Haplotype block partition with limited resources and applications to human chromosome 21 haplotype dataKUI ZHANG; FENGZHU SUN; WATERMAN, Michael S et al.American journal of human genetics. 2003, Vol 73, Num 1, pp 63-73, issn 0002-9297, 11 p.Article

Estimating the rate of gene conversion on human chromosome 21PADHUKASAHASRAM, Badri; MARJORAM, Paul; NORDBORG, Magnus et al.American journal of human genetics. 2004, Vol 75, Num 3, pp 386-397, issn 0002-9297, 12 p.Article

Beneficial effect of 6-mercaptopurine on the mitotic index of trisomy 21 lymphocytes: implications for future researchPEETERS, M. A; LEJEUNE, J.Annales de génétique (Paris). 1989, Vol 32, Num 1, pp 21-25, issn 0003-3995, 5 p.Article

Fertility in a male with trisomy 21SHERIDAN, R; LLERENA, J. JR; MATKINS, J et al.Journal of medical genetics. 1989, Vol 26, Num 5, pp 294-298, issn 0022-2593, 5 p.Article

Human chromosome 21-encoded cDNA clonesNEVE, R. L; STEWART, G. D; NEWCOMB, P et al.Gene (Amsterdam). 1986, Vol 49, Num 3, pp 361-369, issn 0378-1119Article

Down syndrome in two siblings with 47,XY,+21 and 46,XY/46,XY,-21,+t(21q;21q)DER KALOUSTIAN, V. M; MASRI, R; KHUDR, A et al.Human genetics. 1987, Vol 75, Num 1, pp 75-97, issn 0340-6717Article

46, XX, t(15; 21)/47, XX, 15 p-, +21 mosaicism in a child with Down's syndromeLUCAS, J; LE MEE, F; PLUQUAILEC, K et al.Annales de génétique (Paris). 1986, Vol 29, Num 2, pp 104-106, issn 0003-3995Article

review and hypothesis : Akzheimer disease and down syndrome-chromosome 21 nondisjunction may underlie both disordersPOTTER, H.American journal of human genetics. 1991, Vol 48, Num 6, pp 1192-1200, issn 0002-9297, 9 p.Article

A male infant with holoprosencephaly, associated with ring chromosome 21ARONSON, D. C; JANSWEIJER, M. C. E; HOOVERS, J. M. N et al.Clinical genetics. 1987, Vol 31, Num 1, pp 48-52, issn 0009-9163Article

Regional assignment of six polymorphic DNA sequences on chromosome 21 by in situ hybridization to normal and rearranged chromosomesMUNKE, M; FOELLMER, B; WATKINS, P. C et al.American journal of human genetics. 1988, Vol 42, Num 4, pp 542-549, issn 0002-9297Article

Panel of aneuploid cell lines for physical mapping of the proximal long arm of human chromosome 21PULST, S.-M; KORENBERG, J. R.American journal of medical genetics. Supplement. 1990, Num 7, pp 137-140, issn 1040-3787, 4 p.Article

Educabilité de la mémoire immédiate de sujets normaux et sous-normaux dans deux conditions de charge mentaleVAN DAM, F; MARCQ, F; DE GANSEMAN, C et al.Psychologie et psychométrie. 1994, Vol 15, Num 1, pp 65-78, issn 0296-8770Article

Clinical aspects of Down syndrome from infancy to adulthoodPUESCHEL, S. M.American journal of medical genetics. Supplement. 1990, Num 7, pp 52-56, issn 1040-3787, 5 p.Article

Reflections on the pathogenesis of Down syndromeOPITZ, J. M; GILBERT-BARNESS, E. F.American journal of medical genetics. Supplement. 1990, Num 7, pp 38-51, issn 1040-3787, 14 p.Article

Parental age and the origin of trisomy 21: a study of 302 familiesBRICARELLI, F. D; PIERLUIGI, M; LANDUCCI, M et al.Human genetics. 1989, Vol 82, Num 1, pp 20-26, issn 0340-6717, 7 p.Article

Impact of medical genetics on public health : Down's syndromeMIKKELSEN, M.Clinical genetics. 1989, Vol 36, Num 5, issn 0009-9163, p. 337Conference Paper

Gene expression variation and expression quantitative trait mapping of human chromosome 21 genesDEUTSCH, Samuel; LYLE, Robert; ANTONARAKIS, Stylianos E et al.Human molecular genetics (Print). 2005, Vol 14, Num 23, pp 3741-3749, issn 0964-6906, 9 p.Article

Increased nondisjunction of chromosome 21 with age in human peripheral lymphocytesQINGHUA SHI; JIANFANG CHEN; ADLER, I.-D et al.Mutation research. 2000, Vol 452, Num 1, pp 27-36, issn 0027-5107Article

Educabilité de la mémoire immédiate de sujets normaux et sous-normaux dans deux conditions de charge mentaleVAN DAM, F; MARCQ, F; DE GANSEMAN, C et al.Psychologie et psychométrie. 1994, Vol 15, Num 1, pp 65-78, issn 0296-8770Article

Long-distance restriction mapping of the proximal long arm of human chromosome 21 with not I linking clonesICHIKAWA, H; SHIMIZU, K; OHKI, M et al.Proceedings of the National Academy of Sciences of the United States of America. 1992, Vol 89, Num 1, pp 23-27, issn 0027-8424Article

Epidemiology of Down syndrome in 118,265 consecutive birthsSTOLL, C; ALEMBIK, Y; DOTT, B et al.American journal of medical genetics. Supplement. 1990, Num 7, pp 79-83, issn 1040-3787, 5 p.Article

Anomalies de la fonction thyroïdienne chez les enfants trisomiques 2& = Anomalies of thyroid function in children with Down syndromeSTOLL, C; ALEMBIK, Y; DOTT, B et al.Journal de génétique humaine. 1989, Vol 37, Num 4-5, pp 389-393, issn 0021-7743, 5 p.Article

Anonymous DNA sequence from chromosome 21 showing a three allele insertion/deletion RFLP (HGM 9 provisional no. D21S82)XIAO, G.-H; GRZESCHIK, K.-H; SCHERER, G et al.Nucleic acids research. 1987, Vol 15, Num 13, issn 0305-1048, 5499Article

Identification of a Herpes Simplex Labialis Susceptibility Region on Human Chromosome 21. CommentaryKOELLE, David M; BERGEMANN, Tracy L; HOBBS, Maurine R et al.The Journal of infectious diseases. 2008, Vol 197, Num 3, issn 0022-1899, 331-334, 340-346 [11 p.]Article

Human microRNA-155 on chromosome 21 differentially interacts with its polymorphic target in the AGTR1 3' untranslated region : A mechanism for functional single-nucleotide polymorphisms related to phenotypesSETHUPATHY, Praveen; BOREL, Christelle; GAGNEBIN, Maryline et al.American journal of human genetics. 2007, Vol 81, Num 2, pp 405-413, issn 0002-9297, 9 p.Article