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 *

143 related articles for article (PubMed ID: 3392842)

  • 1. Chromosome abnormalities and epileptic seizures.
    Ieshima A; Takeshita K
    Jinrui Idengaku Zasshi; 1988 Mar; 33(1):49-60. PubMed ID: 3392842
    [No Abstract]   [Full Text] [Related]  

  • 2. Two cases with a ring chromosome in group E.
    Aula P; Gripenberg U; Hjelt L; Kivalo E; Leisti J; Palo J; von Schoultz B; Suomalainen E
    Acta Neurol Scand; 1967; 43(S31):51-2. PubMed ID: 5583277
    [No Abstract]   [Full Text] [Related]  

  • 3. [Coexistence of Sjogren-Larsson syndrome and Rud's syndrome in the same family].
    Kissel P; André JM; André M
    J Genet Hum; 1973 Mar; 21(1):15-22. PubMed ID: 4742119
    [No Abstract]   [Full Text] [Related]  

  • 4. [2 new cases of ring chromosome 14].
    Caille B; Rethoré MO; Raoul O; Huet de Barochez Y; Dufier JL; Roy C; Harpey JP; Valdes L; Noseda J
    Ann Pediatr (Paris); 1985 May; 32(5):441-6. PubMed ID: 4026139
    [No Abstract]   [Full Text] [Related]  

  • 5. Studies on chromosomal anomaly syndrome with epilepsy.
    Sugama S; Akatsuka A; Ochiai Y; Tsuzura S; Maekawa K
    Jpn J Psychiatry Neurol; 1993 Jun; 47(2):283-5. PubMed ID: 8271565
    [No Abstract]   [Full Text] [Related]  

  • 6. [Causes of mental retardation in childhood (analysis of 414 cases)].
    Hanefeld F; König E
    Monatsschr Kinderheilkd (1902); 1974 Jul; 122(7):679-80. PubMed ID: 4471761
    [No Abstract]   [Full Text] [Related]  

  • 7. [Agenesis of the corpus callosum and epilepsy. 26 cases].
    Septien L; Gras P; Giroud M; Martin D; Binnert D; Dumas R
    Rev Neurol (Paris); 1993; 149(4):257-61. PubMed ID: 8235222
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The genetics of epilepsy.
    Anderson VE; Hauser WA
    Prog Med Genet; 1985; 6():9-52. PubMed ID: 3915368
    [No Abstract]   [Full Text] [Related]  

  • 9. [Epilepsy in chromosome aberrations].
    Bahi-Buisson N; Ville D; Eisermann M; Plouin P; Kaminska A; Chiron C
    Arch Pediatr; 2005 Apr; 12(4):449-58. PubMed ID: 15808438
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The results of chromosome examinations in an institution for mental retardates in the Cape Province.
    Nelson MM; Smart RD
    S Afr Med J; 1982 Jul; 62(1):25-9. PubMed ID: 7089776
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mental deficiency and malformations in a boy with a group-C ring chromosome: 46, XY, Cr.
    Wurster D; Pomeroy J; Benirschke K; Hoefnagel D
    J Ment Defic Res; 1969 Sep; 13(3):184-90. PubMed ID: 5823674
    [No Abstract]   [Full Text] [Related]  

  • 12. Chromosomal microarray analysis of Bulgarian patients with epilepsy and intellectual disability.
    Peycheva V; Kamenarova K; Ivanova N; Stamatov D; Avdjieva-Tzavella D; Alexandrova I; Zhelyazkova S; Pacheva I; Dimova P; Ivanov I; Litvinenko I; Bozhinova V; Tournev I; Simeonov E; Mitev V; Jordanova A; Kaneva R
    Gene; 2018 Aug; 667():45-55. PubMed ID: 29753047
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prevention of retardation of genetic origin.
    Holtzman NA
    Pediatr Clin North Am; 1973 Feb; 20(1):151-8. PubMed ID: 4577325
    [No Abstract]   [Full Text] [Related]  

  • 14. The causes of severe mental handicap.
    Mackay RI
    Dev Med Child Neurol; 1982 Jun; 24(3):386-8. PubMed ID: 7095307
    [No Abstract]   [Full Text] [Related]  

  • 15. Agenesis of corpus callosum: clinical description and etiology.
    Marszał E; Jamroz E; Pilch J; Kluczewska E; Jabłecka-Deja H; Krawczyk R
    J Child Neurol; 2000 Jun; 15(6):401-5. PubMed ID: 10868784
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Epilepsy.
    Friedlander WJ
    Prog Neurol Psychiatry; 1968; 23():203-41. PubMed ID: 4388825
    [No Abstract]   [Full Text] [Related]  

  • 17. Ring chromosome 14 in a mentally retarded girl.
    Iselius L; Ritzén M; Bui TH; Olsson K; Eklöf O
    Acta Paediatr Scand; 1980 Nov; 69(6):803-6. PubMed ID: 7211367
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Additional small acrocentric chromosome: two cases.
    Nielsen J; Tsuboi T; Friedrich U; Mikkelsen M; Lund B; Steinicke O
    J Ment Defic Res; 1969 Jun; 13(2):106-22. PubMed ID: 5794285
    [No Abstract]   [Full Text] [Related]  

  • 19. Chromosomal microaberrations in patients with epilepsy, intellectual disability, and congenital anomalies.
    Spreiz A; Haberlandt E; Baumann M; Baumgartner Sigl S; Fauth C; Gautsch K; Karall D; Janetschek C; Rostasy K; Scholl-Bürgi S; Zotter S; Utermann G; Zschocke J; Kotzot D
    Clin Genet; 2014 Oct; 86(4):361-6. PubMed ID: 24116836
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Human chromosome hot points. 1. Hot point at 3p14 in three populations.
    Zhou XT; Xu BH; Chu CL; Xia GF; Li N; Sha R
    Hum Genet; 1984; 67(3):249-51. PubMed ID: 6469239
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.