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 *

243 related articles for article (PubMed ID: 3052069)

  • 1. 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]  

  • 2. Normal male carriers in the fra(X) form of X-linked mental retardation (Martin-Bell syndrome).
    Froster-Iskenius U; McGillivray BC; Dill FJ; Hall JG; Herbst DS
    Am J Med Genet; 1986; 23(1-2):619-31. PubMed ID: 3953672
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The strength of association between fragile (X) chromosome presence and mental retardation.
    Silverman W; Lubin R; Jenkins EC; Brown WT
    Clin Genet; 1983 Jun; 23(6):436-40. PubMed ID: 6684008
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. The fragile X-chromosome: an evaluation of the results in a routine cytogenetic laboratory in the period 1981-1986.
    Veenema H; Beverstock GC; de Koning T; Pearson PL; van de Kamp JJ
    Clin Genet; 1988 Jun; 33(6):410-7. PubMed ID: 3168313
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Investigation of the segregation of the fragile X mutation in daughters of obligate carrier women.
    Sherman SL; Turner G; Robinson H; Laing S
    Am J Med Genet; 1988; 30(1-2):633-9. PubMed ID: 3177475
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Fragile X-linked mental retardation: the Martin-Bell syndrome.
    Richards BW; Sylvester PE; Brooker C
    J Ment Defic Res; 1981 Dec; 25 Pt 4():253-6. PubMed ID: 7328634
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cytogenetically negative, linkage positive "fragile X" syndrome.
    Sklower Brooks S; Cohen I; Ferrando C; Jenkins EC; Brown WT; Dobkin C
    Am J Med Genet; 1991; 38(2-3):370-3. PubMed ID: 1673313
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic heterogeneity of X-linked mental retardation with fragile X. Association of tight linkage to factor IX and incomplete penetrance in males.
    Giannelli F; Morris AH; Garrett C; Daker M; Thurston C; Smith CA
    Ann Hum Genet; 1987 May; 51(2):107-24. PubMed ID: 3674751
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Clinical and cytogenetic diagnosis of Martin-Bell syndrome].
    Kupriianova TA; Gor'kova SA; Marincheva GS
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1991; 91(8):49-53. PubMed ID: 1661516
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Frequency of the fragile X syndrome in Japanese mentally retarded males.
    Arinami T; Kondo I; Nakajima S
    Hum Genet; 1986 Aug; 73(4):309-12. PubMed ID: 3744362
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Fragile X mental retardation: prevalence in a group of institutionalized patients in Italy and description of a novel EEG pattern.
    Sanfilippo S; Ragusa RM; Musumeci S; Neri G
    Am J Med Genet; 1986; 23(1-2):589-95. PubMed ID: 3953669
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The fragile X syndrome I: familial variation in the proportion of lymphocytes with the fragile site in males.
    Soudek D; Partington MW; Lawson JS
    Am J Med Genet; 1984 Jan; 17(1):241-52. PubMed ID: 6711598
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Fragile X syndrome with extra microchromosome.
    López-Pajares I; Delicado A; Pascual-Castroviejo I; López-Martin V; Moreno F; Garcia-Marcos JA
    Clin Genet; 1994 Apr; 45(4):186-9. PubMed ID: 8062436
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. A clinical, cytogenetic and familial study of 307 mentally retarded, institutionalized, adult male patients with special interest for fra(X) negative X-linked mental retardation.
    Haspeslagh M; Fryns JP; Holvoet M; Collen G; Dierck G; Baeke J; van den Berghe H
    Clin Genet; 1991 Jun; 39(6):434-41. PubMed ID: 1863991
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Martin-Bell syndrome fra(X) (q28) in a Sri Lankan family.
    Soysa P; Senanayahe M; Mikkelsen M; Poulsen H
    J Ment Defic Res; 1982 Dec; 26 (Pt 4)():251-7. PubMed ID: 7169632
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.