Chromosomal breakage, endomitosis, endoreduplication, and hypersensitivity toward radiomimetric and alkylating agents: a possible new autosomal recessive mutation in a girl with craniosynostosis and microcephaly. [electronic resource]
Producer: 19931221Description: 339-46 p. digitalISSN:- 0340-6717
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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