BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

438 related articles for article (PubMed ID: 3843245)

  • 1. 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]  

  • 2. X-linked mental retardation. I. Martin-Bell syndrome (report of 18 families).
    Rocchi M; Archidiacono N; Filippi G
    J Genet Hum; 1987 Dec; 35(5):351-79. PubMed ID: 3437265
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Martin-Bell syndrome in Greece, with report of another 47,XXY fragile X patient.
    Mavrou A; Syrrou M; Tsenghi C; Agelakis M; Youroukos S; Metaxotou C
    Am J Med Genet; 1988 Dec; 31(4):735-9. PubMed ID: 3239562
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Fragile X mutation and FG syndrome-like phenotype.
    Piussan C; Mathieu M; Berquin P; Fryns JP
    Am J Med Genet; 1996 Aug; 64(2):395-8. PubMed ID: 8844090
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The diagnosis and frequency of X-linked conditions in a cohort of moderately retarded males with affected brothers.
    Fishburn J; Turner G; Daniel A; Brookwell R
    Am J Med Genet; 1983 Apr; 14(4):713-24. PubMed ID: 6682625
    [TBL] [Abstract][Full Text] [Related]  

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

  • 7. [The fragile X (Martin-Bell) syndrome].
    Zergollern-Cupak L; Sabol Z; Hitrec V; Vuković J; Medica I
    Lijec Vjesn; 1990; 112(11-12):393-6. PubMed ID: 2097475
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. [Mental retardation and fragile X chromosome. Clinical and cytogenetic study of 3 families].
    Gilgenkrantz S; Boué J; Grégoire MJ; Tejada I
    J Genet Hum; 1984 Jul; 32(3):199-207. PubMed ID: 6481342
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetics and expression of the fragile X syndrome.
    Brown WT; Jenkins EC; Gross AC; Chan CB; Wisniewski K; Cohen IL; Miezejeski CM
    Ups J Med Sci Suppl; 1987; 44():137-54. PubMed ID: 2895523
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [X-linked mental retardation, macro-orchism, and X chromosome fragile site. Presentation of 6 cases in 2 families].
    Pascual-Castroviejo I; López Pajares I; Delicado A
    An Esp Pediatr; 1982 Dec; 17(6):466-74. PubMed ID: 6892145
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Fragile X syndrome.
    Laxova R
    Adv Pediatr; 1994; 41():305-42. PubMed ID: 7992687
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [X chromosome-linked mental retardation with fragile X chromosome and macro-orchidism].
    Zollinger A; Schmid W; Vilan J; Sorg B; Knoblauch M
    Schweiz Med Wochenschr; 1983 Feb; 113(7):238-44. PubMed ID: 6836249
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Fragile-X syndrome ascertained by the presence of macro-orchidism in a 5-month-old infant.
    Carmi R; Meryash DL; Wood J; Gerald PS
    Pediatrics; 1984 Nov; 74(5):883-6. PubMed ID: 6493884
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Phenotypic variation in male-transmitted fragile X: genetic inferences.
    Loesch DZ; Hay DA; Sutherland GR; Halliday J; Judge C; Webb GC
    Am J Med Genet; 1987 Jun; 27(2):401-17. PubMed ID: 3605224
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Fragile X frequency in a mentally retarded population in Brazil.
    Mingroni-Netto RC; Rosenberg C; Vianna-Morgante AM; Pavanello Rde C
    Am J Med Genet; 1990 Jan; 35(1):22-7. PubMed ID: 2301469
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Mental deficiency associated with a fragility of the X chromosome].
    Guitart Feliubadalo M; Artigas Pallarés J; Fuster Marqués C; Gabau Vila E; Lorente Hurtado I; Argemí Renom J
    An Esp Pediatr; 1988 Nov; 29(5):377-81. PubMed ID: 3232895
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Fragile X syndrome: a common etiology of mental retardation.
    Rogers RC; Simensen RJ
    Am J Ment Defic; 1987 Mar; 91(5):445-9. PubMed ID: 3565490
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Fragile X-linked mental retardation. A survey of 65 patients with mental retardation of unknown origin.
    Carpenter NJ; Leichtman LG; Say B
    Am J Dis Child; 1982 May; 136(5):392-8. PubMed ID: 7081157
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 22.