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Trisomy 3q25.1-qter and monosomy 8p23.1-pter in a patient: Cytogenetic and molecular analysis with delineation of the phenotype

✍ Scribed by G. Zafra de la Rosa; C.A. Venegas-Vega; N. Monroy; G. Contreras-Bucio; U. Friedrich; M. Houman; A. Saad; P. Fernández; S. Kofman-Alfaro; A. Cervantes

Publisher
John Wiley and Sons
Year
2005
Tongue
English
Weight
173 KB
Volume
136A
Category
Article
ISSN
1552-4825

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## Abstract We report on a clinical and molecular cytogenetic study of a patient who presents a complex chromosomal rearrangement with two different cell lines. Using high‐resolution GTG banding and fluorescence in situ hybridization (FISH) with several probes, including bacterial artificial chromo