{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,7]],"date-time":"2026-10-07T11:06:00Z","timestamp":1791371160270,"version":"4.3.1"},"reference-count":25,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2015,9,1]],"date-time":"2015-09-01T00:00:00Z","timestamp":1441065600000},"content-version":"tdm","delay-in-days":1867,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2011,7]]},"DOI":"10.1111\/j.1399-0004.2010.01514.x","type":"journal-article","created":{"date-parts":[[2010,7,22]],"date-time":"2010-07-22T13:23:10Z","timestamp":1279804990000},"page":"83-88","source":"Crossref","is-referenced-by-count":55,"title":["Silver-Russell patients showing a broad range of ICR1 and ICR2 hypomethylation in different tissues"],"prefix":"10.1111","volume":"80","author":[{"given":"M","family":"Begemann","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"S","family":"Spengler","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"D","family":"Kanber","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"A","family":"Haake","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"M","family":"Baudis","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"I","family":"Leisten","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"G","family":"Binder","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"S","family":"Markus","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"T","family":"Rupprecht","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"H","family":"Segerer","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"S","family":"Fricke-Otto","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"R","family":"M\u00fchlenberg","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"R","family":"Siebert","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"K","family":"Buiting","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"T","family":"Eggermann","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2010,7,22]]},"reference":[{"issue":"1","key":"10.1111\/j.1399-0004.2010.01514.x-BIB1|cit1","doi-asserted-by":"crossref","first-page":"79","DOI":"10.1111\/j.1399-0004.2007.00930.x","article-title":"Use of multiplex ligation-dependent probe amplification increases the detection rate for 11p15 epigenetic alterations in Silver-Russell syndrome.","volume":"73","author":"Eggermann","year":"2008","journal-title":"Clin Genet"},{"key":"10.1111\/j.1399-0004.2010.01514.x-BIB2|cit2","doi-asserted-by":"crossref","first-page":"396","DOI":"10.1136\/jmg.2007.057059","article-title":"Mosaic maternal uniparental disomy of chromosome 11 in a patient with Silver-Russell syndrome.","volume":"45","author":"Bullman","year":"2008","journal-title":"J Med Genet"},{"key":"10.1111\/j.1399-0004.2010.01514.x-BIB3|cit3","doi-asserted-by":"crossref","first-page":"59","DOI":"10.1136\/jmg.2006.044370","article-title":"The centromeric 11p15 imprinting centre is also involved in Silver-Russell syndrome.","volume":"44","author":"Sch\u00f6nherr","year":"2007","journal-title":"J Med Genet"},{"key":"10.1111\/j.1399-0004.2010.01514.x-BIB4|cit4","doi-asserted-by":"crossref","first-page":"1025","DOI":"10.1038\/sj.ejhg.5201463","article-title":"Molecular subtypes and phenotypic expression of Beckwith-Wiedemann syndrome.","volume":"13","author":"Cooper","year":"2005","journal-title":"Eur J Hum Genet"},{"key":"10.1111\/j.1399-0004.2010.01514.x-BIB5|cit5","doi-asserted-by":"crossref","first-page":"1625","DOI":"10.1038\/ejhg.2009.77","article-title":"Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells.","volume":"17","author":"Bliek","year":"2009","journal-title":"Eur J Hum Genet"},{"key":"10.1111\/j.1399-0004.2010.01514.x-BIB6|cit6","doi-asserted-by":"crossref","first-page":"2650","DOI":"10.1093\/nar\/gki555","article-title":"ZAC, LIT1 (KCNQ1OT1) and p57KIP2 (CDKN1C) are in an imprinted gene network that may play a role in Beckwith-Wiedemann syndrome.","volume":"33","author":"Arima","year":"2005","journal-title":"Nucleic Acids Res"},{"key":"10.1111\/j.1399-0004.2010.01514.x-BIB7|cit7","doi-asserted-by":"crossref","first-page":"262","DOI":"10.1007\/s00439-006-0205-2","article-title":"A maternal hypomethylation syndrome presenting as transient neonatal diabetes mellitus.","volume":"120","author":"Mackay","year":"2006","journal-title":"Hum Genet"},{"key":"10.1111\/j.1399-0004.2010.01514.x-BIB8|cit8","doi-asserted-by":"crossref","first-page":"949","DOI":"10.1038\/ng.187","article-title":"Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57.","volume":"40","author":"Mackay","year":"2008","journal-title":"Nat Genet"},{"key":"10.1111\/j.1399-0004.2010.01514.x-BIB9|cit9","doi-asserted-by":"crossref","first-page":"902","DOI":"10.1136\/jmg.2006.042135","article-title":"The epigenetic imprinting defect of patients with Beckwith-Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region.","volume":"43","author":"Rossignol","year":"2006","journal-title":"J Med Genet"},{"key":"10.1111\/j.1399-0004.2010.01514.x-BIB10|cit10","doi-asserted-by":"crossref","first-page":"611","DOI":"10.1038\/ejhg.2008.233","article-title":"Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome.","volume":"17","author":"Bliek","year":"2009","journal-title":"Eur J Hum Genet"},{"key":"10.1111\/j.1399-0004.2010.01514.x-BIB11|cit11","doi-asserted-by":"crossref","first-page":"4724","DOI":"10.1093\/hmg\/ddp435","article-title":"Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci.","volume":"18","author":"Azzi","year":"2009","journal-title":"Hum Mol Genet"},{"key":"10.1111\/j.1399-0004.2010.01514.x-BIB12|cit12","doi-asserted-by":"crossref","first-page":"2415","DOI":"10.1002\/ajmg.a.33065","article-title":"Screening of DNA methylation at the H19 promoter or the distal region of its ICR1 ensures efficient detection of chromosome 11p15 epimutations in Russell-Silver syndrome.","volume":"149A","author":"Horike","year":"2009","journal-title":"Am J Med Genet A"},{"key":"10.1111\/j.1399-0004.2010.01514.x-BIB13|cit13","first-page":"648","article-title":"Methylation analysis of 79 patients with growth restriction reveals novel patterns of methylation change at imprinted loci.","volume":"17","author":"Turner","year":"2010","journal-title":"Eur J Med Genet"},{"key":"10.1111\/j.1399-0004.2010.01514.x-BIB14|cit14","doi-asserted-by":"crossref","first-page":"22","DOI":"10.1038\/ejhg.2008.177","article-title":"Low frequency of imprinting defects in ICSI children born small for gestational age.","volume":"17","author":"Kanber","year":"2009","journal-title":"Eur J Hum Genet"},{"key":"10.1111\/j.1399-0004.2010.01514.x-BIB15|cit15","doi-asserted-by":"crossref","first-page":"255","DOI":"10.1007\/s00439-004-1236-1","article-title":"Bisulphite sequencing of the transient neonatal diabetes mellitus DMR facilitates a novel diagnostic test but reveals no methylation anomalies in patients of unknown aetiology.","volume":"116","author":"Mackay","year":"2005","journal-title":"Hum Genet"},{"key":"10.1111\/j.1399-0004.2010.01514.x-BIB16|cit16","doi-asserted-by":"crossref","first-page":"645","DOI":"10.1002\/humu.10222","article-title":"A multiplex methylation PCR assay for identification of uniparental disomy of chromosome 7.","volume":"21","author":"Moore","year":"2003","journal-title":"Hum Mutat"},{"key":"10.1111\/j.1399-0004.2010.01514.x-BIB17|cit17","doi-asserted-by":"crossref","first-page":"e1000790.","DOI":"10.1371\/journal.pgen.1000790","article-title":"The human retinoblastoma gene is imprinted.","volume":"5","author":"Kanber","year":"2009","journal-title":"PLoS Genet"},{"key":"10.1111\/j.1399-0004.2010.01514.x-BIB18|cit18","doi-asserted-by":"crossref","first-page":"e46.","DOI":"10.1136\/jmg.40.4.e46","article-title":"Exclusion of maternal uniparental disomy of chromosome 14 in patients referred for Prader-Willi syndrome using a multiplex methylation polymerase chain reaction assay.","volume":"40","author":"Dietz","year":"2003","journal-title":"J Med Genet"},{"key":"10.1111\/j.1399-0004.2010.01514.x-BIB19|cit19","doi-asserted-by":"crossref","first-page":"637","DOI":"10.1136\/jmg.2007.050807","article-title":"Isolated imprinting mutation of the DLK1\/GTL2 locus associated with a clinical presentation of maternal uniparental disomy of chromosome 14.","volume":"44","author":"Temple","year":"2007","journal-title":"J Med Genet"},{"key":"10.1111\/j.1399-0004.2010.01514.x-BIB20|cit20","doi-asserted-by":"crossref","first-page":"3227","DOI":"10.1002\/ajmg.a.32577","article-title":"Microarray-based DNA methylation analysis of imprinted loci in a patient with transient neonatal diabetes mellitus.","volume":"146A","author":"Martin-Subero","year":"2008","journal-title":"Am J Med Genet A"},{"key":"10.1111\/j.1399-0004.2010.01514.x-BIB21|cit21","doi-asserted-by":"crossref","first-page":"2488","DOI":"10.1182\/blood-2008-04-152900","article-title":"New insights into the biology and origin of mature aggressive B-cell lymphomas by combined epigenomic, genomic, and transcriptional profiling.","volume":"113","author":"Mart\u00edn-Subero","year":"2009","journal-title":"Blood"},{"key":"10.1111\/j.1399-0004.2010.01514.x-BIB22|cit22","doi-asserted-by":"crossref","first-page":"163","DOI":"10.1038\/2464","article-title":"Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest.","volume":"20","author":"Lefebvre","year":"1998","journal-title":"Nat Genet"},{"key":"10.1111\/j.1399-0004.2010.01514.x-BIB23|cit23","doi-asserted-by":"crossref","first-page":"1317","DOI":"10.1093\/hmg\/11.11.1317","article-title":"Discordant KCNQ 1OT1 imprinting in sets of monozygotic twins discordant for Beckwith-Wiedemann syndrome.","volume":"11","author":"Weksberg","year":"2002","journal-title":"Hum Mol Genet"},{"issue":"(9385)","key":"10.1111\/j.1399-0004.2010.01514.x-BIB24|cit24","doi-asserted-by":"crossref","first-page":"735","DOI":"10.1016\/S0140-6736(03)14237-7","article-title":"Twinning.","volume":"362","author":"Hall","year":"2003","journal-title":"Lancet"},{"key":"10.1111\/j.1399-0004.2010.01514.x-BIB25|cit25","doi-asserted-by":"crossref","first-page":"444","DOI":"10.1016\/j.ejmg.2008.06.001","article-title":"Maternal uniparental disomy 7 and Silver-Russell syndrome - clinical update and comparison with other subgroups.","volume":"51","author":"Kotzot","year":"2008","journal-title":"Eur J Med Genet"}],"container-title":["Clinical Genetics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1111%2Fj.1399-0004.2010.01514.x","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/onlinelibrary.wiley.com\/wol1\/doi\/10.1111\/j.1399-0004.2010.01514.x\/fullpdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2021,7,7]],"date-time":"2021-07-07T04:29:30Z","timestamp":1625632170000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1111\/j.1399-0004.2010.01514.x"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2010,7,22]]},"references-count":25,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2011,7]]}},"URL":"https:\/\/doi.org\/10.1111\/j.1399-0004.2010.01514.x","relation":{},"ISSN":["0009-9163"],"issn-type":[{"value":"0009-9163","type":"print"}],"subject":[],"published":{"date-parts":[[2010,7,22]]}}}