{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,3]],"date-time":"2026-10-03T15:39:34Z","timestamp":1791041974959,"version":"4.1.0"},"reference-count":27,"publisher":"Springer Science and Business Media LLC","issue":"8","license":[{"start":{"date-parts":[[2009,8,1]],"date-time":"2009-08-01T00:00:00Z","timestamp":1249084800000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Assist Reprod Genet"],"published-print":{"date-parts":[[2009,8]]},"DOI":"10.1007\/s10815-009-9341-7","type":"journal-article","created":{"date-parts":[[2009,9,16]],"date-time":"2009-09-16T05:15:43Z","timestamp":1253078143000},"page":"461-466","source":"Crossref","is-referenced-by-count":43,"title":["Is gestation in Prader-Willi syndrome affected by the genetic subtype?"],"prefix":"10.1007","volume":"26","author":[{"given":"Merlin G.","family":"Butler","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jennifer","family":"Sturich","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Susan E.","family":"Myers","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"June-Anne","family":"Gold","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Virginia","family":"Kimonis","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Daniel J.","family":"Driscoll","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2009,9,17]]},"reference":[{"issue":"14","key":"9341_CR1","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1017\/S1462399405009531","volume":"7","author":"DC Bittel","year":"2005","unstructured":"Bittel DC, Butler MG. Prader-Willi syndrome: Clinical genetics, cytogenetics and molecular biology. Expert Rev Mol Med. 2005;7(14):1\u201320.","journal-title":"Expert Rev Mol Med."},{"key":"9341_CR2","doi-asserted-by":"crossref","first-page":"3","DOI":"10.1007\/978-0-387-33536-0_1","volume-title":"Management of Prader-Willi Syndrome","author":"MG Butler","year":"2006","unstructured":"Butler MG, Hanchett J, Thompson T. Clinical findings and natural history of Prader-Willi syndrome. In: Butler MG, Lee PDK, Whitman BY, editors. Management of Prader-Willi Syndrome. 3rd ed. Springer-Verlag Publishers: New York; 2006. p. 3\u201348.","edition":"3"},{"issue":"11","key":"9341_CR3","doi-asserted-by":"crossref","first-page":"4183","DOI":"10.1210\/jc.2008-0649","volume":"93","author":"AP Goldstone","year":"2008","unstructured":"Goldstone AP, Holland AJ, Hauffa BP, Hokken-Koelega AC, Tauber M. Recommendations for the diagnosis and management of Prader-Willi syndrome. J Clin Endocrinol Metab. 2008;93(11):4183\u201397.","journal-title":"J Clin Endocrinol Metab."},{"issue":"1","key":"9341_CR4","doi-asserted-by":"crossref","first-page":"3","DOI":"10.1038\/ejhg.2008.165","volume":"17","author":"SB Cassidy","year":"2009","unstructured":"Cassidy SB, Driscoll DJ. Prader-Willi syndrome. Eur J Hum Genet. 2009;17(1):3\u201313.","journal-title":"Eur J Hum Genet."},{"key":"9341_CR5","doi-asserted-by":"crossref","first-page":"3S","DOI":"10.1097\/00019616-200010041-00002","volume":"10","author":"MG Butler","year":"2000","unstructured":"Butler MG, Thompson T. Prader-Willi syndrome: Clinical and genetic findings. The Endocrinologist. 2000;10:3S\u201316S.","journal-title":"The Endocrinologist."},{"issue":"3 Pt 1","key":"9341_CR6","doi-asserted-by":"crossref","first-page":"565","DOI":"10.1542\/peds.113.3.565","volume":"113","author":"MG Butler","year":"2004","unstructured":"Butler MG, Bittel DC, Kibiryeva N, Talebizadeh Z, Thompson T. Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy. Pediatrics. 2004;113(3 Pt 1):565\u201373.","journal-title":"Pediatrics."},{"issue":"4","key":"9341_CR7","doi-asserted-by":"crossref","first-page":"e1276","DOI":"10.1542\/peds.2006-0424","volume":"118","author":"DC Bittel","year":"2006","unstructured":"Bittel DC, Kibiryeva N, Butler MG. Expression of 4 genes between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndrome. Pediatrics. 2006;118(4):e1276\u20131283.","journal-title":"Pediatrics."},{"issue":"1","key":"9341_CR8","doi-asserted-by":"crossref","first-page":"16","DOI":"10.1038\/ng0597-16","volume":"16","author":"T Kubota","year":"1997","unstructured":"Kubota T, Das S, Christian SL, Baylin SB, Herman JG, Ledbetter DH. Methylation-specific PCR simplifies imprinting analysis. Nat Genet. 1997;16(1):16\u20137.","journal-title":"Nat Genet."},{"issue":"12","key":"9341_CR9","doi-asserted-by":"crossref","first-page":"2001","DOI":"10.1093\/hmg\/2.12.2001","volume":"2","author":"CC Glenn","year":"1993","unstructured":"Glenn CC, Porter KA, Jong MT, Nicholls RD, Driscoll DJ. Functional imprinting and epigenetic modification of the human SNRPN gene. Hum Mol Genet. 1993;2(12):2001\u20135.","journal-title":"Hum Mol Genet."},{"key":"9341_CR10","doi-asserted-by":"crossref","first-page":"153","DOI":"10.1146\/annurev.genom.2.1.153","volume":"2","author":"RD Nicholls","year":"2001","unstructured":"Nicholls RD, Knepper JL. Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes. Annu Rev Genomics Hum Genet. 2001;2:153\u201375.","journal-title":"Annu Rev Genomics Hum Genet."},{"issue":"4","key":"9341_CR11","first-page":"701","volume":"51","author":"SB Cassidy","year":"1992","unstructured":"Cassidy SB, Lai LW, Erickson RP, Magnuson L, Thomas E, Gendron R, et al. Trisomy 15 with loss of the paternal 15 as a cause of Prader-Willi syndrome due to maternal disomy. Am J Hum Genet. 1992;51(4):701\u20138.","journal-title":"Am J Hum Genet."},{"key":"9341_CR12","first-page":"57","volume-title":"Chromosome anomalies and prenatal development: An atlas","author":"D Warburton","year":"1991","unstructured":"Warburton D, Byrne J, Canki N. Trisomy. In: Warburton D, Byrne J, Canki N, editors. Chromosome anomalies and prenatal development: An atlas. New York: Oxford University Press; 1991. p. 57\u201362."},{"issue":"4","key":"9341_CR13","doi-asserted-by":"crossref","first-page":"323","DOI":"10.1002\/(SICI)1097-0223(199604)16:4<323::AID-PD856>3.0.CO;2-5","volume":"16","author":"SL Christian","year":"1996","unstructured":"Christian SL, Smith AC, Macha M, Black SH, Elder FF, Johnson JM, et al. Prenatal diagnosis of uniparental disomy 15 following trisomy 15 mosaicism. Prenat Diagn. 1996;16(4):323\u201332.","journal-title":"Prenat Diagn."},{"issue":"9","key":"9341_CR14","doi-asserted-by":"crossref","first-page":"608","DOI":"10.1136\/jmg.29.9.608","volume":"29","author":"A Harris","year":"1992","unstructured":"Harris A, Collins J, Vetrie D, Cole C, Bobrow M. X inactivation as a mechanism of selection against lethal alleles: further investigation of incontinentia pigmenti and X linked lymphoproliferative disease. J Med Genet. 1992;29(9):608\u201314.","journal-title":"J Med Genet."},{"issue":"3","key":"9341_CR15","doi-asserted-by":"crossref","first-page":"913","DOI":"10.1086\/302552","volume":"65","author":"KK Sangha","year":"1999","unstructured":"Sangha KK, Stephenson MD, Brown CJ, Robinson WP. Extremely skewed X-chromosome inactivation is increased in women with recurrent spontaneous abortion. Am J Hum Genet. 1999;65(3):913\u20137.","journal-title":"Am J Hum Genet."},{"issue":"5","key":"9341_CR16","doi-asserted-by":"crossref","first-page":"683","DOI":"10.1002\/ana.10376","volume":"52","author":"EM Maier","year":"2002","unstructured":"Maier EM, Kammerer S, Muntau AC, Wichers M, Braun A, Roscher AA. Symptoms in carriers of adrenoleukodystrophy relate to skewed X inactivation. Ann Neurol. 2002;52(5):683\u20138.","journal-title":"Ann Neurol."},{"issue":"5","key":"9341_CR17","doi-asserted-by":"crossref","first-page":"675","DOI":"10.1007\/s10803-005-0011-z","volume":"35","author":"Z Talebizadeh","year":"2005","unstructured":"Talebizadeh Z, Bittel DC, Veatch OJ, Kibiryeva N, Butler MG. Brief report: Non-random X chromosome inactivation in females with autism. J Autism Dev Disord. 2005;35(5):675\u201381.","journal-title":"J Autism Dev Disord."},{"issue":"1\u20134","key":"9341_CR18","doi-asserted-by":"crossref","first-page":"142","DOI":"10.1159\/000014971","volume":"80","author":"BR Migeon","year":"1998","unstructured":"Migeon BR. Non-random X chromosome inactivation in mammalian cells. Cytogenet Cell Genet. 1998;80(1\u20134):142\u20138.","journal-title":"Cytogenet Cell Genet."},{"issue":"6","key":"9341_CR19","doi-asserted-by":"crossref","first-page":"1353","DOI":"10.1086\/301651","volume":"61","author":"AW Lau","year":"1997","unstructured":"Lau AW, Brown CJ, Penaherrera M, Langlois S, Kalousek DK, Robinson WP. Skewed X-chromosome inactivation is common in fetuses or newborns associated with confined placental mosaicism. Am J Hum Genet. 1997;61(6):1353\u201361.","journal-title":"Am J Hum Genet."},{"issue":"3","key":"9341_CR20","doi-asserted-by":"crossref","first-page":"319","DOI":"10.1007\/s004390050698","volume":"102","author":"AC Krepischi","year":"1998","unstructured":"Krepischi AC, Kok F, Otto PG. X chromosome-inactivation patterns in patients with Rett syndrome. Hum Genet. 1998;102(3):319\u201321.","journal-title":"Hum Genet."},{"key":"9341_CR21","doi-asserted-by":"crossref","unstructured":"Ledbetter DH, Zachary JM, Simpson JL, Golbus MS, Pergament E, Jackson L et al. Cytogenetic results from the U.S. Collaborative Study on CVS. Prenat Diagn. 1992; 12(5):317\u201345.","DOI":"10.1002\/pd.1970120503"},{"issue":"5","key":"9341_CR22","doi-asserted-by":"crossref","first-page":"469","DOI":"10.1002\/ajmg.a.31506","volume":"143","author":"MG Butler","year":"2007","unstructured":"Butler MG, Theodoro MF, Bittel DC, Kuipers PJ, Driscoll DJ, Talebizadeh Z. X-chromosome inactivation patterns in females with Prader-Willi syndrome. Am J Med Genet A. 2007;143(5):469\u201375.","journal-title":"Am J Med Genet A."},{"issue":"1","key":"9341_CR23","first-page":"74","volume":"55","author":"T Woodage","year":"1994","unstructured":"Woodage T, Prasad M, Dixon JW, Selby RE, Romain DR, Columbano-Green LM, et al. Bloom syndrome and maternal uniparental disomy for chromosome 15. Am J Hum Genet. 1994;55(1):74\u201380.","journal-title":"Am J Hum Genet."},{"key":"9341_CR24","doi-asserted-by":"crossref","unstructured":"Roback EW, Barakat AJ, Dev VG, Mbikay M, Chretien M, Butler MG. An infant with distal deletion of the long arm of chromosome 15 (q26.1-qter) and loss of insulin-like growth factor 1 receptor gene. Am J Med Genet. 1991; 38:74\u20139.","DOI":"10.1002\/ajmg.1320380117"},{"key":"9341_CR25","first-page":"30","volume":"71","author":"T Eggermann","year":"2009","unstructured":"Eggermann T. Silver-Russell and Beckwith-Wiedemann syndromes: Opposite (epi)mutations in 11p15 result in opposite clinical pictures. Horm Res. 2009;71:30\u20135.","journal-title":"Horm Res."},{"key":"9341_CR26","doi-asserted-by":"crossref","first-page":"195","DOI":"10.1016\/j.tig.2008.01.003","volume":"24","author":"T Eggermann","year":"2008","unstructured":"Eggermann T, Eggermann K, Schonherr N. Growth retardation versus overgrowth: Silver-Russell syndrome is genetically opposite to Beckwith-Wiedemann syndrome. Trends Genet. 2008;24:195\u2013204.","journal-title":"Trends Genet"},{"key":"9341_CR27","doi-asserted-by":"crossref","first-page":"611","DOI":"10.1038\/ejhg.2008.233","volume":"17","author":"J Bliek","year":"2009","unstructured":"Bliek J, Verde G, Callaway J, Maas SM, de Crescenzo A, Sparago A, et al. Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome. Eur J Hum Genet. 2009;17:611\u20139.","journal-title":"Eur J Hum Genet"}],"container-title":["Journal of Assisted Reproduction and Genetics"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s10815-009-9341-7.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/s10815-009-9341-7\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s10815-009-9341-7","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,5,31]],"date-time":"2019-05-31T01:15:51Z","timestamp":1559265351000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/s10815-009-9341-7"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2009,8]]},"references-count":27,"journal-issue":{"issue":"8","published-print":{"date-parts":[[2009,8]]}},"alternative-id":["9341"],"URL":"https:\/\/doi.org\/10.1007\/s10815-009-9341-7","relation":{},"ISSN":["1058-0468","1573-7330"],"issn-type":[{"value":"1058-0468","type":"print"},{"value":"1573-7330","type":"electronic"}],"subject":[],"published":{"date-parts":[[2009,8]]}}}