These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

127 related articles for article (PubMed ID: 3087201)

  • 1. The Rett syndrome: genetics and the future.
    Riccardi VM
    Am J Med Genet Suppl; 1986; 1():389-402. PubMed ID: 3087201
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. Rett syndrome--search for genetic markers.
    Hanefeld F; Hanefeld U; Wilichowski E; Schmidtke J
    Am J Med Genet Suppl; 1986; 1():377-82. PubMed ID: 3087199
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. On the genetics of Rett syndrome: analysis of family and pedigree data.
    Killian W
    Am J Med Genet Suppl; 1986; 1():369-76. PubMed ID: 3087198
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Unusual X chromosome inactivation in a mentally retarded girl with an interstitial deletion Xq27: implications for the fragile X syndrome.
    Schmidt M; Certoma A; Du Sart D; Kalitsis P; Leversha M; Fowler K; Sheffield L; Jack I; Danks DM
    Hum Genet; 1990 Mar; 84(4):347-52. PubMed ID: 2307456
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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. PubMed ID: 11738871
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Earlier finishing of Xp21.2 subband replication of the inactive X chromosome in Rett syndrome girl but not in her 47,XXX mother.
    Panasiuk B; Midro AT; Zadrozna-Tołwińska B
    Clin Genet; 1997 Aug; 52(2):120-5. PubMed ID: 9298748
    [TBL] [Abstract][Full Text] [Related]  

  • 11. X-inactivation in girls with Rett syndrome.
    Kormann-Bortolotto MH; Woods CG; Green SH; Webb T
    Clin Genet; 1992 Dec; 42(6):296-301. PubMed ID: 1283565
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. The inactivation of the fragile X chromosome in female carriers of the Martin Bell syndrome as studied by two different methods.
    Tuckerman E; Webb T
    Clin Genet; 1989 Jul; 36(1):25-30. PubMed ID: 2766560
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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. PubMed ID: 2265825
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Functional mosaic trisomy of 1q12-->1q21 resulting from X-autosome insertion translocation with random inactivation.
    Vust A; Riordan D; Wickstrom D; Chudley AE; Dawson AJ
    Clin Genet; 1998 Jul; 54(1):70-3. PubMed ID: 9727744
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Heterochromatinization of human X-chromosomes: classification of replication profile.
    Babu A; Chemitiganti S; Verma RS
    Clin Genet; 1986 Aug; 30(2):108-11. PubMed ID: 3757299
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical recognition of Rett syndrome.
    Philippart M
    Am J Med Genet Suppl; 1986; 1():111-8. PubMed ID: 3087171
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Coffin-Lowry phenotype in a patient with a complex chromosome rearrangement.
    Concannon N; Hegarty AM; Stallings RL; Reardon W
    J Med Genet; 2002 Aug; 39(8):e41. PubMed ID: 12161608
    [No Abstract]   [Full Text] [Related]  

  • 19. A 5-megabase familial deletion removes the IDS and FMR-1 genes in a male Hunter patient.
    Birot AM; Delobel B; Gronnier P; Bonnet V; Maire I; Bozon D
    Hum Mutat; 1996; 7(3):266-8. PubMed ID: 8829661
    [No Abstract]   [Full Text] [Related]  

  • 20. A new syndrome with mental retardation, short stature and an Xq duplication.
    Thode A; Partington MW; Yip MY; Chapman C; Richardson VF; Turner G
    Am J Med Genet; 1988; 30(1-2):239-50. PubMed ID: 3177451
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.