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

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

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

Clinical delineation of proximal and distal partial 13q trisomyROGERS, J. F.Clinical genetics. 1984, Vol 25, Num 3, pp 221-229, issn 0009-9163Article

Isolation and regional localization of DNA segments revealing polymorphic loci from human chromosome 13CAVENEE, W; LEACH, R; MOHANDAS, T et al.American journal of human genetics. 1984, Vol 36, Num 1, pp 10-24, issn 0002-9297Article

A recognizable pattern of the midface of retinoblastoma patients with interstitial deletion of 13qMOTEGI, T; KAGA, M; YANAGAWA, Y et al.Human genetics. 1983, Vol 64, Num 2, pp 160-162, issn 0340-6717Article

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

Abnormalities of chromosome 13 in myelofibrosisBORGSTROM, G. H; KNUUTILA, S; RUUTU, T et al.Scandinavian journal of haematology. 1984, Vol 33, Num 1, pp 15-21, issn 0036-553XArticle

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

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

Trisomy 13 in the child of two carriers of a 13/15 translocationMORI, M. A; HUERTAS, H; PINEL, I et al.American journal of medical genetics. 1985, Vol 20, Num 1, pp 17-20, issn 0148-7299Article

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

The phenotype in partial 13q trisomies, apropos of a familial (13;15)(q22;q26) translocationRIVAS, F; PLASCENCIA, M. L; IBARRA, B et al.Human genetics. 1984, Vol 67, Num 1, pp 86-93, issn 0340-6717Article

Ring (13),t(2;6) associated with familial fragile (16)VENTRUTO, V; RINALDI, A; RENDA, S et al.Journal of medical genetics. 1984, Vol 21, Num 3, issn 0022-2593, 233Article

The gene encoding human plasma carboxypeptidase B (CPB2) resides on chromosome 13SIAO PING TSAI; DRAYNA, D.Genomics (San Diego, Calif.). 1992, Vol 14, Num 2, pp 549-550, issn 0888-7543Article

The pathology of trisomy 13 syndrome: a study of 12 casesMOERMAN, P; FRYNS, J.-P; VAN DER STEEN, K et al.Human genetics. 1988, Vol 80, Num 4, pp 349-356, issn 0340-6717Article

Cystic hygroma and hydrops fetalis in a fetus with trisomy 13GREENBERG, F; CARPENTER, R. J; LEDRETTER, D. H et al.Clinical genetics. 1983, Vol 24, Num 5, pp 389-391, issn 0009-9163Article

Polymorphisms revealed by random probe H2-10 [D13S26] which maps to chromosome 13q21-q22BOWCOCK, A. M; HEBERT, J. M; CAVALLI-SFORZA, L. L et al.Nucleic acids research. 1988, Vol 16, Num 6, issn 0305-1048, 2745Article

Uniparental isodisomy 13 in a normal female due to transmission of a maternal t(13q13q)STALLARD, R; KRUEGER, S; JAMES, R. S et al.American journal of medical genetics. 1995, Vol 57, Num 1, pp 14-18, issn 0148-7299Article

Dinucleotide repeat polymorphism at the locus D13S231SAKSOVA, L; HENNIES, H.-C; REIS, A et al.Human molecular genetics (Print). 1993, Vol 2, Num 7, issn 0964-6906, p. 1082Article

Localization of the human tripeptidyl peptidase II gene (TPP2) to 13q32-q33 by nonradioactive in situ hybridization and somatic cell hybridsMARTINSSON, T; VUJIC, M; TOMKINSON, B et al.Genomics (San Diego, Calif.). 1993, Vol 17, Num 2, pp 493-495, issn 0888-7543Article

The Pelger-Huet anomaly: a new familial association with polydactyly and trisomy 13 syndromeBERMAN, M; FRIED, W; KNOSPE, W et al.Acta haematologica. 1983, Vol 70, Num 4, pp 275-276, issn 0001-5792Article

DEPISTAGE ECHOGRAPHIQUE DES ANOMALIES CHROMOSOMIQUES: A PROPOS DES TRISOMIES 13 ET 18AUBRY JP; AUBRY MC; HENRION R et al.1982; JOURNAL DE GENETIQUE HUMAINE; ISSN 0021-7743; CHE; DA. 1982; VOL. 30; NO 3; PP. 233-253; ABS. ENG; BIBL. 5 REF.Article

DE NOVO DUPLICATION 13Q(46,XX,DUP(13) (Q21->Q333))FRACCARO M.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 58; NO 4; PP. 444Article

A DELETED CHROMOSOME NO. 13 IN HUMAN RETINOBLASTOMA CELLS: RELEVANCE TO TUMORIGENESISBALABAN MALENBAUM G; GILBERT F; NICHOLS WW et al.1981; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1981; VOL. 3; NO 3; PP. 243-250; BIBL. 24 REF.Article