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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Detalhes bibliográficos
Autor principal: Pires, S. (author)
Outros Autores: 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)
Formato: conferenceObject
Idioma:eng
Publicado em: 2013
Assuntos:
Texto completo:http://hdl.handle.net/10400.18/1219
País:Portugal
Oai:oai:repositorio.insa.pt:10400.18/1219