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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

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

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Terminal rearrangement of chromosomes 21 detected in amniotic fluid, resulting in a trisomy 21COHEN, G; MANUEL, A; COHEN, M et al.Human genetics. 1983, Vol 64, Num 2, issn 0340-6717, 203Article

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SUBREGIONAL LOCALIZATION OF THE GENE(S) GOVERNING THE HUMAN INTERFERON INDUCED ANTIVIRAL STATE IN MAN. = LOCALISATION SUB-REGIONALE DU OU DES GENES CODANT POUR L'ETAT ANTIVIRAL INDUIT PAR L'INTERFERON HUMAIN CHEZ L'HOMMETAN YH; GREENE AE.1976; J. GEN. VIROL.; G.B.; DA. 1976; VOL. 32; NO 1; PP. 153-155; BIBL. 10 REF.Article

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COPPER/ZINC SUPEROXIDE DISMUTASE (SOD-1) ACTIVITY IN REGULAR TRISOMY 21, TRISOMY 21 BY TRANSLOCATION AND MOSAIC TRISOMY 21JEZIDROWSKA A; JAKUBOWSKI L; ARMATYS A et al.1982; CLINICAL GENETICS; ISSN 0009-9163; DNK; DA. 1982; VOL. 22; NO 4; PP. 160-164; BIBL. 24 REF.Article

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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

MONOZYGOTIC TWINS DISCORDANT FOR TRISOMY 21 OR CHIMERIC DIZYGOTIC TWINS.GILGENKRANTZ S; JANOT C; ROGERS JG et al.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 15; NO 1; PP. 159-160; BIBL. 3 REF.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

PRENATAL DIAGNOSIS AND GENETIC COUNSELING IN 21 TRISOMY: ITS IMPACT ON FAMILY PLANNINGEVERS KIEBOOMS G; FRYNS JP; VAN DEN BERGHE H et al.1981; J. GENET. HUM.; ISSN 0021-7743; CHE; DA. 1981; VOL. 28; NO 5; PP. 147-159; ABS. FRE; BIBL. 12 REF.Article

SEGREGATION PREFERENTIELLE D'UN CHROMOSOME 21 P- DANS TROIS GENERATIONS: ROLE EVENTUEL DANS LA NON-DISJONCTION (A PROPOS D'UN CAS DE TRISOMIE 21 DANS CETTE FAMILLE)DE LOS COBOS L; LIGIA AP.1981; J. GENET. HUM.; ISSN 0021-7743; CHE; DA. 1981; VOL. 28; NO 5; PP. 201-206; ABS. ENG; BIBL. 14 REF.Article