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In the son a high frequency of chromosome breaks in lymphocytes was found.<\/jats:p><jats:p>We compare this familial syndrome to Fanconi anemia and other radial ray aplasia syndromes and conclude that we are dealing with a different entity, which apparently is inherited as a dominant trait.<\/jats:p>","DOI":"10.1002\/ajmg.1320140121","type":"journal-article","created":{"date-parts":[[2005,6,11]],"date-time":"2005-06-11T15:34:20Z","timestamp":1118504060000},"page":"151-157","source":"Crossref","is-referenced-by-count":18,"title":["Radial ray aplasia and renal anomalies in father and son: A new syndrome"],"prefix":"10.1002","volume":"14","author":[{"given":"Shaul","family":"Sofer","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jacob","family":"Bar\u2010Ziv","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Dvorah","family":"Abeliovich","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2005,6,3]]},"reference":[{"key":"e_1_2_1_2_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320060105"},{"key":"e_1_2_1_3_1","doi-asserted-by":"crossref","first-page":"128","DOI":"10.1542\/peds.67.1.128","article-title":"Prenatal and postnatal diagnosis and carrier detection of Fanconi anemia by a clastogenic method","volume":"67","author":"Auerbach AD","year":"1981","journal-title":"Pediatrics"},{"key":"e_1_2_1_4_1","volume-title":"Congenital deformities of the upper extremities. 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