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Partial deletion of chromosome 12q is not usually associated with CFC syndrome

✍ Scribed by Zollino, Marcella ;Neri, Giovanni


Publisher
John Wiley and Sons
Year
2000
Tongue
English
Weight
42 KB
Volume
95
Category
Article
ISSN
0148-7299

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## Abstract In the neurodevelopmentally impaired population the frequency of small supernumerary marker chromosomes (sSMC) is about 0.3%. To find the origin of a sSMC in a 4‐year‐old boy with Asperger syndrome (AS) a microarray‐based comparative genomic hybridization (aCGH), using a 135K‐feature wh