Video Upload Options

References

1. Bonaglia MC, Marelli S, Novara F, Commodaro S, Borgatti R, Minardo G, Memo L, Mangold E, Beri S, Zucca C, Brambilla D, Molteni M, Giorda R, Weber RG, Zuffardi O. Genotype-phenotype relationship in three cases with overlapping 19p13.12microdeletions. Eur J Hum Genet. 2010 Dec;18(12):1302-9. doi:10.1038/ejhg.2010.115.
2. Dolan M, Mendelsohn NJ, Pierpont ME, Schimmenti LA, Berry SA, Hirsch B. Anovel microdeletion/microduplication syndrome of 19p13.13. Genet Med. 2010Aug;12(8):503-11. doi: 10.1097/GIM.0b013e3181e59291.
3. Gilbert F. Disease genes and chromosomes: disease maps of the human genome.Chromosome 19. Genet Test. 1997;1(2):145-9.
4. Grimwood J, Gordon LA, Olsen A, Terry A, Schmutz J, Lamerdin J, Hellsten U,Goodstein D, Couronne O, Tran-Gyamfi M, Aerts A, Altherr M, Ashworth L, BajorekE, Black S, Branscomb E, Caenepeel S, Carrano A, Caoile C, Chan YM, ChristensenM, Cleland CA, Copeland A, Dalin E, Dehal P, Denys M, Detter JC, Escobar J,Flowers D, Fotopulos D, Garcia C, Georgescu AM, Glavina T, Gomez M, Gonzales E,Groza M, Hammon N, Hawkins T, Haydu L, Ho I, Huang W, Israni S, Jett J, Kadner K,Kimball H, Kobayashi A, Larionov V, Leem SH, Lopez F, Lou Y, Lowry S, Malfatti S,Martinez D, McCready P, Medina C, Morgan J, Nelson K, Nolan M, Ovcharenko I,Pitluck S, Pollard M, Popkie AP, Predki P, Quan G, Ramirez L, Rash S, Retterer J,Rodriguez A, Rogers S, Salamov A, Salazar A, She X, Smith D, Slezak T, SolovyevV, Thayer N, Tice H, Tsai M, Ustaszewska A, Vo N, Wagner M, Wheeler J, Wu K, Xie G, Yang J, Dubchak I, Furey TS, DeJong P, Dickson M, Gordon D, Eichler EE,Pennacchio LA, Richardson P, Stubbs L, Rokhsar DS, Myers RM, Rubin EM, Lucas SM. The DNA sequence and biology of human chromosome 19. Nature. 2004 Apr1;428(6982):529-35.
5. Nilsson CL, Berven F, Selheim F, Liu H, Moskal JR, Kroes RA, Sulman EP, ConradCA, Lang FF, Andrén PE, Nilsson A, Carlsohn E, Lilja H, Malm J, Fenyö D,Subramaniyam D, Wang X, Gonzales-Gonzales M, Dasilva N, Diez P, Fuentes M,Végvári Á, Sjödin K, Welinder C, Laurell T, Fehniger TE, Lindberg H, Rezeli M,Edula G, Hober S, Marko-Varga G. Chromosome 19 annotations with diseasespeciation: a first report from the Global Research Consortium. J Proteome Res.2013 Jan 4;12(1):135-50. doi: 10.1021/pr3008607.