RETT SYNDROME AND FRAGILE SITE IN Xp22
Authors:
- N. ArchidiaconoNAN. Archidiacono
- A. RettARA. Rett
- M. RocchiMRM. Rocchi
- S. RolandoSRS. Rolando
- E. LugaresiELE. Lugaresi
- G. RomeoGRG. Romeo
- 1 November 1985
- journal article
- letter
- Published by Elsevier in The Lancet
- Vol. 326 (8466) , 1242-1243
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- New classes of common fragile sites induced by 5-azacytidine and bromodeoxyuridineHuman Genetics, 1985
- INFANTILE AUTISM AND RETT'S SYNDROME: COMMON CHROMOSOMAL DENOMINATORThe Lancet, 1984
- A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: Report of 35 casesAnnals of Neurology, 1983
- On the frequency of telomeric chromosomal changes induced by culture conditions suitable for fragile X expressionHuman Genetics, 1982