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Molecular cytogenetic characterization of a 10p14 deletion that includes the DGS2 region in a patient with multiple anomalies

✍ Scribed by Skrypnyk, Cristina ;Goecke, Timm O. ;Majewski, Frank ;Bartsch, Oliver


Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
225 KB
Volume
113
Category
Article
ISSN
0148-7299

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## Abstract Deletion 3p syndrome is associated with characteristic facial features, growth failure, and mental retardation. Typically, individuals with deletion 3p syndrome have terminal deletions that result in loss of material from 3p25 to 3pter. We present a child with a clinical phenotype consi