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A “new” chromosome marker common to the Rett syndrome and infantile autism? the frequency of fragile sites at X P22 in 81 children with infantile autism, childhood psychosis and the Rett syndrome

✍ Scribed by Gillberg, Christopher; Wahlström, Jan; Hagberg, Bengt


Book ID
122090072
Publisher
Elsevier Science
Year
1985
Tongue
English
Weight
268 KB
Volume
7
Category
Article
ISSN
0387-7604

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