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Abnormalities of the myelopoietic series indicate that it might be a stem cell disease and the presence of skeletal anomalies of the hands suggests a genetic relationship to some cases of Fanconi and Diamond anaemia. No serum lipid or vitamin E deficiency was present as in type II congenital dyserythropoietic anaemia. Serial serum ferritin determinations incidated that iron stores are increased early in type I congenital dyserythropoietic anaemia despite no transfusion load.<\/jats:p>","DOI":"10.1111\/j.1600-0609.1978.tb02496.x","type":"journal-article","created":{"date-parts":[[2010,8,4]],"date-time":"2010-08-04T18:16:22Z","timestamp":1280945782000},"page":"72-79","source":"Crossref","is-referenced-by-count":18,"title":["Type I Congenital Dyserythropoietic Anaemia with Myelopoietic Abnormalities and Hand Malformations"],"prefix":"10.1111","volume":"21","author":[{"given":"L.","family":"Holmberg","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"L.","family":"Jansson","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A.","family":"Rausing","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"P.","family":"Henriksson","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2009,4,24]]},"reference":[{"key":"e_1_2_1_2_1","doi-asserted-by":"publisher","DOI":"10.1136\/jcp.25.4.326"},{"key":"e_1_2_1_3_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1365-2141.1977.tb00577.x"},{"key":"e_1_2_1_4_1","doi-asserted-by":"publisher","DOI":"10.1182\/blood.V19.3.296.296"},{"key":"e_1_2_1_5_1","first-page":"155","article-title":"Letter to the Editor","volume":"43","author":"Bethlenfalvay N C","year":"1974","journal-title":"Blood"},{"key":"e_1_2_1_6_1","doi-asserted-by":"publisher","DOI":"10.1001\/archinte.134.2.346"},{"key":"e_1_2_1_7_1","first-page":"653","article-title":"Dys\u00e9rythropoi\u00e8se cong\u00e9nitale (Etude de 6 observations)","volume":"12","author":"Clauvel J P","year":"1972","journal-title":"Now Rev Fran\u00e7 d'H\u00e9matol"},{"key":"e_1_2_1_8_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1365-2141.1969.tb05660.x"},{"key":"e_1_2_1_9_1","first-page":"225","volume-title":"Practical haematology","author":"Dacie J V","year":"1968"},{"key":"e_1_2_1_10_1","first-page":"166","volume-title":"Congenital Disorders of Erythropoiesis","author":"Frisch B","year":"1976"},{"key":"e_1_2_1_11_1","first-page":"669","article-title":"Studies of tocopherol deficiency in infants and children. 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