Population data suggest that deletions of 1p36 are a relatively common chromosome abnormality

Author:

Heilstedt HA,Ballif BC,Howard LA,Kashork CD,Shaffer LG

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference44 articles.

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

2. The promise and pitfalls of telomere region-specific probes;Ballif;Am J Hum Genet,2000

3. Korenberg Chromosome 1p36 deletions: the clinical phenotype and molecular characterization of a common newly delineated syndrome;Shapira;Am J Hum Genet,1997

4. Screening for submicroscopic chromosome rearrangements in children with idiopathic mental retardation using microsatellite markers for the chromosome telomeres;Slavotinek;J Med Genet,1999

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