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 *

245 related articles for article (PubMed ID: 6955257)

  • 21. Study of a family with a fragile site of the X chromosome at Xq27-28 without mental retardation.
    Voelckel MA; Philip N; Piquet C; Pellissier MC; Oberlé I; Birg F; Mattei MG; Mattei JF
    Hum Genet; 1989 Mar; 81(4):353-7. PubMed ID: 2564838
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Three families with high expression of a fragile site at Xq27.3, lack of anomalies at the FMR-1 CpG island, and no clear phenotypic association.
    Oberlé I; Boué J; Croquette MF; Voelckel MA; Mattei MG; Mandel JL
    Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):224-31. PubMed ID: 1605195
    [TBL] [Abstract][Full Text] [Related]  

  • 23. X-linked mental retardation with a fragile site in Xq and an inversion of chromosome no. 9.
    Howard-Peebles PN
    Hum Hered; 1982; 32(2):139-41. PubMed ID: 7201453
    [TBL] [Abstract][Full Text] [Related]  

  • 24. X-linked mental retardation, macro-orchidism, and the Xq27 fragile site.
    Turner G; Daniel A; Frost M
    J Pediatr; 1980 May; 96(5):837-41. PubMed ID: 7189210
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. 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]  

  • 27. DNA studies of X-linked mental retardation associated with a fragile site at Xq27.
    Davies KE
    Am J Med Genet; 1986; 23(1-2):633-42. PubMed ID: 3513572
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Fragile sites in human chromosomes II: demonstration of the fragile site Xq27 in carriers of X-linked mental retardation.
    Howard-Peebles PN
    Am J Med Genet; 1980; 7(4):497-501. PubMed ID: 6938133
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Effect of X inactivation on fragile X frequency and mental retardation.
    Rosenberg C; Vianna-Morgante AM; Otto PA; Navajas L
    Am J Med Genet; 1991; 38(2-3):421-4. PubMed ID: 2018084
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Relationship of expansion of CGG repeats and X-inactivation with expression of fra(X)(q27.3) in heterozygotes.
    Mingroni-Netto RC; Fernandes JG; Vianna-Morgante AM
    Am J Med Genet; 1994 Jul; 51(4):443-6. PubMed ID: 7943014
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. Fragile sites in human chromosomes I. The effect of methionine on the Xq fragile site.
    Howard-Peebles PN; Pryor JC
    Clin Genet; 1981 Apr; 19(4):228-32. PubMed ID: 6944163
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Mental impairment in Martin-Bell syndrome is probably determined by interaction of several genes: simple explanation of phenotypic differences between unaffected and affected males with the same X chromosome.
    Steinbach P
    Hum Genet; 1986 Mar; 72(3):248-52. PubMed ID: 3957348
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Transmission of fragile (X) (q27) site from a male.
    Webb GC; Rogers JG; Pitt DB; Halliday J; Theobald T
    Lancet; 1981 Nov; 2(8257):1231-2. PubMed ID: 6118659
    [No Abstract]   [Full Text] [Related]  

  • 35. Frequency of the common fragile site at Xq27.2 under conditions of thymidylate stress: implications for cytogenetic diagnosis of the fragile-X syndrome.
    Ramos FJ; Emanuel BS; Spinner NB
    Am J Med Genet; 1992 Apr; 42(6):835-8. PubMed ID: 1532475
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Segregation of FRAXE in a large family: clinical, psychometric, cytogenetic, and molecular data.
    Hamel BC; Smits AP; de Graaff E; Smeets DF; Schoute F; Eussen BH; Knight SJ; Davies KE; Assman-Hulsmans CF; Oostra BA
    Am J Hum Genet; 1994 Nov; 55(5):923-31. PubMed ID: 7977354
    [TBL] [Abstract][Full Text] [Related]  

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

  • 38. Two families with Xq27.3 fragility, no detectable insert in the FMR-1 gene, mild mental impairment, and absence of the Martin-Bell phenotype.
    Dennis NR; Curtis G; Macpherson JN; Jacobs PA
    Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):232-6. PubMed ID: 1605196
    [TBL] [Abstract][Full Text] [Related]  

  • 39. DNA studies of X-linked mental retardation associated with a fragile site at Xq27.3.
    Goonewardena P; Dahl N; Gustavson KH; Holmgren G; Pettersson U
    Ups J Med Sci Suppl; 1987; 44():155-64. PubMed ID: 2895524
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Familial mental retardation and the fragile X syndrome].
    Veenema H; Pelckmans AJ; Geraedts JP; Van Leeuwen I; Zvelebil N
    Tijdschr Kindergeneeskd; 1984 Feb; 52(1):9-15. PubMed ID: 6585033
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.