Interstitial deletion 15q21 and Prader-Willi like syndrome phenotype: Case report

Introduction: Chromosome 15q interstitial deletions not involving the Prader-Willi/Angelman region are uncommon and poorly characterized. Very few cases of different segmental losses involving the 15q21 region have been reported at cytogenetic level. All the described patients present with moderate...

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Bibliographic Details
Main Author: Pires, S. (author)
Other Authors: Oliva Teles, N. (author), Ribeiro, J. (author), Mota Freitas, M. (author), Marques, B. (author), Reis, G. (author), Correia, H. (author), Fonseca e Silva, M.L. (author)
Format: conferenceObject
Language:eng
Published: 2013
Subjects:
Doenças Genéticas
Interstitial Deletion
Prader-Willi Syndrome
Online Access:http://hdl.handle.net/10400.18/1219
Country:Portugal
Oai:oai:repositorio.insa.pt:10400.18/1219

Internet

http://hdl.handle.net/10400.18/1219

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