BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

144 related articles for article (PubMed ID: 4061771)

  • 21. On the genetics of Rett syndrome: analysis of family and pedigree data.
    Killian W
    Am J Med Genet Suppl; 1986; 1():369-76. PubMed ID: 3087198
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Apparent homozygosity for the fragile site at Xq28 in a normal female.
    Nielsen KB; Tommerup N; Poulsen H; Mikkelsen M
    Hum Genet; 1982; 61(1):60-2. PubMed ID: 7129428
    [No Abstract]   [Full Text] [Related]  

  • 23. 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]  

  • 24. The association between Coffin-Lowry syndrome and psychosis: a family study.
    Sivagamasundari U; Fernando H; Jardine P; Rao JM; Lunt P; Jayewardene SL
    J Intellect Disabil Res; 1994 Oct; 38 ( Pt 5)():469-73. PubMed ID: 7841685
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Rett syndrome--search for genetic markers.
    Hanefeld F; Hanefeld U; Wilichowski E; Schmidtke J
    Am J Med Genet Suppl; 1986; 1():377-82. PubMed ID: 3087199
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Prevalence of fragile X-chromosome.
    Lancet; 1984 Jan; 1(8370):220-1. PubMed ID: 6141356
    [No Abstract]   [Full Text] [Related]  

  • 27. 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]  

  • 28. Is there a fragile(X) negative Martin-Bell syndrome?
    Thode A; Laing S; Partington MW; Turner G
    Am J Med Genet; 1988; 30(1-2):459-71. PubMed ID: 3052069
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. 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]  

  • 31. [Phenotypic screening for X-linked mental retardation: fragile Xq syndrome].
    Lacassie I; Zavala AB; Curotto B; Alliende MA; De Andraca I
    Rev Chil Pediatr; 1982; 53(5):419-25. PubMed ID: 7182864
    [No Abstract]   [Full Text] [Related]  

  • 32. Fragile X syndrome: a unique mutation in man.
    Nussbaum RL; Ledbetter DH
    Annu Rev Genet; 1986; 20():109-45. PubMed ID: 3545058
    [No Abstract]   [Full Text] [Related]  

  • 33. 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]  

  • 34. 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]  

  • 35. Neuropsychiatric disturbances in a patient with a nonmosaic isodicentric (X) (q21.32) chromosome.
    Suzuki T; Koizumi J; Arinami T; Shiraishi H; Ofuku K; Kawai N; Baba A; Ninomiya H
    Jpn J Psychiatry Neurol; 1990 Sep; 44(3):563-70. PubMed ID: 2127433
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A study of autism using X chromosome DNA probes.
    Crowe RR; Tsai LY; Murray JC; Patil SR; Quinn J
    Biol Psychiatry; 1988 Aug; 24(4):473-9. PubMed ID: 3408765
    [No Abstract]   [Full Text] [Related]  

  • 37. Klinefelter syndrome and two fragile X chromosomes.
    Fryns JP; Kleczkowska A; Wolfs I; van den Berghe H
    Clin Genet; 1984 Nov; 26(5):445-7. PubMed ID: 6499257
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The strength of association between fragile (X) chromosome presence and mental retardation.
    Silverman W; Lubin R; Jenkins EC; Brown WT
    Clin Genet; 1983 Jun; 23(6):436-40. PubMed ID: 6684008
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A family with fragile-X syndrome.
    Kerbeshian J; Burd L; Martsolf J
    J Nerv Ment Dis; 1984 Sep; 172(9):549-51. PubMed ID: 6590782
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 8.