Literature DB >> 15603454

The use of subtelomeric probes to study mental retardation.

Samantha J L Knight1, Jonathan Flint.   

Abstract

In this chapter, we focus on the genetic basis of mental retardation (MR), specifically the use of subtelomeric probes to provide new diagnoses in idiopathic MR. We discuss both the background to the clinical demand for diagnoses and the technological advances that culminated in the development of subtelomeric testing strategies. We explain the theory behind these strategies and briefly outline the protocols involved, giving the advantages, limitations, and pitfalls of the analyses. Finally, we give an overview of the MR subtelomeric studies to date and how subtelomeric testing has become a widely used tool in clinical diagnostic laboratories, particularly in the diagnosis of unexplained MR, but also in other fields of clinical medicine. The conclusion addresses the overall impact that subtelomeric testing has had on the diagnosis of MR, the implications for patients and their families, and future research avenues for exploring the genetic causes of MR and improving our overall understanding of neurocognitive development.

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Year:  2004        PMID: 15603454     DOI: 10.1016/s0091-679x(04)75035-9

Source DB:  PubMed          Journal:  Methods Cell Biol        ISSN: 0091-679X            Impact factor:   1.441


  5 in total

1.  Prenatal diagnosis of genomic disorders and chromosome abnormalities using array-based comparative genomic hybridization.

Authors:  Francesca Gullotta; Michela Biancolella; Elena Costa; Isabella Colapietro; Anna Maria Nardone; Paolo Molinaro; Adalgisa Pietropolli; Marianovella Narcisi; Cristiana Di Rosa; Giuseppe Novelli
Journal:  J Prenat Med       Date:  2007-01

Review 2.  Microarray-Based Comparative Genomic Hybridization, Multiplex Ligation-Dependent Probe Amplification, and High-Resolution Karyotype for Differential Diagnosis Oculoauriculovertebral Spectrum: A Systematic Review.

Authors:  Andressa Barreto Glaeser; Bruna Lixinski Diniz; Desirée Deconte; Andressa Schneiders Santos; Rafael Fabiano Machado Rosa; Paulo Ricardo Gazzola Zen
Journal:  J Pediatr Genet       Date:  2020-05-27

Review 3.  From microscopes to microarrays: dissecting recurrent chromosomal rearrangements.

Authors:  Beverly S Emanuel; Sulagna C Saitta
Journal:  Nat Rev Genet       Date:  2007-11       Impact factor: 53.242

4.  Human subtelomeres are hot spots of interchromosomal recombination and segmental duplication.

Authors:  Elena V Linardopoulou; Eleanor M Williams; Yuxin Fan; Cynthia Friedman; Janet M Young; Barbara J Trask
Journal:  Nature       Date:  2005-09-01       Impact factor: 49.962

5.  Identification of a recurrent breakpoint within the SHANK3 gene in the 22q13.3 deletion syndrome.

Authors:  M C Bonaglia; R Giorda; E Mani; G Aceti; B-M Anderlid; A Baroncini; T Pramparo; O Zuffardi
Journal:  J Med Genet       Date:  2005-11-11       Impact factor: 6.318

  5 in total

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