Characterization of terminal chromosome anomalies using multisubtelomere FISH
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference35 articles.
1. Subtelomeric rearrangements detected in patients with idiopathic mental retardation
2. FISHing for mechanisms of cytogenetically defined terminal deletions using chromosome-specific subtelomeric probes
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4. Inverted duplications are recurrent rearrangements always associated with a distal deletion: description of a new case involving 2q
5. dup(4p 15→4pter) in a 19-year-old woman resulting from a maternal 4;14 translocation
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2. Chromosomes and the Skin;Harper's Textbook of Pediatric Dermatology;2011-05-24
3. Detection of mosaicism for genome imbalance in a cohort of 3,042 clinical cases using an oligonucleotide array CGH platform;European Journal of Medical Genetics;2011-03
4. Prenatal Diagnosis of a Fetus with Terminal Deletion of Chromosome 1 (q43) in First-Trimester Screening: Is There a Characteristic Antenatal 1q Deletion Phenotype? A Case Report and Review of the Literature;Fetal Diagnosis and Therapy;2011
5. Detection of microchromosomal aberrations in refractory epilepsy: a pilot study;Epileptic Disorders;2010-09
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