TY - JOUR
AU - Wagstaff, J
AB - GENOMIC IMPRINTING AND DISORDERS 361 Okuizumi H, Muramatsu M, Komatsubara H, Shiroishi T, Moriwaki K, Katsuki M, Hatano N, Sasaki, H, Ueda T, Mise N, Takagi N, Plass C, Chapman VM (1994): Identification of an imprinted U2af binding protein related sequence on mouse chromosome 1l using the RLGS method. Nature Genet 6:33-40 Jinno Y, Yun K, Nishiwaki K, Kubota T, Ogawa O, Reeve AE, Niikawa N (1994): Mosaic and polymorphic imprinting of the WT1 gene in humans. Nature Genet 6:305-309 Jinno Y, Ikeda Y, Yun K, Maw M, Masuzaki H, Fukuda H, Inuzuka K, Fujishita A, Ohtani Y, Okimoto T, Ishimaru T, Niikawa N (1995): Establishment of functional imprinting of the HI9 gene in human developing placentae. Nature Genet 10:318-324 Kajii T, Ohama K (1977): Androgenetic origin of hydatidiform mole. Nature 268:633-634 Kaneko-Ishino T, Kuroiwa Y, Miyoshi N, Kohda T, Suzuki R, Yokoyama M, Viville S, Barton SC, Ishino F, Surani MA (1995): Pegl/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization. Nature Genet 11:52-59 Kotzot D, Schmitt S, Bernasconi F, Robinson WP, Lurie IW, Ilyina H, Mehes K, Hamel BCJ, Otten BJ, Hergersberg M, Werder E, Schoenle E, Schinzel A (1995): Uniparental disomy 7 in Silver-Russell 
TI - UBE3A/E6-AP mutations cause Angelman syndrome
JF - Journal of Human Genetics
DO - 10.1007/BF01876326
DA - 2005-06-08
UR - https://www.deepdyve.com/lp/springer-journals/ube3a-e6-ap-mutations-cause-angelman-syndrome-8ubgPBAMj0
SP - 361
EP - 361
VL - 41
IS - 4
DP - DeepDyve
ER -