{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,4]],"date-time":"2026-10-04T05:33:19Z","timestamp":1791091999026,"version":"4.1.0"},"reference-count":18,"publisher":"Elsevier BV","issue":"3","license":[{"start":{"date-parts":[[1997,8,1]],"date-time":"1997-08-01T00:00:00Z","timestamp":870393600000},"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":["Genomics"],"published-print":{"date-parts":[[1997,8]]},"DOI":"10.1006\/geno.1997.4837","type":"journal-article","created":{"date-parts":[[2002,10,7]],"date-time":"2002-10-07T11:11:00Z","timestamp":1033989060000},"page":"390-394","source":"Crossref","is-referenced-by-count":32,"title":["Genomic Organization of the Faciogenital Dysplasia (FGD1; Aarskog Syndrome) Gene"],"prefix":"10.1006","volume":"43","author":[{"given":"N.German","family":"Pasteris","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Joshua","family":"Buckler","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Amy B.","family":"Cadle","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jerome L.","family":"Gorski","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1006\/geno.1997.4837_GE974837C1","doi-asserted-by":"crossref","first-page":"856","DOI":"10.1016\/S0022-3476(70)80247-5","article-title":"A familial syndrome of short stature associated with facial dysplasia and genital anomalies","volume":"77","author":"Aarskog","year":"1970","journal-title":"J. Pediatr."},{"key":"10.1006\/geno.1997.4837_GE974837C2","doi-asserted-by":"crossref","first-page":"216","DOI":"10.1016\/S0955-0674(96)80068-8","article-title":"The Dbl family of oncogenes","volume":"8","author":"Cerione","year":"1996","journal-title":"Curr. Opin. Cell Biol."},{"key":"10.1006\/geno.1997.4837_GE974837C3","doi-asserted-by":"crossref","first-page":"5695","DOI":"10.1073\/pnas.91.12.5695","article-title":"Effective amplification of long targets from cloned inserts and human genomic DNA","volume":"91","author":"Cheng","year":"1994","journal-title":"Proc. Natl. Acad. Sci. USA"},{"key":"10.1006\/geno.1997.4837_GE974837C4","doi-asserted-by":"crossref","first-page":"420","DOI":"10.1002\/ajmg.1320430164","article-title":"Aarskog syndrome: The changing phenotype with age","volume":"43","author":"Fryns","year":"1992","journal-title":"Am. J. Med. Genet."},{"key":"10.1006\/geno.1997.4837_GE974837C5","series-title":"Syndromes of the Head and Neck","author":"Gorlin","year":"1990"},{"key":"10.1006\/geno.1997.4837_GE974837C6","series-title":"Textbook of Molecular Medicine","article-title":"Aarskog\u2013Scott syndrome","author":"Gorski","year":"1997"},{"key":"10.1006\/geno.1997.4837_GE974837C7","doi-asserted-by":"crossref","first-page":"39","DOI":"10.1002\/ajmg.1320150105","article-title":"Autosomal dominant inheritance of the Aarskog syndrome","volume":"15","author":"Grier","year":"1983","journal-title":"Am. J. Med. Genet."},{"key":"10.1006\/geno.1997.4837_GE974837C8","first-page":"3123","article-title":"Characterization of the transcriptional regulatory region of the human WT1 gene","volume":"8","author":"Hofmann","year":"1993","journal-title":"Oncogene"},{"key":"10.1006\/geno.1997.4837_GE974837C9","doi-asserted-by":"crossref","first-page":"16","DOI":"10.1016\/0168-9525(94)90014-0","article-title":"What do BMPs do in mammal? Clues from the mouse short-ear mutation","volume":"10","author":"Kingsley","year":"1994","journal-title":"Trends Genet."},{"key":"10.1006\/geno.1997.4837_GE974837C10","doi-asserted-by":"crossref","first-page":"1237","DOI":"10.1126\/science.3296191","article-title":"Regulation of inducible and tissue-specific gene expression","volume":"236","author":"Maniatis","year":"1987","journal-title":"Science"},{"key":"10.1006\/geno.1997.4837_GE974837C11","doi-asserted-by":"crossref","first-page":"247","DOI":"10.1016\/0022-2836(87)90647-4","article-title":"Signals for the selection of a splice site in pre-mRNA: Computer analysis of splice junction sequences and like sequences","volume":"195","author":"Ohshima","year":"1987","journal-title":"J. Mol. Biol."},{"key":"10.1006\/geno.1997.4837_GE974837C12","doi-asserted-by":"crossref","first-page":"1628","DOI":"10.1016\/S0960-9822(02)70786-0","article-title":"Faciogenital dysplasia protein (FGD1) and Vav, two related proteins required for normal embryonic development, are upstream regulators of Rho GTPases","volume":"6","author":"Olsen","year":"1996","journal-title":"Curr. Biol."},{"key":"10.1006\/geno.1997.4837_GE974837C13","doi-asserted-by":"crossref","first-page":"5275","DOI":"10.1093\/nar\/21.22.5275","article-title":"YAC subclone contig assembly by serial interspersed repetitive sequence (IRS)\u2013PCR product hybridizations","volume":"21","author":"Pasteris","year":"1993","journal-title":"Nucleic Acids Res."},{"key":"10.1006\/geno.1997.4837_GE974837C14","doi-asserted-by":"crossref","first-page":"669","DOI":"10.1016\/0092-8674(94)90552-5","article-title":"Isolation and characterization of the faciogenital dysplasia (Aarskog\u2013Scott syndrome) gene: A putative Rho\/Rac guanine nucleotide exchange factor","volume":"79","author":"Pasteris","year":"1994","journal-title":"Cell"},{"key":"10.1006\/geno.1997.4837_GE974837C15","doi-asserted-by":"crossref","first-page":"298","DOI":"10.1016\/S0888-7543(05)80219-8","article-title":"The gene for Aarskog syndrome is located between DXS255 and DXS566 (Xp11.2\u2013Xq13)","volume":"14","author":"Porteous","year":"1994","journal-title":"Genomics"},{"key":"10.1006\/geno.1997.4837_GE974837C16","series-title":"Molecular Cloning: A Laboratory Manual","author":"Sambrook","year":"1989"},{"key":"10.1006\/geno.1997.4837_GE974837C17","first-page":"595","article-title":"Aarskog-Scott syndrome: Confirmation of linkage to the pericentric region of the X chromosome","volume":"17","author":"Stevenson","year":"1994","journal-title":"Am. J. Med. Genet."},{"key":"10.1006\/geno.1997.4837_GE974837C18","doi-asserted-by":"crossref","first-page":"33169","DOI":"10.1074\/jbc.271.52.33169","article-title":"The faciogenital dysplasia gene product FGD1 functions as a Cdc42Hs-specific guanine-nucleotide exchange factor","volume":"271","author":"Zheng","year":"1996","journal-title":"J. Biol. Chem."}],"container-title":["Genomics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0888754397948370?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0888754397948370?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2019,5,6]],"date-time":"2019-05-06T19:50:07Z","timestamp":1557172207000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0888754397948370"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1997,8]]},"references-count":18,"journal-issue":{"issue":"3","published-print":{"date-parts":[[1997,8]]}},"alternative-id":["S0888754397948370"],"URL":"https:\/\/doi.org\/10.1006\/geno.1997.4837","relation":{},"ISSN":["0888-7543"],"issn-type":[{"value":"0888-7543","type":"print"}],"subject":[],"published":{"date-parts":[[1997,8]]}}}