Cite

1. Bradinova I, Shopova S, Simeonov E. Mental retardation in childhood: clinical and diagnostic profile in 100 children. Genet Couns. 2005; 16(3): 239-248.Search in Google Scholar

2. Shiue CN, Lin YH, Kuan LC, Lii LM, Tsai WH, Chen YJ, Lin SJ, Kuo PL. Cytogenetic surveillance of mentally-retarded school children in southern Taiwan. J Formos Med Assoc. 2004; 103(3): 218-224.Search in Google Scholar

3. van Karnebeek CD, Jansweijer MC, Leenders AG, Offringa M, Hennekam RC. Diagnostic investigations in individuals with mental retardation: a systematic literature review of their usefulness. Eur J Hum Genet. 2005; 13(1): 6-25.10.1038/sj.ejhg.520127915523501Search in Google Scholar

4. Li SY, Tsai CC, Chou MY, Lin JK. A cytogenetic study of mentally retarded school children in Taiwan with special reference to the fragile X chromosome. Hum Genet. 1988; 79(4): 292-296.Search in Google Scholar

5. Coco R, Penchaszadeh VB. Cytogenetic findings in 200 children with mental retardation and multiple congenital anomalies of unknown cause. Am J Med Genet. 1982; 12(2): 155-173.10.1002/ajmg.13201202067102722Search in Google Scholar

6. Schreppers-Tijdink GA, Curfs LM, Wiegers A, Kleczkowska A, Fryns JP. A systematic cytogenetic study of a population of 1170 mentally retarded and/or behaviourly disturbed patients including fragile X-screening. The Hondsberg experience. J Genet Hum. 1988; 36(5): 425-446.Search in Google Scholar

7. van Karnebeek CD, Koevoets C, Sluijter S, Bijlsma EK, Smeets DF, Redeker EJ, Hennekam RC, Hoovers JM. Prospective screening for subtelomeric rearrangements in children with mental retardation of unknown aetiology: the Amsterdam experience. J Med Genet. 2002; 39(8): 546-553.10.1136/jmg.39.8.546173520412161591Search in Google Scholar

8. Bocian E, Mazurczak T, Stańczak H. Cytogenetic studies in clinical diagnosis analysis of 1611 examination results. Przegl Lek. 1995; 52(1): 5-9.Search in Google Scholar

9. Butler MG, Singh DN. Clinical and cytogenetic survey of institutionalized mentally retarded patients with emphasis on the fragile-X syndrome. J Intellect Disabil Res. 1993; 37(Pt 2): 131-142.10.1111/j.1365-2788.1993.tb00580.x54634538481611Search in Google Scholar

10. Celep F, Sönmez FM, Karagüzel A. Chromosomal abnormalities in 457 Turkish patients with MCA/MR. Turk J Pediatr. 2006; 48(2): 130-134.Search in Google Scholar

11. Srsen S, Misovicová N, Srsnová K, Volna J. Chromosome aberrations in a group of mentally retarded persons. Cesk Psychiatr. 1989; 85(1): 9-16.Search in Google Scholar

12. Xu J, Chen Z. Advances in molecular cytogenetics for the evaluation of mental retardation. Am J Med Genet C Semin Med Genet. 2003; 117C: 15-24.10.1002/ajmg.c.1001612561054Search in Google Scholar

13. Gosden CM, Davidson C, Robertson M. Lymphocyte culture. In: Rooney DE, Czepulkowski BH, Eds. Human Cytogenetics: A Practical Approach, Vol. I: Constitutional Analysis. Oxford: IRL Press Ltd. 1992: 31-54.Search in Google Scholar

14. Benn PA, Perle MA. Chromosome staining and banding techniques. In: Rooney DE, Czepulkowski BH, Eds. Human Cytogenetics: A Practical Approach, Vol. I: Constitutional Analysis. Oxford: IRL Press Ltd. 1992: 91-118.Search in Google Scholar

15. Liehr T, Weise A. Frequency of small supernumerary marker chromosomes in prenatal, newborn, developmentally retarded and infertility diagnostics. Int J Mol Med. 2007; 19(5): 719-731.10.3892/ijmm.19.5.719Search in Google Scholar

16. Mowat DR, Croaker GDH, Cass DT, Kerr BA, Chaitow J, Ades LC, Chia NL, Wilson MJ. Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23. J Med Genet. 1998; 35(8): 617-623.10.1136/jmg.35.8.61710513839719364Search in Google Scholar

17. Wu X, Rush JS, Karaoglu D, Krasnewich D, Lubinsky MS, Waechter CJ, Gilmore R, Freeze HH. Deficiency of UDP-GlcNAc:dolichol phosphate N-acetylgluco-samine-1 phosphate transferase (DPAGT1) causes a novel congenital disorder of glycosylation type II. Hum Mutat. 2003; 22(2): 144-150.10.1002/humu.1023912872255Search in Google Scholar

18. Kriek M, White SJ, Bouma MC, Dauwerse HG, Hansson KB, Nijhuis JV, Bakker B, van Ommen GJ, den Dunnen JT, Breuning MH. Genomic imbalances in mental retardation. J Med Genet. 2004; 43(4): 362-370.10.1136/jmg.2003.014308173574815060096Search in Google Scholar

ISSN:
1311-0160
Language:
English
Publication timeframe:
2 times per year
Journal Subjects:
Medicine, Basic Medical Science, other