{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,14]],"date-time":"2026-04-14T00:46:36Z","timestamp":1776127596876,"version":"3.50.1"},"reference-count":26,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2005,6,5]],"date-time":"2005-06-05T00:00:00Z","timestamp":1117929600000},"content-version":"vor","delay-in-days":5634,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Am. J. Med. Genet."],"published-print":{"date-parts":[[1990,1]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Two brothers of normal first\u2010cousin parents were found to have Robinow syndrome. Their paternal uncle also married a first cousin and had 3 similarly affected children (2 boys, 1 girl). The 2 affected brothers had short stature, mesomelic and acromelic brachymelia, characteristic face with hypertelorism, wide palpebral fissures, midface hypoplasia and large mouth, and hypogenitalism. Parental consanguinity and affected individuals in 2 sibships of common ancestry strongly suggest autosomal recessive inheritance. Similar cases from the literature are briefly reviewed.<\/jats:p>","DOI":"10.1002\/ajmg.1320350112","type":"journal-article","created":{"date-parts":[[2005,6,12]],"date-time":"2005-06-12T03:34:51Z","timestamp":1118547291000},"page":"64-68","source":"Crossref","is-referenced-by-count":41,"title":["Autosomal recessive Robinow syndrome"],"prefix":"10.1002","volume":"35","author":[{"given":"Ahmad S.","family":"Teebi","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2005,6,5]]},"reference":[{"key":"e_1_2_1_2_1","doi-asserted-by":"publisher","DOI":"10.1136\/jmg.23.4.350"},{"key":"e_1_2_1_3_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1399-0004.1987.tb02773.x"},{"key":"e_1_2_1_4_1","first-page":"351","article-title":"Picture of the month: Fetal face syndrome (Robinow syndrome)","volume":"129","author":"Gellis SS","year":"1975","journal-title":"Am J Dis Child"},{"key":"e_1_2_1_5_1","first-page":"409","article-title":"A radiological diagnosis of fetal face (Robinow) syndrome (mesomelic dwarfism and small genitalia)","volume":"30","author":"Giedion A","year":"1975","journal-title":"Helv Paediatr Acta"},{"key":"e_1_2_1_6_1","first-page":"2774","article-title":"Report on a variant of the fetal face syndrome with acral dysostosis","volume":"187","author":"Hanssler H","year":"1975","journal-title":"Klin Padiatr"},{"key":"e_1_2_1_7_1","doi-asserted-by":"publisher","DOI":"10.1001\/archpedi.1975.02120400081022"},{"key":"e_1_2_1_8_1","first-page":"327","article-title":"Robinow's syndrome","volume":"40","author":"Khayat D","year":"1983","journal-title":"Arch Fr Pediatr"},{"key":"e_1_2_1_9_1","first-page":"47","article-title":"The fetal face syndrome or Robinow syndrome. 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