BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

126 related articles for article (PubMed ID: 3177453)

  • 1. X-linked mental retardation associated with psoriasis: a new syndrome?
    Tranebjaerg L; Svejgaard A; Lykkesfeldt G
    Am J Med Genet; 1988; 30(1-2):263-73. PubMed ID: 3177453
    [TBL] [Abstract][Full Text] [Related]  

  • 2. New X-linked syndrome with seizures, acquired micrencephaly, and agenesis of the corpus callosum.
    Proud VK; Levine C; Carpenter NJ
    Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):458-66. PubMed ID: 1605226
    [TBL] [Abstract][Full Text] [Related]  

  • 3. New X-linked syndrome with apraxia, ataxia, and mental deficiency: clinical, cytogenetic and neuropsychological studies in two Danish families.
    Tranebjaerg L; Lou H; Andresen J
    Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):498-504. PubMed ID: 1605232
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A new syndrome with mental retardation, short stature and an Xq duplication.
    Thode A; Partington MW; Yip MY; Chapman C; Richardson VF; Turner G
    Am J Med Genet; 1988; 30(1-2):239-50. PubMed ID: 3177451
    [TBL] [Abstract][Full Text] [Related]  

  • 5. X-linked mental retardation with seizures and carrier manifestations is caused by a mutation in the creatine-transporter gene (SLC6A8) located in Xq28.
    Hahn KA; Salomons GS; Tackels-Horne D; Wood TC; Taylor HA; Schroer RJ; Lubs HA; Jakobs C; Olson RL; Holden KR; Stevenson RE; Schwartz CE
    Am J Hum Genet; 2002 May; 70(5):1349-56. PubMed ID: 11898126
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Heritable fragile sites on human chromosomes. III. Detection of fra(X)(q27) in males with X-linked mental retardation and in their female relatives.
    Sutherland GR
    Hum Genet; 1979; 53(1):23-7. PubMed ID: 535898
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A marker X chromosome associated with nonspecific male mental retardation. The first South African cases.
    Venter PA; Gericke GS; Dawson B; Op't Hof J
    S Afr Med J; 1981 Nov; 60(21):807-11. PubMed ID: 7302747
    [TBL] [Abstract][Full Text] [Related]  

  • 8. New X-linked mental retardation disorder with Dandy-Walker malformation, basal ganglia disease, and seizures.
    Pettigrew AL; Jackson LG; Ledbetter DH
    Am J Med Genet; 1991; 38(2-3):200-7. PubMed ID: 2018058
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A new X linked recessive syndrome of mental retardation and mild dysmorphism maps to Xq28.
    Pai GS; Hane B; Joseph M; Nelson R; Hammond LS; Arena JF; Lubs HA; Stevenson RE; Schwartz CE
    J Med Genet; 1997 Jul; 34(7):529-34. PubMed ID: 9222958
    [TBL] [Abstract][Full Text] [Related]  

  • 10. X-linked intellectual handicap and precocious puberty with obesity in carrier females.
    Hockey A
    Am J Med Genet; 1986; 23(1-2):127-37. PubMed ID: 3953642
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The non-deletion alpha thalassaemia/mental retardation syndrome: further support for X linkage.
    Donnai D; Clayton-Smith J; Gibbons RJ; Higgs DR
    J Med Genet; 1991 Nov; 28(11):742-5. PubMed ID: 1770530
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22.
    Tranebjaerg L; Schwartz C; Eriksen H; Andreasson S; Ponjavic V; Dahl A; Stevenson RE; May M; Arena F; Barker D
    J Med Genet; 1995 Apr; 32(4):257-63. PubMed ID: 7643352
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Use of linkage data obtained in single families: prenatal diagnosis of a new X-linked mental retardation syndrome.
    Mulley JC; Gedeon AK; Wilson S; Haan EA
    Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):415-9. PubMed ID: 1605220
    [TBL] [Abstract][Full Text] [Related]  

  • 14. X-linked mental retardation with bilateral clasped thumbs: report of another affected family.
    Straussberg R; Blatt I; Brand N; Kessler D; Katznelson MB; Goodman RM
    Clin Genet; 1991 Nov; 40(5):337-41. PubMed ID: 1756607
    [TBL] [Abstract][Full Text] [Related]  

  • 15. X linked alpha thalassaemia/mental retardation: spectrum of clinical features in three related males.
    Wilkie AO; Gibbons RJ; Higgs DR; Pembrey ME
    J Med Genet; 1991 Nov; 28(11):738-41. PubMed ID: 1770529
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Expression in fibroblast culture of the satellited-X chromosome associated with familial sex-linked mental retardation.
    Jacky PB; Dill FJ
    Hum Genet; 1980 Feb; 53(2):267-9. PubMed ID: 6928413
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. A new X-linked mental retardation syndrome.
    Homfray T; Holland T; Patton M
    Clin Dysmorphol; 1995 Oct; 4(4):289-93. PubMed ID: 8574418
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Fragile site Xq27 and mental retardation. Clinical and cytogenetic manifestation in heterozygotes and hemizygotes of five kindreds.
    Schmidt A
    Hum Genet; 1982; 60(4):322-7. PubMed ID: 6955257
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The 'fragile' X chromosome in the Martin-Bell-Renpenning syndrome and in males with other forms of familial mental retardation.
    Proops R; Webb T
    J Med Genet; 1981 Oct; 18(5):366-73. PubMed ID: 7328617
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.