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

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

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

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

An interstitial deletion of the long arm of chromosome 13ROLAND, B; LOWRY, R. B; ROBERTSON, A. S et al.Clinical genetics. 1989, Vol 35, Num 4, pp 276-281, issn 0009-9163, 6 p.Article

Molecular detection of deletions involving band q14 of chromosome 13 in retinoblastomasDRYJA, T. P; RAPAPORT, J. M; JOYCE, J. M et al.Proceedings of the National Academy of Sciences of the United States of America. 1986, Vol 83, Num 19, pp 7391-7394, issn 0027-8424Article

Localization of TDPX1, a human homologue of the yeast, thioredoxin-dependent peroxide reductase gene (TPX), to chromosome 13q12PAHL, P; BERGER, R; HART, I et al.Genomics (San Diego, Calif.). 1995, Vol 26, Num 3, pp 602-606, issn 0888-7543Article

High recombination between two physically close human basement membrane collagen genes at the distal end of chromosome 13qBOWCOCK, A. M; HEBERT, J. M; WIJSMAN, E et al.Proceedings of the National Academy of Sciences of the United States of America. 1988, Vol 85, Num 8, pp 2701-2705, issn 0027-8424Article

The gene for clotting factor 10 is mapped to 13q32→qterROYLE, N. J; FUNG, M. R; MACGILLIVRAY, R. T. A et al.Cytogenetics and cell genetics. 1986, Vol 41, Num 3, pp 185-188, issn 0301-0171Article

Trisomy 13 and myelodysplastic syndromeBEVERSTOCK, G. C; PLOEM, J. E; WESSELS, H et al.Cancer genetics and cytogenetics. 1990, Vol 48, Num 2, pp 179-182, issn 0165-4608, 4 p.Article

The gene coding for the α-chain of human propionyl-CoA carboxylase maps to chromosome band 13q32KENNERKNECHT, I; SUORMALA, T; BARBI, G et al.Human genetics. 1990, Vol 86, Num 2, pp 238-240, issn 0340-6717Article

Trisomie 13 bei einem 4 jährigen Jungen = Trisomy 13 in a four-year-old boyRAUCH, F; VAN KONINGSBRUGGEN, S; LEONARD, J. V et al.Monatsschrift für Kinderheilkunde. 1997, Vol 145, Num 5, pp 482-484, issn 0026-9298Conference Paper

Physical map around the retinoblastoma gene : possible genomic imprinting suggested by NruI digestionBLANQUET, V; TURLEAU, C; DE GROUCHY, J et al.Genomics (San Diego, Calif.). 1991, Vol 10, Num 2, pp 350-355, issn 0888-7543, 6 p.Article

Structural genes of coagulation factors VII and X located on 13q34GILGENKRANTZ, S; BRIQUEL, M.-E; ANDRE, E et al.Annales de génétique (Paris). 1986, Vol 29, Num 1, pp 32-35, issn 0003-3995Article

Integration of the physical and genetic linkage map for human chromsome 13HAWTHORN, L; COWELL, J. K.Genomics (San Diego, Calif.). 1995, Vol 27, Num 3, pp 399-404, issn 0888-7543Article

Regional localisation of tri- and tetranucleotide repeat sequence-containing cosmids on chromosome 13HAWTHORN, L. A; KAPANADSE, B; YANKOVSKY, N et al.Cytogenetics and cell genetics. 1995, Vol 70, Num 1-2, pp 102-103, issn 0301-0171Conference Paper

A trinucleotide repeat polymorphism in XT00444 (D13S635E)YANDAVA, C. N; MEYERS, V; WATKINS, H et al.Human molecular genetics (Print). 1994, Vol 3, Num 7, issn 0964-6906, p. 1209Article

A polymorphic alpha satellite sequence specific for human chromosome 13 detected by oligonucleotide primed in situ labelling (PRINS)PELLESTOR, F; GIRARDET, A; ANDREO, B et al.Human genetics. 1994, Vol 94, Num 4, pp 346-348, issn 0340-6717Article

Psychopatologische Symptomatik bei zwei Fällen partieller Trisomie 13 = Clinical pathology in two cases of partial triplication of chromosome 13SCHROÊDER, S. G; WIESBECK, G. A; HEILBRONNER, H et al.Nervenarzt. 1990, Vol 61, Num 11, pp 688-691, issn 0028-2804, 4 p.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