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Items: 1 to 20 of 100

1.

In search of a genetic basis for the Rett syndrome.

Martinho PS, Otto PG, Kok F, Diament A, Marques-Dias MJ, Gonzalez CH.

Hum Genet. 1990 Dec;86(2):131-4.

PMID:
2265825
2.

Cytogenetic and molecular-cytogenetic investigation of Rett syndrome: analysis of 31 cases.

Vorsanova SG, Demidova IA, Ulas VYu, Soloviev IV, Kazantzeva LZ, Yurov YuB.

Neuroreport. 1996 Dec 20;8(1):187-9.

PMID:
9051778
3.

X-inactivation in girls with Rett syndrome.

Kormann-Bortolotto MH, Woods CG, Green SH, Webb T.

Clin Genet. 1992 Dec;42(6):296-301.

PMID:
1283565
4.

[Cytogenetic and molecular genetic diagnostics of Rett syndrome in children].

Vorsanova SG, Demidova IA, Ulas VIu, Solov'ev IV, Kravets VS, Kazantseva LZ, Iurov IuB.

Zh Nevrol Psikhiatr Im S S Korsakova. 1998;98(4):53-6. Russian.

PMID:
9606901
5.

FISH analysis of replication and transcription of chromosome X loci: new approach for genetic analysis of Rett syndrome.

Vorsanova SG, Yurov YB, Kolotii AD, Soloviev IV.

Brain Dev. 2001 Dec;23 Suppl 1:S191-5.

PMID:
11738871
6.

A de novo X;3 translocation in Rett syndrome.

Zoghbi HY, Ledbetter DH, Schultz R, Percy AK, Glaze DG.

Am J Med Genet. 1990 Jan;35(1):148-51.

PMID:
2301468
7.

Is Rett syndrome a chromosome breakage syndrome?

Telvi L, Leboyer M, Chiron C, Feingold J, Ponsot G.

Am J Med Genet. 1994 Jul 15;51(4):602-5.

PMID:
7943047
8.
9.

Additional clinical and cytogenetic findings associated with Rett syndrome.

Simonic I, Gericke GS, Lippert M, Schoeman JF.

Am J Med Genet. 1997 May 31;74(3):331-7.

PMID:
9184319
10.

Alterations in replication timing of X-chromosome bands in Rett syndrome.

Kormann-Bortolotto MH, Webb T.

J Intellect Disabil Res. 1995 Apr;39 ( Pt 2):91-6.

PMID:
7787387
11.

18q-mosaicism associated with Rett syndrome phenotype.

Gordon K, Siu VM, Sergovich F, Jung J.

Am J Med Genet. 1993 Apr 15;46(2):142-4.

PMID:
8484399
12.

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.

PMID:
3087195
13.

Molecular approaches to the Rett syndrome gene.

Schanen NC.

J Child Neurol. 1999 Dec;14(12):806-14. Review.

PMID:
10614568
14.

Rett phenotype with X/autosome translocation: possible mapping to the short arm of chromosome X.

Journel H, Melki J, Turleau C, Munnich A, de Grouchy J.

Am J Med Genet. 1990 Jan;35(1):142-7.

PMID:
2301467
15.

[X chromosome inactivation patterns in patients with Rett syndrome and their mothers and the parental origin of the priority inactive X chromosome].

Jiang SL, Bao XH, Song FY, Pan H, Li MR, Wu XR.

Zhonghua Er Ke Za Zhi. 2006 Sep;44(9):648-52. Chinese.

PMID:
17217653
16.
17.

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.

PMID:
3087196
18.

Another model for the inheritance of Rett syndrome.

Bühler EM, Malik NJ, Alkan M.

Am J Med Genet. 1990 May;36(1):126-31.

PMID:
2333902
19.

Segregation of a totally skewed pattern of X chromosome inactivation in four familial cases of Rett syndrome without MECP2 mutation: implications for the disease.

Villard L, Lévy N, Xiang F, Kpebe A, Labelle V, Chevillard C, Zhang Z, Schwartz CE, Tardieu M, Chelly J, Anvret M, Fontès M.

J Med Genet. 2001 Jul;38(7):435-42.

20.

The Rett syndrome: genetics and the future.

Riccardi VM.

Am J Med Genet Suppl. 1986;1:389-402.

PMID:
3087201

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