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 *

177 related articles for article (PubMed ID: 6141356)

  • 21. Chromosome studies in 10 patients with the Rett syndrome.
    Moore JW; Tuck-Muller CM; Murphy M; Naidu S; Thomas GH
    Am J Med Genet Suppl; 1986; 1():345-54. PubMed ID: 3087195
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The inactivation of the fragile X chromosome in female carriers of the Martin Bell syndrome as studied by two different methods.
    Tuckerman E; Webb T
    Clin Genet; 1989 Jul; 36(1):25-30. PubMed ID: 2766560
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Fragile X trait in a large kindred: transmission also through normal males.
    Van Roy BC; De Smedt MC; Raes RA; Dumon JE; Leroy JG
    J Med Genet; 1983 Aug; 20(4):286-9. PubMed ID: 6620329
    [TBL] [Abstract][Full Text] [Related]  

  • 24. No significant relationship between age and frequency of chromosome lesions in mentally retarded individuals with or without the fragile X syndrome.
    Butler MG
    Hum Genet; 1990 Jan; 84(2):216-7. PubMed ID: 2298460
    [No Abstract]   [Full Text] [Related]  

  • 25. The fragile (X) syndrome: the mutation problem.
    Jacobs PA; Sherman S; Turner G; Webb T
    Am J Med Genet; 1986; 23(1-2):611-7. PubMed ID: 3953671
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Rett syndrome: lack of association with fragile site Xp22 and strategy for genetic mapping of X-linked new mutations.
    Romeo G; Archidiacono N; Ferlini A; Rocchi M
    Am J Med Genet Suppl; 1986; 1():355-9. PubMed ID: 3087196
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A cytogenetic study of a population of retarded females with special reference to the fragile (X) syndrome.
    Mayer M; Abruzzo MA; Jacobs PA; Yee SC
    Hum Genet; 1985; 69(3):206-8. PubMed ID: 3980014
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Molecular genetics of the human X chromosome.
    Davies KE
    J Med Genet; 1985 Aug; 22(4):243-9. PubMed ID: 2995673
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. 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]  

  • 32. 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]  

  • 33. RFLP for linkage analysis of fragile X syndrome.
    Brown WT; Wu Y; Gross AC; Chan CB; Dobkin CS; Jenkins EC
    Lancet; 1987 Jan; 1(8527):280. PubMed ID: 2880102
    [No Abstract]   [Full Text] [Related]  

  • 34. Unusual X chromosome inactivation in a mentally retarded girl with an interstitial deletion Xq27: implications for the fragile X syndrome.
    Schmidt M; Certoma A; Du Sart D; Kalitsis P; Leversha M; Fowler K; Sheffield L; Jack I; Danks DM
    Hum Genet; 1990 Mar; 84(4):347-52. PubMed ID: 2307456
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Interpretation of the heterogeneity in the linkage relationships of DNA markers around the fragile X locus.
    Winter R; Pembrey M
    Hum Genet; 1987 Nov; 77(3):297-8. PubMed ID: 3479389
    [No Abstract]   [Full Text] [Related]  

  • 36. Dermatoglyphic findings in patients with fragile X-chromosome.
    Hirth L; Singh S; Schilling S; Müller E; Goedde HW
    Clin Genet; 1985 Feb; 27(2):118-21. PubMed ID: 3978845
    [TBL] [Abstract][Full Text] [Related]  

  • 37. X linked mental retardation: a family with a separate syndrome?
    Thompson EM; Gordon A; Baraitser M
    J Med Genet; 1989 Jun; 26(6):373-8. PubMed ID: 2738899
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Chromosomal aberrations in the mildly mentally retarded.
    Göstason R; Wahlström J; Johannisson T; Holmqvist D
    J Ment Defic Res; 1991 Jun; 35 ( Pt 3)():240-6. PubMed ID: 1833552
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Further segregation analysis of the fragile X syndrome with special reference to transmitting males.
    Pembrey ME; Winter RM
    Hum Genet; 1985; 71(2):182-3. PubMed ID: 4043970
    [No Abstract]   [Full Text] [Related]  

  • 40. Genetic mapping of the human X chromosome: linkage analysis of the q26-q28 region that includes the fragile X locus and isolation of expressed sequences.
    Mandel JL; Arveiler B; Camerino G; Hanauer A; Heilig R; Koenig M; Oberlé I
    Cold Spring Harb Symp Quant Biol; 1986; 51 Pt 1():195-203. PubMed ID: 3472716
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.