BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

100 related articles for article (PubMed ID: 2163175)

  • 1. [Clinico-electrophysiological examination of children with Martin-Bell syndrome].
    Lastochkina NA; Kuprianova TA; Puchinskaia LM; Marincheva GS
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1990; 90(3):69-75. PubMed ID: 2163175
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [The role of the marker X chromosome in the diagnosis of Martin-Bell syndrome (review of the literature)].
    Bessudnova SS; Il'inskikh NN
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1990; 90(3):128-32. PubMed ID: 2163154
    [No Abstract]   [Full Text] [Related]  

  • 3. [Electrophysiological study of children with various hereditary forms of mental retardation].
    Puchinskaia LM; Lastochkina NA; Marincheva GS
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1989; 89(3):51-7. PubMed ID: 2728749
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Possibility of EEG-diagnosis of heterozygotic Martin-Bell syndrome].
    Moskovkina AG; Blagosklonova NK
    Genetika; 1990 Oct; 26(10):1865-9. PubMed ID: 2283054
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Variable expression of clinical features of Martin Bell syndrome in younger patients.
    Verma IC; Elango R
    Indian Pediatr; 1994 Apr; 31(4):433-8. PubMed ID: 7875865
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Clinico-electrophysiological characteristics of women--heterozygote carriers of fragile X chromosome].
    Lastochkina NA; Kupriianova TA; Puchinskaia LM; Marincheva GS; Gor'kova SA
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1992; 92(4):28-31. PubMed ID: 1333701
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Fragile X mental retardation syndrome: from pathogenesis to diagnostic issues.
    Mandel JL; Biancalana V
    Growth Horm IGF Res; 2004 Jun; 14 Suppl A():S158-65. PubMed ID: 15135801
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Martin-Bell syndrome (mental retardation with fragile X syndrome (review of the literature)].
    Kuprianova TA
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1991; 91(8):115-25. PubMed ID: 1661501
    [No Abstract]   [Full Text] [Related]  

  • 10. [The importance of molecular genetic diagnosis of Martin-Bell disease in genetic counseling].
    Horváth M; Tímár L; Karcagi V; Czeizel E
    Orv Hetil; 1997 Mar; 138(9):541-5. PubMed ID: 9102630
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Clinical manifestations of oligophrenia with fragile X syndrome in boys in the pre- and post-pubertal age].
    Bliumina MG
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1989; 89(8):101-5. PubMed ID: 2588887
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Sex-related neurologic diseases. Familial X-linked mental retardation with a fragile X marker. Study of 8 families].
    Rodríguez Costa T; Gabarrón Llamas J; Casas Fernández C; Glover López G; Puche Mira A; Jiménez Cocina A
    An Esp Pediatr; 1984 Oct; 21 Suppl 20():54-7. PubMed ID: 6595955
    [No Abstract]   [Full Text] [Related]  

  • 13. [Clinical and cytogenetic problems in diagnosis of fragile X syndrome].
    von Gontard A; Hillig U; Herold D
    Z Kinder Jugendpsychiatr; 1992 Jun; 20(2):113-20. PubMed ID: 1509819
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Fragile X and Martin-Bell syndrome: new source of information.
    Barbi G; Steinbach P
    Am J Med Genet; 1985 Oct; 22(2):415-6. PubMed ID: 4050871
    [No Abstract]   [Full Text] [Related]  

  • 15. 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]  

  • 16. [Fragile X chromosome and autistic mental retardation. Apropos of 23 cases].
    Bénézech M; Noel B; Noel L; Bourgeois M
    Ann Med Psychol (Paris); 1983 Nov; 141(9):1006-11. PubMed ID: 6666917
    [No Abstract]   [Full Text] [Related]  

  • 17. [Are there reproducible false-positive fra(X) findings in differential diagnosis of Martin-Bell syndrome?].
    Kennerknecht I; Barbi G; Steinbach P
    Z Kinder Jugendpsychiatr; 1991; 19(3):204-6. PubMed ID: 1962515
    [No Abstract]   [Full Text] [Related]  

  • 18. Status epilepticus in fragile X syndrome.
    Gauthey M; Poloni CB; Ramelli GP; Roulet-Perez E; Korff CM
    Epilepsia; 2010 Dec; 51(12):2470-3. PubMed ID: 21204809
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A deletion of 1.6 Kb proximal to the CGG repeat of the FMR1 gene causes fragile X-like psychological features.
    Wiegers AM; Curfs LM; Meijer H; Oostra B; Fryns JP
    Genet Couns; 1994; 5(4):377-80. PubMed ID: 7888141
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 5.