{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,24]],"date-time":"2026-07-24T15:16:35Z","timestamp":1784906195256,"version":"3.55.0"},"reference-count":18,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"2","license":[{"start":{"date-parts":[[2007,8,1]],"date-time":"2007-08-01T00:00:00Z","timestamp":1185926400000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Journal of Urology"],"published-print":{"date-parts":[[2007,8]]},"DOI":"10.1016\/j.juro.2007.04.007","type":"journal-article","created":{"date-parts":[[2007,6,16]],"date-time":"2007-06-16T10:11:17Z","timestamp":1181988677000},"page":"656-659","source":"Crossref","is-referenced-by-count":4,"title":["Genitourinary Anomalies of Pediatric FG Syndrome"],"prefix":"10.1097","volume":"178","author":[{"given":"James F.","family":"Smith","sequence":"first","affiliation":[{"name":"Division of Urology and Division of Pediatrics (Medical Genetics), Human Genetics, Pathology, Obstetrics and Gynecology, University of Utah, Salt Lake City, Utah"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Robert O.","family":"Wayment","sequence":"additional","affiliation":[{"name":"Division of Urology and Division of Pediatrics (Medical Genetics), Human Genetics, Pathology, Obstetrics and Gynecology, University of Utah, Salt Lake City, Utah"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Patrick C.","family":"Cartwright","sequence":"additional","affiliation":[{"name":"Division of Urology and Division of Pediatrics (Medical Genetics), Human Genetics, Pathology, Obstetrics and Gynecology, University of Utah, Salt Lake City, Utah"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Brent W.","family":"Snow","sequence":"additional","affiliation":[{"name":"Division of Urology and Division of Pediatrics (Medical Genetics), Human Genetics, Pathology, Obstetrics and Gynecology, University of Utah, Salt Lake City, Utah"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"John M.","family":"Opitz","sequence":"additional","affiliation":[{"name":"Division of Urology and Division of Pediatrics (Medical Genetics), Human Genetics, Pathology, Obstetrics and Gynecology, University of Utah, Salt Lake City, Utah"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","reference":[{"key":"10.1016\/j.juro.2007.04.007_bib1","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1007\/BF00439020","article-title":"Studies of malformation syndromes of man 33: the FG syndrome","volume":"117","author":"Opitz","year":"1974","journal-title":"Z Kinderheilkd"},{"key":"10.1016\/j.juro.2007.04.007_bib2","doi-asserted-by":"crossref","first-page":"297","DOI":"10.1055\/s-2004-821275","article-title":"Genetic and molecular aspects of hypospadias","volume":"14","author":"Utsch","year":"2004","journal-title":"Eur J Pediatr Surg"},{"key":"10.1016\/j.juro.2007.04.007_bib3","doi-asserted-by":"crossref","first-page":"825","DOI":"10.1002\/bdra.10084","article-title":"Molecular epidemiology of hypospadias: review of genetic and environmental risk factors","volume":"67","author":"Manson","year":"2003","journal-title":"Birth Defects Res A Clin Mol Teratol"},{"key":"10.1016\/j.juro.2007.04.007_bib4","doi-asserted-by":"crossref","first-page":"575","DOI":"10.1007\/BF03345224","article-title":"Update on cryptorchidism: endocrine, environmental and therapeutic aspects","volume":"26","author":"Brucker-Davis","year":"2003","journal-title":"J Endocrinol Invest"},{"key":"10.1016\/j.juro.2007.04.007_bib5","doi-asserted-by":"crossref","first-page":"222","DOI":"10.1002\/ajmg.a.10265","article-title":"X-linked Opitz syndrome: novel mutations in the MID1 gene and redefinition of the clinical spectrum","volume":"120","author":"De Falco","year":"2003","journal-title":"Am J Med Genet A"},{"key":"10.1016\/j.juro.2007.04.007_bib6","series-title":"FG syndrome","author":"Opitz","year":"2003"},{"key":"10.1016\/j.juro.2007.04.007_bib7","doi-asserted-by":"crossref","first-page":"83","DOI":"10.1016\/0021-9924(93)90002-R","article-title":"Language and development in FG syndrome with callosal agenesis","volume":"26","author":"McCardle","year":"1993","journal-title":"J Commun Disord"},{"key":"10.1016\/j.juro.2007.04.007_bib8","doi-asserted-by":"crossref","first-page":"139","DOI":"10.1136\/jmg.24.3.139","article-title":"FG syndrome","volume":"24","author":"Thompson","year":"1987","journal-title":"J Med Genet"},{"key":"10.1016\/j.juro.2007.04.007_bib9","first-page":"715","article-title":"The FG syndrome: perspective in 2001","volume":"27","author":"Opitz","year":"2001","journal-title":"Ital J Pediatr"},{"key":"10.1016\/j.juro.2007.04.007_bib10","doi-asserted-by":"crossref","first-page":"87","DOI":"10.1002\/(SICI)1096-8628(19971128)73:1<87::AID-AJMG17>3.0.CO;2-N","article-title":"A gene for FG syndrome maps in the Xq12-q21.31 region","volume":"73","author":"Briault","year":"1997","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.juro.2007.04.007_bib11","doi-asserted-by":"crossref","first-page":"112","DOI":"10.1002\/(SICI)1096-8628(19990910)86:2<112::AID-AJMG4>3.0.CO;2-3","article-title":"Paracentric inversion of the X chromosome [inv(X)(q12q28)] in familial FG syndrome","volume":"86","author":"Briault","year":"1999","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.juro.2007.04.007_bib12","doi-asserted-by":"crossref","first-page":"178","DOI":"10.1002\/1096-8628(20001113)95:2<178::AID-AJMG17>3.0.CO;2-V","article-title":"Mapping of X chromosome inversion breakpoints [inv(X)(q11q28)] associated with FG syndrome: a second FG locus [FGS2]?","volume":"95","author":"Briault","year":"2000","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.juro.2007.04.007_bib13","doi-asserted-by":"crossref","first-page":"6","DOI":"10.1002\/ajmg.10546","article-title":"FG syndrome: linkage analysis in two families supporting a new gene localization at Xp22.3 [FGS3]","volume":"112","author":"Dessay","year":"2002","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.juro.2007.04.007_bib14","doi-asserted-by":"crossref","first-page":"124","DOI":"10.1007\/s00439-002-0863-7","article-title":"Genetic heterogeneity of FG syndrome: a fourth locus (FGS4) maps to Xp11.4-p11.3 in an Italian family","volume":"112","author":"Piluso","year":"2003","journal-title":"Hum Genet"},{"key":"10.1016\/j.juro.2007.04.007_bib15","doi-asserted-by":"crossref","first-page":"221","DOI":"10.1002\/ajmg.a.30991","article-title":"An Xq22.3 duplication detected by comparative genomic hybridization microarray (Array-CGH) defines a new locus (FGS5) for FG syndrome","volume":"139","author":"Jehee","year":"2005","journal-title":"Am J Med Genet A"},{"key":"10.1016\/j.juro.2007.04.007_bib16","unstructured":"Piluso G: Personal communication."},{"key":"10.1016\/j.juro.2007.04.007_bib17","first-page":"695","article-title":"FGS: an unusual gene for an unusual syndrome?","volume":"27","author":"Neri","year":"2001","journal-title":"Ital J Pediatr"},{"key":"10.1016\/j.juro.2007.04.007_bib18","doi-asserted-by":"crossref","first-page":"451","DOI":"10.1038\/ng1992","article-title":"A recurrent mutation in MED12 leading to R961W causes Opitz-Kaveggia syndrome","volume":"39","author":"Risheg","year":"2007","journal-title":"Nat Genet"}],"container-title":["Journal of Urology"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/api.elsevier.com\/content\/article\/PII:S0022534707009354?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/api.elsevier.com\/content\/article\/PII:S0022534707009354?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/www.jurology.com\/doi\/pdf\/10.1016\/j.juro.2007.04.007","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,7,24]],"date-time":"2026-07-24T14:57:54Z","timestamp":1784905074000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.ovid.com\/10.1016\/j.juro.2007.04.007"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2007,8]]},"references-count":18,"journal-issue":{"issue":"2","published-print":{"date-parts":[[2007,8]]}},"alternative-id":["10.1016\/j.juro.2007.04.007"],"URL":"https:\/\/doi.org\/10.1016\/j.juro.2007.04.007","relation":{},"ISSN":["0022-5347","1527-3792"],"issn-type":[{"value":"0022-5347","type":"print"},{"value":"1527-3792","type":"electronic"}],"subject":[],"published":{"date-parts":[[2007,8]]}}}