144 related articles for article (PubMed ID: 4061771)
1. On the genetics of the Rett syndrome.
Hillig U
Brain Dev; 1985; 7(3):368-71. PubMed ID: 4061771
[TBL] [Abstract][Full Text] [Related]
2. 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.
Gillberg C; Wahlström J; Hagberg B
Brain Dev; 1985; 7(3):365-7. PubMed ID: 3864386
[TBL] [Abstract][Full Text] [Related]
3. Linkage analysis of the Rett syndrome using human chromosomal specific probes.
Anvret M; Johansson IM; Wahlström J; Hagberg B
Brain Dev; 1985; 7(3):361-4. PubMed ID: 3864385
[TBL] [Abstract][Full Text] [Related]
4. Chromosome studies in 10 patients with the Rett syndrome.
Moore JW; Tuck-Muller CM; Murphy M; Naidu S; Thomas GH
Am J Med Genet Suppl; 1986; 1():345-54. PubMed ID: 3087195
[TBL] [Abstract][Full Text] [Related]
5. Rett syndrome: lack of association with fragile site Xp22 and strategy for genetic mapping of X-linked new mutations.
Romeo G; Archidiacono N; Ferlini A; Rocchi M
Am J Med Genet Suppl; 1986; 1():355-9. PubMed ID: 3087196
[TBL] [Abstract][Full Text] [Related]
6. Chromosome findings in the Rett syndrome and a test of a two-step mutation theory.
Wahlström J; Anvret M
Am J Med Genet Suppl; 1986; 1():361-8. PubMed ID: 3087197
[TBL] [Abstract][Full Text] [Related]
7. Practical and theoretical considerations concerning the genetics of the Rett syndrome.
Wahlström J
Brain Dev; 1987; 9(5):466-8. PubMed ID: 3324796
[TBL] [Abstract][Full Text] [Related]
8. The clinical pattern of the Rett syndrome.
Hanefeld F
Brain Dev; 1985; 7(3):320-5. PubMed ID: 4061766
[TBL] [Abstract][Full Text] [Related]
9. Population genetics implications of the premutation hypothesis for the generation of the fragile X mental retardation gene.
Winter RM
Hum Genet; 1987 Mar; 75(3):269-71. PubMed ID: 3557451
[TBL] [Abstract][Full Text] [Related]
10. On the gates of hell and a most unusual gene.
Opitz JM
Am J Med Genet; 1986; 23(1-2):1-10. PubMed ID: 3953638
[No Abstract] [Full Text] [Related]
11. Gene map of mental retardation.
Wahlström J
J Ment Defic Res; 1990 Feb; 34 ( Pt 1)():11-27. PubMed ID: 2325118
[TBL] [Abstract][Full Text] [Related]
12. Fragile X syndrome: a major cause of X-linked mental retardation.
Butler MG
Compr Ther; 1988 Jul; 14(7):3-7. PubMed ID: 3060303
[No Abstract] [Full Text] [Related]
13. A variant of the fra(X) syndrome.
Bühler EM; Hadziselimovic F; Pira U
Hum Genet; 1982; 61(3):273-5. PubMed ID: 6890944
[TBL] [Abstract][Full Text] [Related]
14. A genetic diagnostic survey in an institutionalized population of 262 moderately mentally retarded patients: the Borgerstein experience.
Fryns JP; Volcke PH; Haspeslagh M; Beusen L; Van den Berghe H
J Ment Defic Res; 1990 Feb; 34 ( Pt 1)():29-40. PubMed ID: 2325119
[TBL] [Abstract][Full Text] [Related]
15. Bibliography on X-linked mental retardation, the fragile X and related subjects IV (1988).
Spano LM; Opitz JM
Am J Med Genet; 1988; 30(1-2):31-60. PubMed ID: 3052063
[No Abstract] [Full Text] [Related]
16. Linkage analysis of X-linked mental retardation with and without fragile-X using factor IX gene probe.
Choo KH; George D; Filby G; Halliday JL; Leversha M; Webb G; Danks DM
Lancet; 1984 Aug; 2(8398):349. PubMed ID: 6146889
[No Abstract] [Full Text] [Related]
17. Genetic aspects of Rett syndrome.
Zoghbi H
J Child Neurol; 1988; 3 Suppl():S76-8. PubMed ID: 3058791
[TBL] [Abstract][Full Text] [Related]
18. X linked mental retardation: a family with a separate syndrome?
Thompson EM; Gordon A; Baraitser M
J Med Genet; 1989 Jun; 26(6):373-8. PubMed ID: 2738899
[TBL] [Abstract][Full Text] [Related]
19. The genetics of Rett syndrome: the consequences of a disorder where every case is a new mutation.
Comings DE
Am J Med Genet Suppl; 1986; 1():383-8. PubMed ID: 3087200
[TBL] [Abstract][Full Text] [Related]
20. Fragile X syndrome in mildly mentally retarded children in a northern Swedish county. A prevalence study.
Blomquist HK; Gustavson KH; Holmgren G; Nordenson I; Pålsson-Stråe U
Clin Genet; 1983 Dec; 24(6):393-8. PubMed ID: 6652951
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
