Infantile autism, fragile (X) (q27.3) and RFLP analysis in an extended Swedish family.
作者信息
Anvret M, Gillberg C, Wahlström J, Albertsson-Wikland K, Davies K
机构信息
Department of Clinical Genetics, Karolinska Sjukhuset, Stockholm, Sweden.
出版信息
Clin Genet. 1988 Oct;34(4):265-71. doi: 10.1111/j.1399-0004.1988.tb02874.x.
Abstract
In an extended family with eight individuals with infantile autism, in association with other developmental disorders and fragile (X) (q27.3), DNA techniques were used to investigate linkage between X chromosomal probes and the disorder. F9 was not informative and recombination was found between fragile X and DXS15, DXS51 and DXS52.
摘要
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