Recombinants of intrachromosomal transposition of subtelomeres in chromosomes 1 and 2: A cause of minute terminal chromosomal imbalances

Author:

Daniel Art,Baker Elizabeth,Chia Nicole,Haan Eric,Malafiej Paul,Hinton Lyn,Clarke Nigel,Adès Lesley,Darmanian Artur,Callen David

Funder

WCH Foundation

APEX Foundation

Wellcome Trust

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference33 articles.

1. A study of 250 children with idiopathic mental retardation reveals nine cryptic and diverse telomeric chromosome anomalies;Baker;Am J Med Genet,2002

2. Fishing for mechanisms of cytogenetically defined terminal deletions using chromosome-specific subtelomeric probes;Ballif;Eur J Hum Genet,2000

3. Familial cryptic translocation between chromosomes 2qter and 8qter: further delineation of the Albright hereditary osteodystrophy-like phenotype;Bijlsma;J Med Genet,1999

4. An infant with karyotype 46,XX,del(2)(q37) and severe congenital abnormalities;Coldwell;Am J Hum Genet,1992

5. The plasticity of human telomeres demonstrated by a hypervariable telomere repeat array that is located on some copies of 16p and 16q;Coleman;Hum Mol Genet,1999

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