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 *

168 related articles for article (PubMed ID: 9206606)

  • 1. [The genetic diagnosis of children with mental retardation].
    Dunoyer-Mejía C
    Rev Neurol; 1997 May; 25(141):759-64. PubMed ID: 9206606
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Chromosomal anomalies in children with undifferentiated forms of metal retardation based on molecular cytogenetic research data].
    Vorsanova SG; Iurov IuB; Demidova IA; Vekhova NV
    Tsitol Genet; 1993; 27(3):72-8. PubMed ID: 8154052
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.
    Caliskan MO; Karauzum SB; Mihci E; Tacoy S; Luleci G
    Genet Couns; 2005; 16(2):129-38. PubMed ID: 16080292
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [The application and significance in prenatal diagnosis using G-banding, fluorescence in situ hybridization and comparative genomic hybridization].
    Zhang WS; Chen QN; Wu XH; Liang QH
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Apr; 26(2):156-60. PubMed ID: 19350506
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prevention of mental retardation: the role of medicine.
    Sells CJ; Bennett FC
    Am J Ment Defic; 1977 Sep; 82(2):117-29. PubMed ID: 71859
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Construction and application of the chromosomal specific probe pool from human chromosome no. 7].
    Xia JH; Du J; Dai HP; Fu JJ; Pan Q; Long ZG; Yuan QG; Li LY
    Shi Yan Sheng Wu Xue Bao; 1994 Sep; 27(3):321-9. PubMed ID: 7801726
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cytogenetic and fragile X molecular testing of individuals with mental retardation of unknown etiology.
    Patsalis PC; Sismani C; Hadjimarcou MI; Rose N; Stylianidou G; Koukoulli R; Anastasiadou V; Deltas CC; Middleton L
    Genet Couns; 1997; 8(1):1-6. PubMed ID: 9101271
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prenatal diagnosis of inherited satellited non-acrocentric chromosomes.
    Chen CP; Devriendt K; Chern SR; Lee CC; Wang W; Lin SP
    Prenat Diagn; 2000 May; 20(5):384-9. PubMed ID: 10820405
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [The impact of prenatal diagnosis on the prevention of chromosomal mental retardation. Chromosomal alterations that can be detected by prenatal diagnosis].
    Soler-Casas A; Sánchez-Díaz A; Morales-Peydró C
    Rev Neurol; 2006 Jan; 42 Suppl 1():S27-32. PubMed ID: 16506129
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Advances in molecular cytogenetics for the evaluation of mental retardation.
    Xu J; Chen Z
    Am J Med Genet C Semin Med Genet; 2003 Feb; 117C(1):15-24. PubMed ID: 12561054
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetics and educational psychology.
    Plomin R; Walker SO
    Br J Educ Psychol; 2003 Mar; 73(Pt 1):3-14. PubMed ID: 12639274
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Genetic causes of mental retardation--diagnostic possibilities].
    Tranebjaerg L
    Tidsskr Nor Laegeforen; 1999 Aug; 119(20):3028-34. PubMed ID: 10504854
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH).
    Kolialexi A; Kitsiou S; Fryssira H; Sofocleous C; Kouvidi E; Tsangaris GT; Salavoura K; Mavrou A
    In Vivo; 2006; 20(4):473-8. PubMed ID: 16900777
    [TBL] [Abstract][Full Text] [Related]  

  • 14. De novo complex chromosome rearrangement: a study of two patients.
    Melo DG; Huber J; Giuliani LR; Mazzucatto LF; Riegel M; Pina-Neto JM
    Genet Couns; 2004; 15(3):303-10. PubMed ID: 15517822
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic screening for mental retardation in Michigan.
    Thoene J; Higgins J; Krieger I; Schmickel R; Weiss L
    Am J Ment Defic; 1981 Jan; 85(4):335-40. PubMed ID: 7457497
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Characterization of a de novo balanced translocation in a patient with moderate mental retardation and dysmorphic features.
    Haddad MR; Mignon-Ravix C; Cacciagli P; Mégarbané A; Villard L
    Eur J Med Genet; 2009; 52(4):211-7. PubMed ID: 19379847
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Genetics of mental retardation].
    Prieto García F
    Neurologia; 1998 May; 13(5):218-22. PubMed ID: 9646628
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Study of 30 patients with unexplained developmental delay and dysmorphic features or congenital abnormalities using conventional cytogenetics and multiplex FISH telomere (M-TEL) integrity assay.
    Popp S; Schulze B; Granzow M; Keller M; Holtgreve-Grez H; Schoell B; Brough M; Hager HD; Tariverdian G; Brown J; Kearney L; Jauch A
    Hum Genet; 2002 Jul; 111(1):31-9. PubMed ID: 12136233
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Mental retardation: genetic counseling and prenatal diagnosis].
    Engel E
    Rev Med Suisse Romande; 1981 May; 101(5):341-6. PubMed ID: 7291823
    [No Abstract]   [Full Text] [Related]  

  • 20. Cerebellar dysgenesis and mental retardation associated with a complex chromosome rearrangement.
    Maserati E; Verri A; Seghezzi L; Tupler R; Federico A; Tiepolo L; Maraschio P
    Ann Genet; 1999; 42(4):210-4. PubMed ID: 10674160
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.