{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,3]],"date-time":"2025-11-03T09:00:12Z","timestamp":1762160412255},"reference-count":21,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2005,6,3]],"date-time":"2005-06-03T00:00:00Z","timestamp":1117756800000},"content-version":"vor","delay-in-days":6028,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Am. J. Med. Genet."],"published-print":{"date-parts":[[1988,12]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Greig cephalopolysyndactyly syndrome is an autosomal dominant form of complex polydactyly in man. Attention is called to the evidence that, on both morphological and comparative gene mapping grounds, this defect is homologous to <jats:italic>Xt<\/jats:italic>\u2010extra toes in the mouse. The pattern of polydactyly in both species is very similar. In addition, both conditions probably map close to the T\u2010cell receptor gamma polypeptide at 13 A2\u20133 in mouse and 7p15 in humans.<\/jats:p>","DOI":"10.1002\/ajmg.1320310411","type":"journal-article","created":{"date-parts":[[2005,6,12]],"date-time":"2005-06-12T00:53:04Z","timestamp":1118537584000},"page":"793-798","source":"Crossref","is-referenced-by-count":40,"title":["Greig cephalopolysyndactyly syndrome: A possible mouse homologue (<i>Xt<\/i>\u2010extra toes)"],"prefix":"10.1002","volume":"31","author":[{"given":"Robin M.","family":"Winter","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Susan M.","family":"Huson","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"David J.","family":"Prieur","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"James F.","family":"Reynolds","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2005,6,3]]},"reference":[{"key":"e_1_2_1_2_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1399-0004.1983.tb00080.x"},{"key":"e_1_2_1_3_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320130307"},{"key":"e_1_2_1_4_1","first-page":"818","article-title":"Greig cephalopolysyndactyly syndrome","volume":"133","author":"Duncan PA","year":"1979","journal-title":"Am J Dis Child"},{"key":"e_1_2_1_5_1","doi-asserted-by":"publisher","DOI":"10.1007\/BF00477055"},{"key":"e_1_2_1_6_1","doi-asserted-by":"publisher","DOI":"10.1007\/BF00441928"},{"key":"e_1_2_1_7_1","first-page":"299","article-title":"Syndrome dominant associant polysyndactylie, pouces en spatule, anomalies faciales et retard mental (une forme particuliere de l'acrocephalopolysyndactylie de type Noack)","volume":"19","author":"Gnamey D","year":"1971","journal-title":"J Genet Hum"},{"key":"e_1_2_1_8_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320220106"},{"key":"e_1_2_1_9_1","first-page":"189","article-title":"Oxycephaly","volume":"33","author":"Greig DM","year":"1926","journal-title":"Edinburgh Med J"},{"key":"e_1_2_1_10_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1399-0004.1972.tb01734.x"},{"key":"e_1_2_1_11_1","first-page":"543","article-title":"Extra\u2010toes: A new mutant gene causing multiple abnormalities in the mouse","volume":"17","author":"Johnson DR","year":"1967","journal-title":"J Embryol Exp Morphol"},{"key":"e_1_2_1_12_1","doi-asserted-by":"publisher","DOI":"10.1017\/S0016672300002962"},{"key":"e_1_2_1_13_1","doi-asserted-by":"publisher","DOI":"10.1126\/science.3918347"},{"key":"e_1_2_1_14_1","first-page":"489","article-title":"Greig cephalopolysyndactyly syndrome: Report of a sporadic case","volume":"40","author":"Kunze J","year":"1985","journal-title":"Helv Paediatr Acta"},{"key":"e_1_2_1_15_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1399-0004.1983.tb02240.x"},{"key":"e_1_2_1_16_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0022-3476(70)80058-0"},{"key":"e_1_2_1_17_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1651-2227.1981.tb05557.x"},{"key":"e_1_2_1_18_1","doi-asserted-by":"publisher","DOI":"10.1038\/316549a0"},{"key":"e_1_2_1_19_1","first-page":"381","article-title":"The Greig cephalopolysyndactyly syndrome","volume":"41","author":"Pelz L","year":"1986","journal-title":"Helv Paediatr Acta"},{"key":"e_1_2_1_20_1","doi-asserted-by":"publisher","DOI":"10.1016\/0888-7543(87)90099-1"},{"key":"e_1_2_1_21_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320160304"},{"key":"e_1_2_1_22_1","doi-asserted-by":"crossref","unstructured":"WinterRM(1988):Malformation syndromes: A review of mouse\/human homology. 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