Exome sequencing overrides formal genetics: ASPM mutations in a case study of apparent X-linked microcephalic intellectual deficit

Detalles Bibliográficos
Autores principales: Ariani, F, Mari, F, Amitrano, S, Di Marco, C, Artuso, R, Scala, E, Meloni, I, Della Volpe, R, Rossi, A, Bokhoven, H, Renieri, A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2013
Materias:
Letters to the Editor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3648977/
https://www.ncbi.nlm.nih.gov/pubmed/22823409
http://dx.doi.org/10.1111/j.1399-0004.2012.01901.x
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author Ariani, F
Mari, F
Amitrano, S
Di Marco, C
Artuso, R
Scala, E
Meloni, I
Della Volpe, R
Rossi, A
Bokhoven, H
Renieri, A
author_facet Ariani, F
Mari, F
Amitrano, S
Di Marco, C
Artuso, R
Scala, E
Meloni, I
Della Volpe, R
Rossi, A
Bokhoven, H
Renieri, A
author_sort Ariani, F
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spelling pubmed-36489772013-05-09 Exome sequencing overrides formal genetics: ASPM mutations in a case study of apparent X-linked microcephalic intellectual deficit Ariani, F Mari, F Amitrano, S Di Marco, C Artuso, R Scala, E Meloni, I Della Volpe, R Rossi, A Bokhoven, H Renieri, A Clin Genet Letters to the Editor Blackwell Publishing Ltd 2013-03 2013-04-19 /pmc/articles/PMC3648977/ /pubmed/22823409 http://dx.doi.org/10.1111/j.1399-0004.2012.01901.x Text en © 2013 John Wiley & Sons A/S http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Letters to the Editor
Ariani, F
Mari, F
Amitrano, S
Di Marco, C
Artuso, R
Scala, E
Meloni, I
Della Volpe, R
Rossi, A
Bokhoven, H
Renieri, A
Exome sequencing overrides formal genetics: ASPM mutations in a case study of apparent X-linked microcephalic intellectual deficit
title Exome sequencing overrides formal genetics: ASPM mutations in a case study of apparent X-linked microcephalic intellectual deficit
title_full Exome sequencing overrides formal genetics: ASPM mutations in a case study of apparent X-linked microcephalic intellectual deficit
title_fullStr Exome sequencing overrides formal genetics: ASPM mutations in a case study of apparent X-linked microcephalic intellectual deficit
title_full_unstemmed Exome sequencing overrides formal genetics: ASPM mutations in a case study of apparent X-linked microcephalic intellectual deficit
title_short Exome sequencing overrides formal genetics: ASPM mutations in a case study of apparent X-linked microcephalic intellectual deficit
title_sort exome sequencing overrides formal genetics: aspm mutations in a case study of apparent x-linked microcephalic intellectual deficit
topic Letters to the Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3648977/
https://www.ncbi.nlm.nih.gov/pubmed/22823409
http://dx.doi.org/10.1111/j.1399-0004.2012.01901.x
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