{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,12,16]],"date-time":"2025-12-16T12:07:40Z","timestamp":1765886860752},"reference-count":26,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[2005,6,7]],"date-time":"2005-06-07T00:00:00Z","timestamp":1118102400000},"content-version":"vor","delay-in-days":3725,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Am. J. Med. Genet."],"published-print":{"date-parts":[[1995,3,27]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>We report on a family with an abnormality of 10p. The propositus has monosomy for the distal region of 10p and severe psychomotor delay, growth failure, congenital heart defect, multicystic kidney, grade V vesicoureteric reflux, and neurosensory hearing loss. The mother and the elder brother of the propositus carry a balanced reciprocal translocation (5q;10p)(q35.3;p12.3). A retarded and epileptic maternal aunt was found to have dup(10p).<\/jats:p><jats:p>Study of the family history led to the successful obstetric management of a subsequent twin pregnancy in which an affected fetus with dup(10p) was identified and selectively terminated, while the other normal twin was delivered at term without problems. \u00a9 1995 Wiley\u2010Liss, Inc.<\/jats:p>","DOI":"10.1002\/ajmg.1320560204","type":"journal-article","created":{"date-parts":[[2005,6,11]],"date-time":"2005-06-11T17:59:25Z","timestamp":1118512765000},"page":"136-140","source":"Crossref","is-referenced-by-count":13,"title":["Family with partial monosomy 10p and trisomy 10p"],"prefix":"10.1002","volume":"56","author":[{"given":"Ellis","family":"Hon","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Cyril","family":"Chapman","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Tania R.","family":"Gunn","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2005,6,7]]},"reference":[{"key":"e_1_2_1_2_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1651-2227.1977.tb07965.x"},{"key":"e_1_2_1_3_1","first-page":"61","article-title":"Monosomie partielle du bras court d'un chromosome 10: a propos d'une observation avec etude tomodensitometrique","volume":"24","author":"Bourrouillou G","year":"1981","journal-title":"Ann Genet (Paris)"},{"key":"e_1_2_1_4_1","doi-asserted-by":"publisher","DOI":"10.1136\/adc.55.6.474"},{"key":"e_1_2_1_5_1","doi-asserted-by":"publisher","DOI":"10.1001\/archpedi.1970.02100050074017"},{"key":"e_1_2_1_6_1","doi-asserted-by":"crossref","first-page":"670","DOI":"10.1542\/peds.73.5.670","article-title":"Further delineation of the 10p deletion syndrome","volume":"73","author":"Elstner CL","year":"1984","journal-title":"Pediatrics"},{"key":"e_1_2_1_7_1","first-page":"343","article-title":"Del(10)p autosomal deletion syndrome: clinical, cytogenetic and gene marker studies","volume":"26","author":"Francke U","year":"1975","journal-title":"Humangenetik"},{"key":"e_1_2_1_8_1","first-page":"189","article-title":"Distal 10p deletion syndrome","volume":"24","author":"Fryns JP","year":"1981","journal-title":"Ann Genet (Paris)"},{"key":"e_1_2_1_9_1","doi-asserted-by":"publisher","DOI":"10.1136\/jmg.20.2.107"},{"key":"e_1_2_1_10_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0022-3476(86)80124-X"},{"key":"e_1_2_1_11_1","first-page":"605","article-title":"Cytogenetic findings in a prospective series of patients with DiGeorge anomaly","volume":"43","author":"Greenberg F","year":"1988","journal-title":"Am J Hum Genet"},{"key":"e_1_2_1_12_1","first-page":"77","article-title":"Monosomie partielle du bras court d'un chromosome 10, associ\u00e9e \u00e1 un syndrome de rieger et \u00e0 un d\u00e9ficit immunitaire partiel, type DiGeorge","volume":"31","author":"Herv\u00e9 J","year":"1984","journal-title":"Ann Pediatr (Paris)"},{"key":"e_1_2_1_13_1","volume-title":"Deletion 10p Syndrome: Comparison of Findings in 3 Cases. 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