Molecular characterisation of a ring chromosome 22 in a patient with severe language delay: a contribution to the refinement of the subtelomeric 22q deletion syndrome.
作者信息
De Mas P, Chassaing N, Chaix Y, Vincent M-C, Julia S, Bourrouillou G, Calvas P, Bieth E
出版信息
J Med Genet. 2002 Apr;39(4):e17. doi: 10.1136/jmg.39.4.e17.
Abstract
摘要
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