Use of fluorescence in situ hybridization to clarify a complex chromosomal rearrangement in a child with multiple congenital anomalies
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference13 articles.
1. Comparison of high resolution chromosome banding and fluorescence in situ hybridization (FISH) for the laboratory evaluation of Prader-Willi syndrome and angelman syndrome
2. (1985): “ISCN 1985; An International System for Human Cytogenetic Nomenclature (1985).” Switzerland: S. Karger Medical and Scientific Publishers.
3. Complex chromosomal rearrangement in a woman with multiple miscarriages
4. Fluorescent In Situ Hybridization: Use of Whole Chromosome Paint Probes to Identify Unbalanced Chromosome Translocations
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