{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,17]],"date-time":"2026-08-17T14:27:01Z","timestamp":1786976821630,"version":"build-2736575974"},"reference-count":20,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2013,11,21]],"date-time":"2013-11-21T00:00:00Z","timestamp":1384992000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["American J of Med Genetics Pt A"],"published-print":{"date-parts":[[2014,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:label\/>\n                    <jats:p>A recurrent proximal microdeletion at 15q25.2 with an approximate 1.5 megabase smallest region of overlap has recently been reported in seven patients and is proposed to be associated with congenital diaphragmatic hernia (CDH), mild to moderate cognitive deficit, and\/or features consistent with Diamond\u2013Blackfan anemia. We report on four further patients and define the core phenotypic features of individuals with this microdeletion to include mild to moderate developmental delay or intellectual disability, postnatal short stature, anemia, and cryptorchidism in males. CDH and structural organ malformations appear to be less frequent associations, as is venous thrombosis. There is no consistent facial dysmorphism. Features novel to our patient group include dextrocardia, obstructive sleep apnea, and cleft lip. \u00a9 2013 Wiley Periodicals, Inc.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1002\/ajmg.a.36203","type":"journal-article","created":{"date-parts":[[2013,11,21]],"date-time":"2013-11-21T16:32:43Z","timestamp":1385051563000},"page":"77-86","source":"Crossref","is-referenced-by-count":17,"title":["Characterization of core clinical phenotypes associated with recurrent proximal 15q25.2 microdeletions"],"prefix":"10.1002","volume":"164","author":[{"given":"Trent","family":"Burgess","sequence":"first","affiliation":[{"name":"Victorian Clinical Genetics Service MCRI, Royal Children's Hospital Parkville Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Natasha J.","family":"Brown","sequence":"additional","affiliation":[{"name":"Victorian Clinical Genetics Service MCRI, Royal Children's Hospital Parkville Australia"},{"name":"Department of Paediatrics Royal 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