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Klopocki E, Neumann LM, T\u00f6nnies H, Ropers HH, Mundlos S, Ullmann R. Ulnar-mammary syndrome with dysmorphic facies and mental retardation caused by a novel 1.28 Mb deletion encompassing the <i>TBX3<\/i> gene. Eur J Hum Genet. 2006; 14:1274-1279.","DOI":"10.1038\/sj.ejhg.5201696"},{"key":"2","doi-asserted-by":"crossref","unstructured":"2. Koskimies E, Lindfors N, Gissler M, Peltonen J, Nietosvaara Y. Congenital upper limb deficiencies and associated malformations in Finland: A population-based study. J Hand Surg Am. 2011; 36:1058-1065.","DOI":"10.1016\/j.jhsa.2011.03.015"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3. Bamshad M, Le T, Watkins WS, <i>et al.<\/i> The spectrum of mutations in <i>TBX3<\/i>: Genotype\/Phenotype relationship in ulnar-mammary syndrome. Am J Hum Genet. 1999; 64:1550-1562.","DOI":"10.1086\/302417"},{"key":"4","doi-asserted-by":"crossref","unstructured":"4. Sasaki G, Ogata T, Ishii T, Hasegawa T, Sato S, Matsuo N. 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