{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,25]],"date-time":"2026-09-25T05:11:18Z","timestamp":1790313078940,"version":"4.1.0"},"reference-count":15,"publisher":"Elsevier BV","issue":"2","license":[{"start":{"date-parts":[[1997,7,1]],"date-time":"1997-07-01T00:00:00Z","timestamp":867715200000},"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":[[1997,7]]},"DOI":"10.1006\/geno.1997.4793","type":"journal-article","created":{"date-parts":[[2002,10,7]],"date-time":"2002-10-07T07:11:00Z","timestamp":1033974660000},"page":"149-155","source":"Crossref","is-referenced-by-count":57,"title":["Determination of the Genomic Structure of the XNP\/ATRX Gene Encoding a Potential Zinc Finger Helicase"],"prefix":"10.1006","volume":"43","author":[{"given":"Laurent","family":"Villard","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Anne-Marie","family":"Lossi","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Carlos","family":"Cardoso","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"V.","family":"Proud","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Pierre","family":"Chiaroni","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Laurence","family":"Colleaux","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Charles","family":"Schwartz","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Michel","family":"Font\u00e9s","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1006\/geno.1997.4793_GE974793C1","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1016\/0092-8674(88)90522-3","article-title":"Zinc fingers: Guilt by association","volume":"53","author":"Evans","year":"1988","journal-title":"Cell"},{"key":"10.1006\/geno.1997.4793_GE974793C2","doi-asserted-by":"crossref","first-page":"1389","DOI":"10.1093\/hmg\/2.9.1389","article-title":"Physical and transcriptional mapping of the DXS56-PGK1 1Mb region: Identification of three new transcripts","volume":"2","author":"Gecz","year":"1993","journal-title":"Hum. Mol. Genet."},{"key":"10.1006\/geno.1997.4793_GE974793C3","doi-asserted-by":"crossref","first-page":"39","DOI":"10.1093\/hmg\/3.1.39","article-title":"Cloning and expression of the murine homologue of a putative human X-linked nuclear protein gene closely linked to PGK1 (Xq13.3)","volume":"3","author":"Gecz","year":"1994","journal-title":"Hum. Mol. Genet."},{"key":"10.1006\/geno.1997.4793_GE974793C4","doi-asserted-by":"crossref","first-page":"837","DOI":"10.1016\/0092-8674(95)90287-2","article-title":"Mutations in a putative global transcriptional regulator cause X-linked mental retardation with a-thalassemia (ATR-X syndrome)","volume":"80","author":"Gibbons","year":"1995","journal-title":"Cell"},{"key":"10.1006\/geno.1997.4793_GE974793C5","first-page":"1185","article-title":"A novel mutation in the putative DNA helicase XH2 is responsible for male-to-female sex reversal associated with an atypical form of the ATR-X syndrome","volume":"58","author":"Ion","year":"1996","journal-title":"Am. J. Hum. Genet."},{"key":"10.1006\/geno.1997.4793_GE974793C6","doi-asserted-by":"crossref","first-page":"857","DOI":"10.1093\/nar\/12.2.857","article-title":"Compilation and analysis of sequences upstream from the translational start site in eukaryotic mRNAs","volume":"12","author":"Kozak","year":"1984","journal-title":"Nucleic Acids Res."},{"key":"10.1006\/geno.1997.4793_GE974793C7","doi-asserted-by":"crossref","first-page":"41","DOI":"10.1007\/BF00210743","article-title":"The mutational spectrum of single base-pair substitutions in mRNA splice junctions of human genes: Causes and consequences","volume":"90","author":"Krawczak","year":"1992","journal-title":"Hum. Genet."},{"key":"10.1006\/geno.1997.4793_GE974793C8","doi-asserted-by":"crossref","first-page":"2887","DOI":"10.1093\/nar\/18.10.2887","article-title":"A novel, rapid method for isolation of terminal sequences from yeast artificial chromosome (YAC) clones","volume":"18","author":"Riley","year":"1990","journal-title":"Nucleic Acids Res."},{"key":"10.1006\/geno.1997.4793_GE974793C9","doi-asserted-by":"crossref","first-page":"7155","DOI":"10.1093\/nar\/15.17.7155","article-title":"RNA splice junctions of different classes of eukaryotes: Sequence statistics and functional implications in gene expression","volume":"15","author":"Shapiro","year":"1987","journal-title":"Nucleic Acids Res."},{"key":"10.1006\/geno.1997.4793_GE974793C10","doi-asserted-by":"crossref","first-page":"1957","DOI":"10.1093\/hmg\/3.11.1957","article-title":"Cloning and characterization of a new human Xq13 gene, encoding a putative helicase","volume":"3","author":"Stayton","year":"1994","journal-title":"Hum. Mol. Genet."},{"key":"10.1006\/geno.1997.4793_GE974793C11","doi-asserted-by":"crossref","first-page":"115","DOI":"10.1016\/0888-7543(95)80089-5","article-title":"Construction of a YAC contig spanning the Xq13.3 sub-band","volume":"26","author":"Villard","year":"1995","journal-title":"Genomics"},{"key":"10.1006\/geno.1997.4793_GE974793C12","first-page":"499","article-title":"Splicing mutation in the ATR-X gene can lead to a dysmorphic mental retardation phenotype without a-thalassemia","volume":"58","author":"Villard","year":"1996","journal-title":"Am. J. Hum. Genet."},{"key":"10.1006\/geno.1997.4793_GE974793C13","doi-asserted-by":"crossref","first-page":"359","DOI":"10.1038\/ng0496-359","article-title":"XNP mutation in a large family with Juberg\u2013Marsidi syndrome","volume":"12","author":"Villard","year":"1996","journal-title":"Nature Genet."},{"key":"10.1006\/geno.1997.4793_GE974793C14","doi-asserted-by":"crossref","first-page":"316","DOI":"10.1159\/000472225","article-title":"A point mutation in the XNP gene, associated with an ATR-X phenotype without pertubation in \u03b1-globin expression","volume":"4","author":"Villard","year":"1996","journal-title":"Eur. J. Hum. Genet."},{"key":"10.1006\/geno.1997.4793_GE974793C15","doi-asserted-by":"crossref","first-page":"1067","DOI":"10.1093\/nar\/18.4.1067","article-title":"A simplified protocol for fast plasmid DNA sequencing","volume":"18","author":"Zimmermann","year":"1990","journal-title":"Nucleic Acids Res."}],"container-title":["Genomics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0888754397947935?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0888754397947935?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2019,12,18]],"date-time":"2019-12-18T04:50:29Z","timestamp":1576644629000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0888754397947935"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1997,7]]},"references-count":15,"journal-issue":{"issue":"2","published-print":{"date-parts":[[1997,7]]}},"alternative-id":["S0888754397947935"],"URL":"https:\/\/doi.org\/10.1006\/geno.1997.4793","relation":{},"ISSN":["0888-7543"],"issn-type":[{"value":"0888-7543","type":"print"}],"subject":[],"published":{"date-parts":[[1997,7]]}}}