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 *

432 related articles for article (PubMed ID: 6607708)

  • 1. XY/XXY mosaicism and fragile X syndrome.
    Fryns JP; Kleczkowska A; Kubień E; Petit P; Haspeslagh M; Lindemans I; Van Den Berghe H
    Ann Genet; 1983; 26(4):251-3. PubMed ID: 6607708
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Cytogenetic findings in moderate and severe mental retardation. A study of an institutionalized population of 1991 patients.
    Fryns JP; Kleczkowska A; Kubień E; Van den Berghe H
    Acta Paediatr Scand Suppl; 1984; 313():1-23. PubMed ID: 6241420
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Cytogenetic study of 257 mentally deficient patients in psychiatric hospitals].
    Bourgeois M; Bénézech M; Tournier-Zerbid N; Constant-Boy M; Benazet-Rissou J
    Ann Med Psychol (Paris); 1975 Nov; 2(4):756-82. PubMed ID: 135524
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Mosaic status in lymphocytes of infertile men with or without Klinefelter syndrome.
    Lenz P; Luetjens CM; Kamischke A; Kühnert B; Kennerknecht I; Nieschlag E
    Hum Reprod; 2005 May; 20(5):1248-55. PubMed ID: 15665007
    [TBL] [Abstract][Full Text] [Related]  

  • 6. X-linked mental retardation.
    Fryns JP
    Prog Clin Biol Res; 1985; 177():309-19. PubMed ID: 2409559
    [No Abstract]   [Full Text] [Related]  

  • 7. Rare XXY/XX mosaicism in a phenotypic male with Klinefelter syndrome: case report.
    Velissariou V; Christopoulou S; Karadimas C; Pihos I; Kanaka-Gantenbein C; Kapranos N; Kallipolitis G; Hatzaki A
    Eur J Med Genet; 2006; 49(4):331-7. PubMed ID: 16829354
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A variant Klinefelter syndrome patient with an XXY/XX/XY karyotype studied by GTG-banding and fluorescence in situ hybridization.
    Mark HF; Bai H; Sotomayor E; Mark S; Zolnierz K; Airall E; Sigman M
    Exp Mol Pathol; 1999 Sep; 67(1):50-6. PubMed ID: 10493892
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 46,XY/47,XYY male with the fragile X syndrome: cytogenetic and molecular studies.
    Milunsky A; Huang X; Amos JA; Herskowitz J; Farrer LA; Wyandt HE
    Am J Med Genet; 1993 Mar; 45(5):589-93. PubMed ID: 8096117
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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]  

  • 11. The marker Xq28 syndrome ("Fragile-X SYndrome") in a retarded man with mitral valve prolapse.
    Pyeritz RE; Stamberg J; Thomas GH; Bell BB; Zahka KG; Bernhardt BA
    Johns Hopkins Med J; 1982 Nov; 151(5):231-7. PubMed ID: 6958915
    [No Abstract]   [Full Text] [Related]  

  • 12. [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]  

  • 13. [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]  

  • 14. [Molecular cytogenetic diagnosis of Klinefelter's syndrome in men more frequently detects sex chromosome mosaicism than classical cytogenetic methods].
    Kurková S; Zemanová Z; Hána V; Mayerová K; Pacovská K; Musilová J; Stĕpán J; Michalová K
    Cas Lek Cesk; 1999 Apr; 138(8):235-8. PubMed ID: 10510542
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [(Fra)X in male cousins with mental retardation].
    Rozynkowa D; Górski G; Jabłońska R
    Pediatr Pol; 1986 Jul; 61(7):441-5. PubMed ID: 3822610
    [No Abstract]   [Full Text] [Related]  

  • 16. 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]  

  • 17. Fragile X syndrome associated with Tourette symptomatology in a male with moderate mental retardation and autism.
    Kerbeshian J; Burd L; Martsolf JT
    J Dev Behav Pediatr; 1984 Aug; 5(4):201-3. PubMed ID: 6590572
    [No 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. [Recombination between the fragile site Xq27 and the gene for coagulation factor IX].
    Landoulsi A; de Blois MC; Guérin P; Rethoré MO; Lejeune J; Lucotte G
    Ann Genet; 1985; 28(4):201-5. PubMed ID: 3879429
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [The fragile X syndrome and its relation to other chromosome X-linked syndromes that are associated with mental retardation].
    Prieto F; Martínez-Castellano F
    Med Clin (Barc); 1992 Feb; 98(4):131-3. PubMed ID: 1552762
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 22.