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 *

79 related articles for article (PubMed ID: 5019828)

  • 1. [A clinical study of offsprings of oligophrenic patients].
    Shalimov VF
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1972; 72(2):268-76. PubMed ID: 5019828
    [No Abstract]   [Full Text] [Related]  

  • 2. [Final results of a clinical, genetic and cytogenetic study of 182 oligophrenic patients in a medico-educational institution. 1].
    Klein D; Marcoz JP; Mounoud RL; Bettschart W
    Schweiz Rundsch Med Prax; 1982 Jul; 71(28):1150-7. PubMed ID: 7122413
    [No Abstract]   [Full Text] [Related]  

  • 3. [A rare "cheerful" oligophrenic syndrome].
    Batenburg-Plenter AM
    Ned Tijdschr Geneeskd; 1976 Sep; 120(36):1528-30. PubMed ID: 967292
    [No Abstract]   [Full Text] [Related]  

  • 4. Diagnostic approach to a child with mental retardation.
    Pai GS
    Indian Pediatr; 1994 Jul; 31(7):879-90. PubMed ID: 7890364
    [No Abstract]   [Full Text] [Related]  

  • 5. Mental retardation in a family with phenylketonuria and mild hyperphenylalaninemia.
    Cohen BE; Szeinberg A; Berman W; Aviad Y; Crispin M; Hirshorn N; Goland R
    Pediatrics; 1969 Nov; 44(5):655-60. PubMed ID: 5374976
    [No Abstract]   [Full Text] [Related]  

  • 6. [Familial study of patients with psychosis, epilepsy and mental retardation].
    Liu XH
    Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1983 Apr; 16(2):99-102. PubMed ID: 6617371
    [No Abstract]   [Full Text] [Related]  

  • 7. [Dermatoglyphic changes in the palms of children with mental retardation of unknown etiology].
    Dabkowska M
    Psychiatr Pol; 1980; 14(3):277-82. PubMed ID: 7403369
    [No Abstract]   [Full Text] [Related]  

  • 8. The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation.
    Flint J; Wilkie AO; Buckle VJ; Winter RM; Holland AJ; McDermid HE
    Nat Genet; 1995 Feb; 9(2):132-40. PubMed ID: 7719339
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A family of progressive muscular dystrophy with mental retardation. Clinical observations.
    Suga M; Yoshimuta S; Hayashi Y; Sakamoto F
    Jinrui Idengaku Zasshi; 1966 Mar; 10(4):189-92. PubMed ID: 6008646
    [No Abstract]   [Full Text] [Related]  

  • 10. [Clinical, biological and genetic study of a family of phenylketonuric subjects].
    Pierson M; Frentz R; Marchal C; Thiriet M; Didier F; Humbel R
    Arch Fr Pediatr; 1968 Apr; 25(4):439-52. PubMed ID: 5671941
    [No Abstract]   [Full Text] [Related]  

  • 11. Research in mental retardation: toward an etiologic approach.
    Dykens EM; Hodapp RM
    J Child Psychol Psychiatry; 2001 Jan; 42(1):49-71. PubMed ID: 11205624
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A chromosomal survey of an institution for the mentally retarded. Study of 476 karyotypes with banding techniques and clinical assessment of patients with chromosome anomalies.
    Nielsen KB; Dyggve HV; Knudsen H; Olsen J
    Dan Med Bull; 1983 Feb; 30(1):5-13. PubMed ID: 6831943
    [No Abstract]   [Full Text] [Related]  

  • 13. [Epileptic syndrome associated with mental retardation].
    Timchev L; Petrova S
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1984; 84(6):847-9. PubMed ID: 6464603
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Subtelomeric rearrangements in mental retardation: Hacettepe University experience in 130 patients.
    Utine GE; Celik T; Alanay Y; Alikaşifoğlu M; Boduroğlu K; Tunçbilek E; Aktaş D
    Turk J Pediatr; 2009; 51(3):199-206. PubMed ID: 19817261
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Preventable fraction of mental retardation: analysis based on individuals with severe mental retardation.
    Stevenson RE; Massey PS; Schroer RJ; McDermott S; Richter B
    Ment Retard; 1996 Jun; 34(3):182-8. PubMed ID: 8684286
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Sex-related neurologic diseases. Familial X-linked mental retardation with a fragile X marker. Study of 8 families].
    Rodríguez Costa T; Gabarrón Llamas J; Casas Fernández C; Glover López G; Puche Mira A; Jiménez Cocina A
    An Esp Pediatr; 1984 Oct; 21 Suppl 20():54-7. PubMed ID: 6595955
    [No Abstract]   [Full Text] [Related]  

  • 17. [The frequency of some oligophrenias due to metabolic diseases in the grand-duchy of Luxembourg].
    Kutter D; Metz H
    Schweiz Arch Neurol Neurochir Psychiatr; 1968; 101(2):369-82. PubMed ID: 5705003
    [No Abstract]   [Full Text] [Related]  

  • 18. Ataxia-telangiectasia: a familial degenerative disease leading to mental retardation--a case report.
    Centerwall SA; Centerwall WR
    Am J Ment Defic; 1966 Sep; 71(2):185-90. PubMed ID: 5968852
    [No Abstract]   [Full Text] [Related]  

  • 19. Fragile X chromosome and X-linked mental retardation.
    Larbrisseau A; Jean P; Messier B; Richer CL
    Can Med Assoc J; 1982 Jul; 127(2):123-6. PubMed ID: 7093857
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Clinical and molecular screening for fragile X syndrome in 300 patients with non-specific mental retardation].
    Jara L; López M; Mellado C; Aspillaga M; Avendaño I; Blanco R
    Rev Med Chil; 1998 Aug; 126(8):911-8. PubMed ID: 9830742
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.