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 *

236 related articles for article (PubMed ID: 17111918)

  • 1. [The use of modern diagnostic and preventive technologies in children with hereditary and congenital intellectual developmental disorders].
    Vel'tishchev IuE; Tsaregorodtsev AD; Novikov PV; Vorsanova SG
    Vestn Ross Akad Med Nauk; 2006; (9-10):11-8. PubMed ID: 17111918
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Assessment unit for the mentally retarded.
    Jancar J
    Bristol Med Chir J; 1971 Apr; 86(318):27-32. PubMed ID: 4257179
    [No Abstract]   [Full Text] [Related]  

  • 3. Confirmation of chromosomal microarray as a first-tier clinical diagnostic test for individuals with developmental delay, intellectual disability, autism spectrum disorders and dysmorphic features.
    Battaglia A; Doccini V; Bernardini L; Novelli A; Loddo S; Capalbo A; Filippi T; Carey JC
    Eur J Paediatr Neurol; 2013 Nov; 17(6):589-99. PubMed ID: 23711909
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Congenital hypothyroidism].
    Szymborska M
    Med Wieku Rozwoj; 2000; 4(4):451-65. PubMed ID: 11228603
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mental retardation.
    Palmer FB; Capute AJ
    Pediatr Rev; 1994 Dec; 15(12):473-9. PubMed ID: 7845869
    [No Abstract]   [Full Text] [Related]  

  • 6. Genetic diagnostic studies for mental retardation.
    Beaudet AL
    Curr Probl Pediatr; 1978 Mar; 8(5):1-47. PubMed ID: 657833
    [No Abstract]   [Full Text] [Related]  

  • 7. Intellectual outcomes of patients with congenital hypothyroidism not detected by neonatal screening.
    Hsiao PH; Chiu YN; Tsai WY; Su SC; Lee JS; Soong WT
    J Formos Med Assoc; 1999 Jul; 98(7):512-5. PubMed ID: 10463002
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Multiplex Ligation - dependent Probe Amplification (MLPA) as a screening test in children with developmental defects and intellectual disability of unknown etiology].
    Laczmańska I; Jakubiak A; Slęzak R; Pesz K; Stembalska A; Laczmański L; Sąsiadek MM; Smigiel R
    Med Wieku Rozwoj; 2011; 15(2):132-9. PubMed ID: 22002044
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Various medico-social aspects of children's disability in the Kirghiz SSR].
    Zoletilo AI; Koĭkelov SD
    Sov Zdravookhr; 1990; (6):33-5. PubMed ID: 2145634
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Genetic causes of mental retardation].
    Rehder H; Fritz B
    Wien Med Wochenschr; 2005 Jun; 155(11-12):258-67. PubMed ID: 16035386
    [TBL] [Abstract][Full Text] [Related]  

  • 11. On the diagnosis of syndromes in mental retardation.
    Garrard SD
    Pediatr Clin North Am; 1968 Nov; 15(4):925-42. PubMed ID: 4236263
    [No Abstract]   [Full Text] [Related]  

  • 12. 6p subtelomere deletion with congenital glaucoma, severe mental retardation, and growth impairment.
    Nakane T; Kousuke N; Sonoko H; Yuko K; Sato H; Kubota T; Sugita K
    Pediatr Int; 2013 Jun; 55(3):376-81. PubMed ID: 23782370
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Etiologic and pathogenetic study of mental retardation with multiple congenital anomalies.
    Ohdo S; Sonoda T; Ohba K; Hayakawa K
    Acta Paediatr Jpn; 1992 Apr; 34(2):144-50. PubMed ID: 1377860
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Effect of expanded newborn screening for biochemical genetic disorders on child outcomes and parental stress.
    Waisbren SE; Albers S; Amato S; Ampola M; Brewster TG; Demmer L; Eaton RB; Greenstein R; Korson M; Larson C; Marsden D; Msall M; Naylor EW; Pueschel S; Seashore M; Shih VE; Levy HL
    JAMA; 2003 Nov; 290(19):2564-72. PubMed ID: 14625333
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Applied biomedical research in mental retardation--prevention.
    Coons CE; Frankenburg WK
    Appl Res Ment Retard; 1982; 3(3):221-31. PubMed ID: 6184016
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Effects of neonatal screening for hypothyroidism: prevention of mental retardation by treatment before clinical manifestations. New England congenital hypothyroidism collaborative.
    Lancet; 1981 Nov; 2(8255):1095-8. PubMed ID: 6118534
    [No Abstract]   [Full Text] [Related]  

  • 17. [The abnormality-retardation syndrome].
    Neuhäuser G
    Monatsschr Kinderheilkd (1902); 1978 May; 126(5):259-63. PubMed ID: 651909
    [No Abstract]   [Full Text] [Related]  

  • 18. Correlation between euploid structural chromosome rearrangements and mental subnormality in humans.
    Jacobs PA
    Nature; 1974 May; 249(453):164-5. PubMed ID: 4275486
    [No Abstract]   [Full Text] [Related]  

  • 19. An aetiological study of 1,000 patients with an I.Q. assessment below 51.
    Turner G
    Med J Aust; 1975 Dec 20-27; 2(25-26):927-31. PubMed ID: 130531
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [A model for clinical diagnosis-treatment of the newborn with an abnormal screening test for hypothyroidism and in children with congenital hypothyroidism].
    Szymborska M
    Med Wieku Rozwoj; 2000; 4(4):467-74. PubMed ID: 11228604
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.