Fri. Oct 11th, 2024

Maturation delay, retardation of development, and cortical dysgenesis. Am J Med
Maturation delay, retardation of growth, and cortical dysgenesis. Am J Med Genet Suppl 1990, 7:27481. Takashima S, Iida K, Mito T, Arima M: Dendritic and histochemical development and ageing in sufferers with Down’s syndrome. J Intellect Disabil Res 1994, 38(Pt three):26573. Pritchard MA, Kola I: The “gene dosage effect” hypothesis versus the “amplified developmental instability” hypothesis in Down syndrome. J Neural Transm Suppl 1999, 57:29303. Delabar JM, Theophile D, Rahmani Z, Chettouh Z, Blouin JL, Prieur M, Noel B, Sinet PM: Molecular mapping of twenty-four features of Down syndrome on chromosome 21. Eur J Hum Genet 1993, 1:11424. Lyle R, B a F, Gagos S, Gehrig C, Lopez G, Schinzel A, Lespinasse J, Bottani A, Dahoun S, Taine L, Doco-Fenzy M, Cornillet-Lef vre P, Pelet A, Lyonnet S, Toutain A, Colleaux L, Horst J, Kennerknecht I, Wakamatsu N, Descartes M, Franklin JC, Florentin-Arar L, Kitsiou S, A Yahya-Graison E, Costantine M, Sinet P-M, Delabar JM, Antonarakis SE: Genotype-phenotype correlations in Down syndrome identified by array CGH in 30 situations of partial trisomy and partial monosomy chromosome 21. Eur J Hum Genet 2009, 17:45466. Olson LE, Richtsmeier JT, Leszl J, Reeves RH: A chromosome 21 critical region does not trigger certain Down syndrome phenotypes. PI3KC2β supplier Science 2004, 306:68790. Korbel JO, Tirosh-Wagner T, Urban AE, Chen X-N, Kasowski M, Dai L, Grubert F, Erdman C, Gao MC, Lange K, Sobel EM, Barlow GM, Aylsworth AS, Carpenter NJ, Clark RD, Cohen MY, Doran E, Falik-Zaccai T, Lewin SO, Lott IT, McGillivray BC, Moeschler JB, Pettenati MJ, Pueschel SM, Rao KW, Shaffer LG, Shohat M, Van Riper AJ, Warburton D, Weissman S, et al: The genetic architecture of Down syndrome phenotypes revealed by high-resolution evaluation of human segmental trisomies. Proc Natl Acad Sci USA 2009, 106:120312036. Deitz SL, Blazek JD, Solzak JP, Roper RJ: Down Syndrome: A Complex and Interactive Genetic Disorder. In Genetics and Etiology of Down Syndrome. Edited by Dey S; 2011. InTech. Galdzicki Z, Siarey R, Pearce R, Stoll J, Rapoport SI: On the cause of mental retardation in Down syndrome: extrapolation from complete and segmental trisomy 16 mouse models. Brain Res Brain Res Rev 2001, 35:11545. Pletcher MT, Wiltshire T, Cabin DE, Villanueva M, Reeves RH: Use of comparative physical and sequence mapping to annotate mouse chromosome 16 and human chromosome 21. Genomics 2001, 74:454. Davisson MT, Schmidt C, Akeson EC: Segmental trisomy of murine chromosome 16: a new model technique for studying Down syndrome. Prog Clin Biol Res 1990, 360:26380. Li Z, Yu T, Morishima M, Pao A, LaDuca J, Conroy J, Nowak N, Matsui S, Shiraishi I, Yu YE: Duplication from the complete 22.9 Mb human chromosome 21 syntenic area on mouse chromosome 16 causes cardiovascular and gastrointestinal abnormalities. Hum Mol Genet 2007, 16:1359366. Sago H, Carlson EJ, Smith DJ, Kilbridge J, Rubin EM, Mobley WC, Epstein CJ, Huang TT: Ts1Cje, a partial trisomy 16 mouse model for Down syndrome, exhibits studying and behavioral abnormalities. Proc Natl Acad Sci USA 1998, 95:6256261. Yu T, Li Z, Jia Z, Clapcote SJ, Liu C, Li S, Asrar S, Pao A, Chen R, Fan N, Carattini-Rivera S, Bechard AR, Spring S, Henkelman RM, Stoica G, Matsui S-I, Nowak NJ, Roder JC, Chen C, Bradley A, Yu YE: A mouse model of Down syndrome trisomic for all human chromosome 21 syntenic regions. Hum Mol Genet 2010, 19:2780791. Pereira PL, Magnol L, Sah I, Brault V, Duchon A, Prandini P, Gruart A, Bizot J-C, VEGFR2/KDR/Flk-1 review Chadefaux-Vekemans B, Deutsch.