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

Ring chromosome 21 in a normal femaleKLECZKOWSKA, A; FRYNS, J. P.Annales de génétique (Paris). 1984, Vol 27, Num 2, pp 126-128, issn 0003-3995Article

Isochromosome 21 and other chromosomal abnormalities in a patient with erythroleukaemiaWERNER-FAVRE, C; CABROL, C; BERIS, P et al.Annales de génétique (Paris). 1983, Vol 26, Num 4, pp 240-242, issn 0003-3995Article

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

Ring chromosome 21 in phenotypically apparently normal persons: report of two families from Switzerland and ItalySCHMID, W; TENCONI, R; BACCICHETTI, C et al.American journal of medical genetics. 1983, Vol 16, Num 3, pp 323-329, issn 0148-7299Article

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

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

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 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

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

Ring chromosome 21: observation in a female infantCARLO STELLA, N; BARBERI, I; CORRADO, F et al.Annales de génétique (Paris). 1984, Vol 27, Num 4, pp 249-251, issn 0003-3995Article

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

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

MONOSOMIA PARZIALE DI UN CROMOSOMA DEL GRUPPO G (21 Q-) ASSOCIATA A NANISMO MESOMELICO A TRASMISSIONE AUTOSOMICA DOMINANTE. = MONOSOMIE PARTIELLE D'UN CHROMOSOME DU GROUPE G (21 Q-)-ASSOCIEE A UN MANISME MESOMELIQUE A TRANSMISSION AUTOSOMIQUE DOMINANTEDUILLO MT.1977; MINERVA PEDIATR.; ITAL.; DA. 1977; VOL. 29; NO 21; PP. 1341-1348; ABS. ANGL.; BIBL. 1 P.Article

DE NOVO APPEARANCE OF A TRANSLOCATION T(5P; 21Q), AND ITS TRANSMISSION IN BOTH BALANCED AND UNBALANCED FORMS TO THE NEXT GENERATIONCHAGANTI RSK; MORILLO CUCCI G; FRIIS L et al.1976; ANN. GENET.; FR.; DA. 1976; VOL. 19; NO 1; PP. 43-48; ABS. FR.; BIBL. 23 REF.Article

TRANSLOCATION (13Q21Q). FOUR GENERATION FAMILY STUDY WITH ANALYSIS OF SATELLITE ASSOCIATIONS, FLOURESCENT MARKERS, AND PRENATAL DIAGNOSIS. = TRANSLOCATION (13Q21Q). ETUDE FAMILIALE SUR QUATRE GENERATIONS AVEC ANALYSE DES ASSOCIATIONS DE SATELLITES, DES MARQUEURS FLUORESCENTS ET DIAGNOSTIC ANTENATALMIKKELSEN M; HANSSON A; JACOBSEN P et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 27; NO 4; PP. 303-307; BIBL. 4 REF.Article