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 *

171 related articles for article (PubMed ID: 3177478)

  • 1. Fragile X syndrome: a hypothesis regarding the molecular mechanism of the phenotype.
    Warren ST
    Am J Med Genet; 1988; 30(1-2):681-8. PubMed ID: 3177478
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Inheritance of fragile X syndrome: an hypothesis.
    Friedman JM; Howard-Peebles PN
    Am J Med Genet; 1986; 23(1-2):701-13. PubMed ID: 3006493
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Isolation of the human chromosomal band Xq28 within somatic cell hybrids by fragile X site breakage.
    Warren ST; Knight SJ; Peters JF; Stayton CL; Consalez GG; Zhang FP
    Proc Natl Acad Sci U S A; 1990 May; 87(10):3856-60. PubMed ID: 2339126
    [TBL] [Abstract][Full Text] [Related]  

  • 4. DNA studies of X-linked mental retardation associated with a fragile site at Xq27.3.
    Goonewardena P; Dahl N; Gustavson KH; Holmgren G; Pettersson U
    Ups J Med Sci Suppl; 1987; 44():155-64. PubMed ID: 2895524
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Study of a family with a fragile site of the X chromosome at Xq27-28 without mental retardation.
    Voelckel MA; Philip N; Piquet C; Pellissier MC; Oberlé I; Birg F; Mattei MG; Mattei JF
    Hum Genet; 1989 Mar; 81(4):353-7. PubMed ID: 2564838
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Is there a fragile(X) negative Martin-Bell syndrome?
    Thode A; Laing S; Partington MW; Turner G
    Am J Med Genet; 1988; 30(1-2):459-71. PubMed ID: 3052069
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Expression of the autosomal folate-sensitive fragile sites in ten kindreds with Martin-Bell syndrome.
    Ventruto V; Stabile M; Gentile G; de Tollis G; Colantuoni M; Sirone P; Perone L; Lonardo F; Della Monica M; Fiore M
    Ann Genet; 1986; 29(1):59-61. PubMed ID: 3487280
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Expression of the fragile site Xq27 in fibroblasts. II. Evidence for negative and positive clones from heterozygous females and possible relationship between frequency and phenotype.
    Steinbach P; Barbi G; Baur S; Vogel W
    Hum Genet; 1983; 64(3):279-82. PubMed ID: 6885072
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Fra(X) frequency on the active X-chromosome and phenotype in heterozygous carriers of the fra(X) form of mental retardation.
    Wilhelm D; Froster-Iskenius U; Paul J; Schwinger E
    Am J Med Genet; 1988; 30(1-2):407-15. PubMed ID: 3177461
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The fragile X syndrome in a large family. III. Investigations on linkage of flanking DNA markers with the fragile site Xq27.
    Veenema H; Carpenter NJ; Bakker E; Hofker MH; Ward AM; Pearson PL
    J Med Genet; 1987 Jul; 24(7):413-21. PubMed ID: 2886667
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Pulsed-field gel mapping studies in the vicinity of the fragile site at Xq27.3.
    Patterson M; Bell M; Schwartz C; Davies K
    Am J Med Genet; 1988; 30(1-2):581-91. PubMed ID: 3177471
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A premutation that generates a defect at crossing over explains the inheritance of fragile X mental retardation.
    Pembrey ME; Winter RM; Davies KE
    Am J Med Genet; 1985 Aug; 21(4):709-17. PubMed ID: 4040705
    [TBL] [Abstract][Full Text] [Related]  

  • 13. In situ nick translation of the fragile X region.
    Nolin SL; Jenkins EC; Brown WT; Dobkin CS
    Am J Med Genet; 1988; 30(1-2):443-50. PubMed ID: 3052067
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Encephalopathy related to X fragility: neither inactivation nor deletion of the distal fragment q28 to qter. Enzymatic and morphometric evidence].
    Jalbert H; Baeteman MA; Trochet-Royer C; Mattei MG; Mattei JF; Leroux D; Jalbert P
    J Genet Hum; 1983 Jun; 31(2):133-9. PubMed ID: 6631423
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The fragile X syndrome.
    Brown WT
    Neurol Clin; 1989 Feb; 7(1):107-21. PubMed ID: 2646518
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Fragile (X) X-linked mental retardation. II. Frequency and replication pattern of fragile (X)(q28) in heterozygotes.
    Knoll JH; Chudley AE; Gerrard JW
    Am J Hum Genet; 1984 May; 36(3):640-5. PubMed ID: 6731439
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The fragile X syndrome (Martin-Bell syndrome). Clinical and cytogenetic findings in 16 prepubertal boys and in 4 of their 5 families.
    Schinzel A; Largo RH
    Helv Paediatr Acta; 1985 Jul; 40(2-3):133-52. PubMed ID: 3843245
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Recombination and amplification of pyrimidine-rich sequences may be responsible for initiation and progression of the Xq27 fragile site: an hypothesis.
    Nussbaum RL; Airhart SD; Ledbetter DH
    Am J Med Genet; 1986; 23(1-2):715-21. PubMed ID: 3456708
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mental retardation in heterozygotes for the fragile-X mutation: evidence in favor of an X inactivation-dependent effect.
    Rocchi M; Archidiacono N; Rinaldi A; Filippi G; Bartolucci G; Fancello GS; Siniscalco M
    Am J Hum Genet; 1990 Apr; 46(4):738-43. PubMed ID: 2316520
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Two brothers with mental retardation discordant for the fragile-X syndrome.
    Van Roy BC; Willems PJ; Vits LJ; Ceulemans BP; Coucke PJ; Van der Auwera BJ; Lormans JA; Dumon JE
    Am J Med Genet; 1990 May; 36(1):122-5. PubMed ID: 2333901
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.