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Publication details

Document type
Journal articles

Document subtype
Abstract

Title
Increased frequency of the autism broader phenotype in mothers transmitting etiological CNVs to sons affected by Autism Spectrum Disorder (ASD)

Participants in the publication
M. Asif (Author)
I. Conceição (Author)
K. Kwiatkowska (Author)
C. Rasga (Author)
C. Café (Author)
L. Sousa (Author)
Dep. Estatística e Investigação Operacional
 CEAUL
 G. Oliveira (Author)
F. Couto (Author)
Dep. Informática
 LASIGE
 A. Vicente (Author)

Date of Publication
2016-05

Where published
European Journal of Human Genetics

Publication Identifiers
ISSN - 10184813

Organizers
European Human Genetics Conference (ESHG)

Publisher
Nature Publishing Group

Volume
24
Number
E-Suppl 1

Starting page
184
Last page
184

Document Identifiers
URL - https://www.eshg.org/fileadmin/www.eshg.org/conferences/2016/downloads/ESHG2016_Abstracts_final.pdf

Rankings
SCIMAGO Q1 (2016) - 2.092 - Medicine Genetics (clinical)


Export

APA
M. Asif, I. Conceição, K. Kwiatkowska, C. Rasga, C. Café, L. Sousa, G. Oliveira, F. Couto, A. Vicente, (2016). Increased frequency of the autism broader phenotype in mothers transmitting etiological CNVs to sons affected by Autism Spectrum Disorder (ASD). European Journal of Human Genetics, 24, 184-184. ISSN 10184813. eISSN . https://www.eshg.org/fileadmin/www.eshg.org/conferences/2016/downloads/ESHG2016_Abstracts_final.pdf

IEEE
M. Asif, I. Conceição, K. Kwiatkowska, C. Rasga, C. Café, L. Sousa, G. Oliveira, F. Couto, A. Vicente, "Increased frequency of the autism broader phenotype in mothers transmitting etiological CNVs to sons affected by Autism Spectrum Disorder (ASD)" in European Journal of Human Genetics, vol. 24, pp. 184-184, 2016.

BIBTEX
@article{40166, author = {M. Asif and I. Conceição and K. Kwiatkowska and C. Rasga and C. Café and L. Sousa and G. Oliveira and F. Couto and A. Vicente}, title = {Increased frequency of the autism broader phenotype in mothers transmitting etiological CNVs to sons affected by Autism Spectrum Disorder (ASD)}, journal = {European Journal of Human Genetics}, year = 2016, pages = {184-184}, volume = 24 }