RING CHROMOSOME 13 IN A POLYMALFORMED ANENCEPHALIC = CHROMOSOME 13 EN ANNEAU CHEZ UN ANENCEPHALE POLYMALFORMESCHMID W; MUEHLETHALER JP; BRINER J et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 27; NO 1; PP. 63-66; BIBL. 6REF.Article

CHROMOSOME 13 EN ANNEAUHEVIA A; BULLON M; NOVALES A et al.1979; ANN. GENET.; FRA; DA. 1979; VOL. 22; NO 4; PP. 232-233; ABS. ENG; BIBL. 7 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

A CASE OF D₁₃ RING CHROMOSOMECOSSU P; DIANA G; MAMELI M et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 46; NO 1; PP. 111-114; BIBL. 10 REF.Article

RING CHROMOSOME 13 IN A CHILD WITH MINOR DYSMORPHIC FEATURES, IRREGULAR PHENOTYPIC EXPRESSION OF RING 13 SYNDROMEVERMA RS; DOSIK H; CHOWDHRY IH et al.1978; AMER. J. DIS. CHILD; USA; DA. 1978; VOL. 132; NO 10; PP. 1018-1021; BIBL. 21 REF.Article

IRREGULAR PHENOTYPIC EXPRESSION OF RING CHROMOSOMES = EXPRESSION PHENOTYPIQUE IRREGULIERE DES CHROMOSOMES ANNULAIRESZDANSKY R; ANDRLE M; BUEHLER E et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 26; NO 3; PP. 193-198; ABS. ALLEM.; BIBL. 14REF.Article

PARENTAL ORIGIN OF A RING 13 CHROMOSOME IN A FEMALE WITH MULTIPLE ANOMALIES.MAGENIS RE; WYANDT HE; OVERTON KM et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 33; NO 2; PP. 181-186; BIBL. 9 REF.Article

The DNA sequence and analysis of human chromosome 13DUNHAM, A; MATTHEWS, L. H; JONES, M. C et al.Nature (London). 2004, Vol 428, Num 6982, pp 522-528, issn 0028-0836, 7 p.Article

LONG SURVIVAL IN TRISOMY-13-SYNDROME: 21 CASES INCLUDING PROLONGED SURVIVAL IN TWO PATIENTS 11 AND 19 YERS OLDREDHEENDRAN R; NEU RL; BANNERMAN RM et al.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 8; NO 2; PP. 167-172; BIBL. 7 REF.Article

PERICENTRIC INVERSION OF CHROMOSOME NO. 13 IN A LARGE FAMILY LEADING TO DUPLICATION DEFICIENCY CAUSING CONGENITAL MALFORMATIONS IN THREE INDIVIDUALS = INVERSION PERICENTRIQUE DU CHROMOSOME NO13 DANS UNE IMPORTANTE FAMILLE CONDUISANT A UNE DUPLICATION AVEC DEFICIT CAUSE DE MALFORMATIONS CONGENITALES CHEZ TROIS INDIVIDUSHAUKSDOTTIR H; HALLDORSSON S; JENSSON O et al.1972; J. MED. GENET.; G.B.; DA. 1972; VOL. 9; NO 4; PP. 413-421; BIBL. 10REF.Serial Issue

A DOUBLE ANEUPLOID MOSAIC: TRISOMY 13 AND XXY = MOSAIQUE ANEUPLOIDE DOUBLE AVEC TRISOMIE 13 ET XXYEBBIN AJ; CHU LIM R; TOWNER JW et al.1972; J. MED. GENET.; G.B.; DA. 1972; VOL. 9; NO 3; PP. 365-367; BIBL. 1 REF.Serial Issue

D1 RING CHROMOSOME IN NEWBORN WITH PECULIAR FACE, POLYDACTYLY, IMPERFORATE ANUS, ARRHINENCEPHALY, AND OTHER MALFORMATIONS = CHROMOSOME D1 EN ANNEAU CHEZ UN NOUVEAU-NE AVEC FACIES PARTICULIER, POLYDACTYLIE, IMPERFORATION ANALE, ARRHINENCEPHALIE ET D'AUTRES MALFORMATIONSBILES AR JR; LUEERS T; SPERLING K et al.1970; J. MED. GENET.; G.B.; DA. 1970; VOL. 7; NO 4; PP. 399-401; BIBL. 17 REF.Serial Issue

Localization of the human homologue of the Drosophila dachshund gene (DACH) to chromosome 13q21KOZMIK, Z; CVEKL, A.Genomics (San Diego, Calif.). 1999, Vol 59, Num 1, pp 110-111, issn 0888-7543Article

Assignment of the human GAS6 gene to chromosome 13q34 by fluorescence in situ hybridizationSACCONE, S; MARCANDALLI, P; GOSTISSA, M et al.Genomics (San Diego, Calif.). 1995, Vol 30, Num 1, pp 129-131, issn 0888-7543Article

RING CHROMOSOME 13 AND HAPTOGLOBIN HETEROZYGOSITY = CHROMOSOME 13 ANNULAIRE ET HETEROZYGOTIE POUR L'HAPTOGLOBINEFITZGERALD PH.1973; CLIN. GENET.; DANM.; DA. 1973; VOL. 4; NO 1; PP. 25-27; BIBL. 12REF.Serial Issue

GENETIC MARKERS IN TRISOMIES 13 AND 18COTE GB; EDWARDS JH.1976; ANN. HUM. GENET.; G.B.; DA. 1976; VOL. 39; NO 3; PP. 335-337; BIBL. 3 REF.Article

MALFORMATIVE SYNDROME WITH RING CHROMOSOME 13 = SYNDROME MALFORMATIF AVEC CHROMOSOME 13 EN ANNEAU)FRYNS JP; DEROOVER J; VAN DEN BERGHE H et al.1974; HUMANGENETIK; DTSCH.; DA. 1974; VOL. 24; NO 3; PP. 235-240; BIBL. 4REF.Article

THE BEHAVIOR OF RING CHROMOSOME 13 = LE COMPORTEMENT DU CHROMOSOME 13 ANNULAIREHOO JJ; OBERMANN U; CRAMER H et al.1974; HUMANGENETIK; DTSCH.; DA. 1974; VOL. 24; NO 3; PP. 161-171; ABS. ALLEM.; BIBL. 16REF.Article

Interstitial deletion of long arm of chromosome 13CARNEVALE, A; FRIAS, S; ALCANTAR, R et al.Annales de génétique (Paris). 1984, Vol 27, Num 1, pp 49-52, issn 0003-3995Article

THE RING CHROMOSOME 13 SYNDROMEMARTIN NJ; HARVEY PJ; PEARN JH et al.1982; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1982; VOL. 61; NO 1; PP. 18-23; BIBL. 23 REF.Article

A(13) TERMINAL DELETION, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO. GM-250.ARONSON M; ZACKAL E; MELLMAN W et al.1975; CYTOGENET. CELL GENET.; SWITZ.; DA. 1975; VOL. 15; NO 1; PP. 57-58Article

UNUSUAL 13/13 TRANSLOCATION AND 13 TRISOMY PHENOTYPEFRYNS JP; KLECZKOWSKA A; KUBIEN E et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 2; PP. 113-115; ABS. FRE; BIBL. 5 REF.Article

RATES OF 47, +13 AND 46 TRANSLOCATION D/13 PATAU SYNDROME IN LIVE BIRTHS AND COMPARISON WITH RATES IN FETAL DEATHS AND AT AMNIOCENTESISHOOK EB.1980; AM. J. HUM. GENET.; ISSN 0002-9297; USA; DA. 1980; VOL. 32; NO 6; PP. 849-858; BIBL. 33 REF.Article

D₁₃ RING CHROMOSOME SYNDROME. = SYNDROME DU CHROMOSOME D13 EN ANNEAUMCCANDLESS A; WALKER S.1976; ARCH. DIS. CHILDH.; G.B.; DA. 1976; VOL. 51; NO 6; PP. 449-453; BIBL. 20 REF.Article

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21BLOUIN, J.-L; DOMBROSKI, B. A; LAMACZ, M et al.Nature genetics. 1998, Vol 20, Num 1, pp 70-73, issn 1061-4036Article