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 *

135 related articles for article (PubMed ID: 3758508)

  • 21. 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]  

  • 22. X-linked mental retardation and characteristic physical features in two brothers with duplication Xp22-Xpter.
    Cianchetti C; Muntoni F; Falchi AM; Nucaro A; Sannio-Fancello G; Cao A; Marrosu MG
    Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):475-8. PubMed ID: 1605229
    [TBL] [Abstract][Full Text] [Related]  

  • 23. X linked mental retardation.
    Glass IA
    J Med Genet; 1991 Jun; 28(6):361-71. PubMed ID: 1870092
    [No Abstract]   [Full Text] [Related]  

  • 24. Clinical features of a female with WDR45 mutation complicated by infantile spasms: a case report and literature review.
    Morikawa M; Takano K; Motobayashi M; Shiba N; Kosho T; Nakazawa Y; Inaba Y
    Brain Dev; 2017 Oct; 39(9):804-807. PubMed ID: 28551038
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The non-deletion type of alpha thalassaemia/mental retardation: a recognisable dysmorphic syndrome with X linked inheritance.
    Wilkie AO; Pembrey ME; Gibbons RJ; Higgs DR; Porteous ME; Burn J; Winter RM
    J Med Genet; 1991 Oct; 28(10):724. PubMed ID: 1941971
    [No Abstract]   [Full Text] [Related]  

  • 26. Developmental delay, expressive aphasia, hypotonia and dysmorphism in two brothers: an X-linked mental retardation syndrome?
    Jones KJ; North KN
    Clin Genet; 1998 Nov; 54(5):443-5. PubMed ID: 9843001
    [No Abstract]   [Full Text] [Related]  

  • 27. Sex-linked recessive congenital ataxia.
    Young ID; Moore JR; Tripp JH
    J Neurol Neurosurg Psychiatry; 1987 Sep; 50(9):1230-2. PubMed ID: 3668574
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Linkage to Xq28 in a family with nonspecific X-linked mental retardation.
    Nordström AM; Penttinen M; von Koskull H
    Hum Genet; 1992 Nov; 90(3):263-6. PubMed ID: 1362558
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. X-linked mental retardation: caveats in genetic counselling.
    Partington MW
    Am J Med Genet; 1986; 23(1-2):101-9. PubMed ID: 3953640
    [No Abstract]   [Full Text] [Related]  

  • 31. X-linked mental retardation.
    Turner G
    Psychol Med; 1982 Aug; 12(3):471-3. PubMed ID: 6957904
    [No Abstract]   [Full Text] [Related]  

  • 32. 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]  

  • 33. Physical fine mapping of genes underlying X-linked deafness and non fra (X)-X-linked mental retardation at Xq21.
    Bach I; Robinson D; Thomas N; Ropers HH; Cremers FP
    Hum Genet; 1992 Aug; 89(6):620-4. PubMed ID: 1511979
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Mental retardation. Sex-linked recessive hereditary type of mental retardation-- current genetic and cytogenetic findings].
    Neuhäuser G
    ZFA (Stuttgart); 1982 Dec; 58(34):1861-3. PubMed ID: 6764702
    [No Abstract]   [Full Text] [Related]  

  • 35. Non-specific X linked mental retardation.
    Kerr B; Turner G; Mulley J; Gedeon A; Partington M
    J Med Genet; 1991 Jun; 28(6):378-82. PubMed ID: 1870094
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. X-linked mental retardation with fragile site at band Xq2800.
    Hecht JT; Scott CI; Butler IJ; Moore CM
    Lancet; 1983 Apr; 1(8331):986. PubMed ID: 6132290
    [No Abstract]   [Full Text] [Related]  

  • 38. Bibliography of X-linked mental retardation and related subjects. III. (1986).
    Opitz JM; Holt MC; Spano LM
    Am J Med Genet; 1986; 23(1-2):69-99. PubMed ID: 3513573
    [No Abstract]   [Full Text] [Related]  

  • 39. X-linked recessive nephritis with mental retardation, sensorineural hearing loss, and macrocephaly.
    Lane W; Robson M; Lowry RB; Leung AK
    Clin Genet; 1994 Jun; 45(6):314-7. PubMed ID: 7923864
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The early detection of mental retardation.
    Shapiro BK; Palmer FB; Capute AJ
    Clin Pediatr (Phila); 1987 May; 26(5):215-20. PubMed ID: 3568526
    [No Abstract]   [Full Text] [Related]  

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