{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,5]],"date-time":"2025-10-05T20:01:13Z","timestamp":1759694473522},"reference-count":25,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[2005,6,6]],"date-time":"2005-06-06T00:00:00Z","timestamp":1118016000000},"content-version":"vor","delay-in-days":4966,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Am. J. Med. Genet."],"published-print":{"date-parts":[[1991,11]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Ivemark et al. first described sibs with renal\u2010hepatic\u2010pancreatic dysplasia (RHPD) (Ivemark BI, Oldfelt V, Zetterstr\u00f6m R (1959): Acta Pediatr Scand 48:1\u201311). Subsequent reports of affected individuals have described additional malformations and syndromes associated with RHPD. In this paper we describe 2 sibs with RHPD in association with Dandy\u2010Walker cyst (DW). Through an examination of the pattern of associated malformations seen in RHPD we argue that RHPD\u2010DW is a distinct monogenetic syndrome, and not an association.<\/jats:p>","DOI":"10.1002\/ajmg.1320410214","type":"journal-article","created":{"date-parts":[[2005,6,12]],"date-time":"2005-06-12T03:45:45Z","timestamp":1118547945000},"page":"201-207","source":"Crossref","is-referenced-by-count":23,"title":["Familial renal\u2010hepatic\u2010pancreatic dysplasia and Dandy\u2010Walker cyst: A distinct syndrome?"],"prefix":"10.1002","volume":"41","author":[{"given":"A. G. W.","family":"Hunter","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C.","family":"Jimenez","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"F. G. 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