{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,25]],"date-time":"2026-04-25T08:10:06Z","timestamp":1777104606632,"version":"3.51.4"},"reference-count":15,"publisher":"Elsevier BV","issue":"5","license":[{"start":{"date-parts":[[2011,9,1]],"date-time":"2011-09-01T00:00:00Z","timestamp":1314835200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Journal de Gyn\u00e9cologie Obst\u00e9trique et Biologie de la Reproduction"],"published-print":{"date-parts":[[2011,9]]},"DOI":"10.1016\/j.jgyn.2011.01.017","type":"journal-article","created":{"date-parts":[[2011,3,9]],"date-time":"2011-03-09T12:05:04Z","timestamp":1299672304000},"page":"476-480","source":"Crossref","is-referenced-by-count":1,"title":["Un nouveau cas de diagnostic ant\u00e9natal de dysplasie frontonasale"],"prefix":"10.1016","volume":"40","author":[{"given":"V.","family":"Guigue","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A.","family":"Martin","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M.","family":"Mangin","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"F.","family":"Arbez-Gindre","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"E.","family":"Labenne","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"L.","family":"Olivier-Faivre","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"R.","family":"Ramanah","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"D.","family":"Riethmuller","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.jgyn.2011.01.017_bib0005","unstructured":"Lyons Jones K. Smith's recognizable patterns of human malformation. Kenneth Lyons Jones, 6e ed. Elsevier Saunders; 2006."},{"key":"10.1016\/j.jgyn.2011.01.017_bib0010","doi-asserted-by":"crossref","first-page":"375","DOI":"10.1002\/pd.287","article-title":"Prenatal ultrasound diagnosis of frontonasal dysplasia","volume":"22","author":"Martinelli","year":"2002","journal-title":"Prenat Diagn"},{"key":"10.1016\/j.jgyn.2011.01.017_bib0015","doi-asserted-by":"crossref","first-page":"290","DOI":"10.1046\/j.1469-0705.2002.00773.x","article-title":"Three-dimensional prenatal diagnosis of frontonasal malformation and unilateral cleft lip\/palate","volume":"20","author":"Shipp","year":"2002","journal-title":"Ultrasound Obstet Gynecol"},{"key":"10.1016\/j.jgyn.2011.01.017_bib0020","doi-asserted-by":"crossref","first-page":"187","DOI":"10.1080\/jmf.16.3.187.197","article-title":"Firt-trimester three-dimensional ultrasonographic findings in a fetus with frontonasal malformation","volume":"16","author":"Sleurs","year":"2004","journal-title":"J Matern Fetal Neonatal Med"},{"key":"10.1016\/j.jgyn.2011.01.017_bib0025","doi-asserted-by":"crossref","first-page":"1075","DOI":"10.1002\/pd.2118","article-title":"Prenatal diagnosis of frontonasal dysplasia using 3D ultrasound","volume":"28","author":"Johnstone","year":"2008","journal-title":"Prenat Diagn"},{"key":"10.1016\/j.jgyn.2011.01.017_bib0030","doi-asserted-by":"crossref","first-page":"245","DOI":"10.1097\/00019605-199707000-00008","article-title":"Fronto-facio-nasal dysplasia","volume":"6","author":"Suthers","year":"1997","journal-title":"Clin Dysmorphol"},{"key":"10.1016\/j.jgyn.2011.01.017_bib0035","doi-asserted-by":"crossref","first-page":"34","DOI":"10.7150\/ijms.1.34","article-title":"The syndrome of frontonasal dysplasia, callosal agenesis, basal encephalocele, and eye anomalies-phenotypic an aetiological considerations","volume":"1","author":"Richieiri-Costa","year":"2004","journal-title":"Int J Med Sci"},{"key":"10.1016\/j.jgyn.2011.01.017_bib0040","doi-asserted-by":"crossref","first-page":"107","DOI":"10.1136\/jmg.24.2.107","article-title":"Frontonasal dysplasia associated with tetralogy of Fallot","volume":"24","author":"De Moor","year":"1987","journal-title":"J Med Genet"},{"key":"10.1016\/j.jgyn.2011.01.017_bib0045","doi-asserted-by":"crossref","first-page":"1145","DOI":"10.1111\/j.1651-2227.2000.tb03368.x","article-title":"Fronto-facio-nasal dysplasia in two sisters with additional findings","volume":"89","author":"Ozkinay","year":"2000","journal-title":"Acta Paediatr"},{"key":"10.1016\/j.jgyn.2011.01.017_bib0050","doi-asserted-by":"crossref","first-page":"698","DOI":"10.1016\/j.ajhg.2009.04.009","article-title":"Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3\u00a0homeobox gene","volume":"84","author":"Twigg","year":"2009","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.jgyn.2011.01.017_bib0055","doi-asserted-by":"crossref","first-page":"51","DOI":"10.1016\/S0165-5876(00)00341-4","article-title":"The syndrome of frontonasal dysplasia, spastic paraplegia, mental retardation and blindness: a case report with CT scan findings and review of literature","volume":"54","author":"Dubey","year":"2000","journal-title":"Int J Pediatr Otorhinolaryngol"},{"key":"10.1016\/j.jgyn.2011.01.017_bib0060","doi-asserted-by":"crossref","first-page":"4357","DOI":"10.1093\/hmg\/ddp391","article-title":"ALX4\u00a0dysfunction disrupts craniofacial and epidermal development","volume":"18","author":"Kayserili","year":"2009","journal-title":"Hum Mol Genet"},{"key":"10.1016\/j.jgyn.2011.01.017_bib0065","first-page":"63","article-title":"Frontonasal dysplasia: a family presenting autosomal dominant inheritance pattern","volume":"20","author":"Kocak","year":"2009","journal-title":"Genet Counsel"},{"key":"10.1016\/j.jgyn.2011.01.017_bib0070","doi-asserted-by":"crossref","first-page":"110","DOI":"10.1016\/j.ymgme.2005.07.017","article-title":"Clinical and genetic aspects of craniofrontonasal syndrome: towards resolving a genetic paradox","volume":"86","author":"Wieacker","year":"2005","journal-title":"Mol Genet Metab"},{"key":"10.1016\/j.jgyn.2011.01.017_bib0075","doi-asserted-by":"crossref","first-page":"67","DOI":"10.1159\/000134826","article-title":"P450\u00a0oxidoreductase deficiency-a new form of congenital adrenal hyperplasia","volume":"13","author":"Fluck","year":"2008","journal-title":"Endoc Dev"}],"container-title":["Journal de Gyn\u00e9cologie Obst\u00e9trique et Biologie de la Reproduction"],"original-title":[],"language":"fr","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S036823151100041X?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S036823151100041X?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2018,12,3]],"date-time":"2018-12-03T22:22:13Z","timestamp":1543875733000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S036823151100041X"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2011,9]]},"references-count":15,"journal-issue":{"issue":"5","published-print":{"date-parts":[[2011,9]]}},"alternative-id":["S036823151100041X"],"URL":"https:\/\/doi.org\/10.1016\/j.jgyn.2011.01.017","relation":{},"ISSN":["0368-2315"],"issn-type":[{"value":"0368-2315","type":"print"}],"subject":[],"published":{"date-parts":[[2011,9]]}}}