{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,5,10]],"date-time":"2025-05-10T04:49:11Z","timestamp":1746852551979},"reference-count":23,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2005,6,2]],"date-time":"2005-06-02T00:00:00Z","timestamp":1117670400000},"content-version":"vor","delay-in-days":8918,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Am. J. Med. Genet."],"published-print":{"date-parts":[[1981,1]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>An Amish boy with cartilage\u2010hair hypoplasia (CHH) and cell\u2010mediated immunodeficiency developed \u201ccongenital\u201d hypoplastic anemia (CHA) of the Diamond\u2010Blackfan type by two months. Alterations of T cell function have been described separately in CHH and CHA, but this is the first known report linking the two conditions. The patient has two relatives with CHH, one with associated leukemia and one with Hodgkin disease.<\/jats:p>","DOI":"10.1002\/ajmg.1320080306","type":"journal-article","created":{"date-parts":[[2005,6,11]],"date-time":"2005-06-11T18:29:58Z","timestamp":1118514598000},"page":"291-297","source":"Crossref","is-referenced-by-count":20,"title":["Cartilage\u2010hair hypoplasia, defective T\u2010cell function, and Diamond\u2010Blackfan anemia in an Amish child"],"prefix":"10.1002","volume":"8","author":[{"given":"Richard E.","family":"Harris","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Robert L.","family":"Baehner","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sonia","family":"Gleiser","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"David D.","family":"Weaver","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M. 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