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 *

128 related articles for article (PubMed ID: 3087199)

  • 21. Marker X-associated mental retardation. A study of 150 retarded males.
    Kähkönen M; Leisti J; Wilska M; Varonen S
    Clin Genet; 1983 Jun; 23(6):397-404. PubMed ID: 6576874
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Specificity of PCR-SSCP for detection of the mutant ornithine transcarbamylase (OTC) gene in patients with OTC deficiency.
    Hoshide R; Matsuura T; Komaki S; Koike E; Ueno I; Matsuda I
    J Inherit Metab Dis; 1993; 16(5):857-62. PubMed ID: 8295401
    [No Abstract]   [Full Text] [Related]  

  • 23. Clinical recognition of Rett syndrome.
    Philippart M
    Am J Med Genet Suppl; 1986; 1():111-8. PubMed ID: 3087171
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [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]  

  • 25. A 5-megabase familial deletion removes the IDS and FMR-1 genes in a male Hunter patient.
    Birot AM; Delobel B; Gronnier P; Bonnet V; Maire I; Bozon D
    Hum Mutat; 1996; 7(3):266-8. PubMed ID: 8829661
    [No Abstract]   [Full Text] [Related]  

  • 26. Extrapyramidal involvement in Rett's syndrome.
    FitzGerald PM; Jankovic J; Glaze DG; Schultz R; Percy AK
    Neurology; 1990 Feb; 40(2):293-5. PubMed ID: 2073236
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Seventh International Workshop on the Fragile X and X-linked Mental Retardation.
    Tranebjaerg L; Lubs HA; Borghgraef M; Brown WT; Fisch G; Fryns JP; Hagerman R; Jacobs PA; Mandel JL; Mulley J; Oostra B; Schwartz C; Sherman S; Willard H; Willems P
    Am J Med Genet; 1996 Jul; 64(1):1-14. PubMed ID: 8826442
    [No Abstract]   [Full Text] [Related]  

  • 29. Fragile X positivity in Chinese children with autistic spectrum disorder.
    Wong VC; Lam ST
    Pediatr Neurol; 1992; 8(4):272-4. PubMed ID: 1388415
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Survey of adolescents with severe intellectual handicap.
    Asthana JC; Sinha S; Haslam JS; Kingston HM
    Arch Dis Child; 1990 Oct; 65(10):1133-6. PubMed ID: 2248505
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 9th international workshop on fragile X syndrome and X-linked mental retardation.
    Fryns JP; Borghgraef M; Brown TW; Chelly J; Fisch GS; Hamel B; Hanauer A; Lacombe D; Luo L; MacPherson JN; Mandel JL; Moraine C; Mulley J; Nelson D; Oostra B; Partington M; Ramakers GJ; Ropers HH; Rousseau F; Schwartz C; Steinbach P; Stoll C; Tranebjaerg L; Turner G; Van Bokhoven H; Vianna-Morgante A
    Am J Med Genet; 2000 Oct; 94(5):345-60. PubMed ID: 11050616
    [No Abstract]   [Full Text] [Related]  

  • 32. Genetic analysis of the fragile-X mental retardation syndrome with two flanking polymorphic DNA markers.
    Oberlé I; Heilig R; Moisan JP; Kloepfer C; Mattéi GM; Mattéi JF; Boué J; Froster-Iskenius U; Jacobs PA; Lathrop GM
    Proc Natl Acad Sci U S A; 1986 Feb; 83(4):1016-20. PubMed ID: 3006023
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Rett's syndrome in the west of Scotland.
    Kerr AM; Stephenson JB
    Br Med J (Clin Res Ed); 1985 Aug; 291(6495):579-82. PubMed ID: 2412628
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Non-specific X-linked mental retardation: background, types, diagnosis and prevalence.
    Howard-Peebles PN
    J Ment Defic Res; 1982 Dec; 26 (Pt 4)():205-13. PubMed ID: 6763078
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A cytogenetic study in 120 Turkish children with intellectual disability and characteristics of fragile X syndrome.
    Demirhan O; Taştemir D; Diler RS; Firat S; Avci A
    Yonsei Med J; 2003 Aug; 44(4):583-92. PubMed ID: 12950112
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Fragile X syndrome in mildly mentally retarded children in a northern Swedish county. A prevalence study.
    Blomquist HK; Gustavson KH; Holmgren G; Nordenson I; Pålsson-Stråe U
    Clin Genet; 1983 Dec; 24(6):393-8. PubMed ID: 6652951
    [TBL] [Abstract][Full Text] [Related]  

  • 37. X-linked mental retardation with the fragile X. A study of 15 families.
    Mattei JF; Mattei MG; Aumeras C; Auger M; Giraud F
    Hum Genet; 1981; 59(4):281-9. PubMed ID: 7333582
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Ornithine transcarbamylase (OTC) deficiency in a female patient with a de nova deletion of the paternal X chromosome.
    Slomski R; Braulke I; Behrend C; Schröder E; Colombo JP; Reiss J
    Hum Genet; 1992 Aug; 89(6):632-4. PubMed ID: 1511981
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Conference report: Fourth International Workshop on the fragile X and X-linked mental retardation.
    Brown WT; Jenkins E; Neri G; Lubs H; Shapiro LR; Davies KE; Sherman S; Hagerman R; Laird C
    Am J Med Genet; 1991; 38(2-3):158-72. PubMed ID: 1673296
    [No Abstract]   [Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 7.