMEIESHIMA A; OGA SAWARA N; YAMAMOTO Y et al.1980; HUM. GENET.; DEU; DA. 1980; VOL. 55; NO 1; PP. 65-69; BIBL. 18 REF.Article

Q-: A CANDIDATE CHROMOSOME MARKER OF PRIMARY THROMBOCYTHEMIAZACCARIA A; BACCARANI M; GUGLIOTTA L et al.1978; HAEMATOLOGICA; ITA; DA. 1978; VOL. 63; NO 3; PP. 337-338; BIBL. 6 REF.Article

CONTRIBUTION A L'ETUDE DE LA TRISOMIE 21 PARTIELLE. A PROPOS DE 3 CAS.GERBAUD CENNI D.1978; MARSEILLE; ASSOC. ANCIENS EXTERNES HOP.; DA. 1978; PP. 1-53; H.T. 15; BIBL. 5 P. 1/2; (THESE DOCT. MED.; PARIS V)Thesis

A THREE CHROMOSOME TRANSLOCATION INVOLVING TWO HOMOLOGOUS CHROMOSOMES IN A TRISOMIE ABORTUSCREASY MR; CROLLA JA; POLANI PE et al.1976; CLIN. GENET.; DENM.; DA. 1976; VOL. 9; NO 1; PP. 15-19; BIBL. 1 P.Article

TRISOMY 10P. A REPORT OF TWO CASES DUE TO A FAMILIAL TRANSLOCATION RCP (10; 21) (P 11; P 11)CANTU JM; SALAMANCA F; BUENTELLO L et al.1975; SEM. HOP., ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 1; PP. 5-11; ABS. FR.; BIBL. 20REF.Article

MATERNALLY TRANSMITTED EXTRA RING (21) CHROMOSOME IN A BOY WITH DOWN'S SYNDROMEMATSUBARA T; NAKAGOME Y; OGASAWARA N et al.1982; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1982; VOL. 60; NO 1; PP. 78-79; BIBL. 12 REF.Article

ZUR AETIOLOGIE DES MONGOLISMUS = L'ETIOLOGIE DU MONGOLISMEWAGENBICHLER P.1981; NATURWISSENSCHAFTEN; ISSN 0028-1042; DEU; DA. 1981; VOL. 68; NO 2; PP. 76-81; ABS. ENG; BIBL. 40 REF.Article

TRISOMIE 21 PAR DUPLICATION EN MIROIR 46, XX, PSU DIC(21) TER REA (21 Q 21 Q)TURLEAU C; ROUBIN M; CHAVIN COLIN F et al.1980; ANN. GENET.; FRA; DA. 1980; VOL. 23; NO 3; PP. 187-189; ABS. ENG; BIBL. 19 REF.Article

A CHROMOSOMAL ABNORMALITY (219) IN PRIMARY THROMBOCYTOSISPETIT P; VANDEN BERGHE H.1979; HUM. GENET.; DEU; DA. 1979; VOL. 50; NO 1; PP. 105-106; BIBL. 1 REF.Article

A CASE OF ATYPICAL DOWN'S SYNDROME WITH MOSAIC 46, XX/46, XX-21+T(21Q21Q).HORNSTEIN L; SOUKUP S.1976; CLIN. GENET.; DENM.; DA. 1976; VOL. 10; NO 2; PP. 77-81; BIBL. 22 REF.Article

FAMILIAL NEUROBLASTOMAPEGELOW CH; EBBIN AJ; POWARS D et al.1975; J. PEDIATR.; U.S.A.; DA. 1975; VOL. 87; NO 5; PP. 763-765; BIBL. 15 REF.Article

TRISOMY 4G32->4GTER DUE TO A MATERNAL 4/21 TRANSLOCATIONBACCICHETTI C; TENCONI R; ANGLANI F et al.1975; J. MED. GENET.; G.B.; DA. 1975; VOL. 12; NO 4; PP. 425-427; BIBL. 9 REF.Article

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

21Q-IN PRIMARY THROMBOCYTHEMIAZACCARIA A; BACCARANI M; GUGLIOTTA L et al.1980; CANCER GENET. CYTOGENET.; USA; DA. 1980; VOL. 1; NO 4; PP. 337-344; BIBL. 33 REF.Article

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

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