Go to:
Logótipo
Você está em: Start > Publications > View > Intragenic Deletions in NRXN1: Insights from aCGH Analysis in Neurodevelopmental Disorders
Map of Premises
Principal
Publication

Intragenic Deletions in NRXN1: Insights from aCGH Analysis in Neurodevelopmental Disorders

Title
Intragenic Deletions in NRXN1: Insights from aCGH Analysis in Neurodevelopmental Disorders
Type
Another Publication in an International Scientific Journal
Year
2024
Authors
doria, s
(Author)
FMUP
View Personal Page You do not have permissions to view the institutional email. Search for Participant Publications View Authenticus page View ORCID page
Pinto, J
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. Without AUTHENTICUS Without ORCID
Almeida, C
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. Without AUTHENTICUS Without ORCID
Pinho, MJ
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. Without AUTHENTICUS Without ORCID
Santos, MH
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. Without AUTHENTICUS Without ORCID
Grangeia, A
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. Without AUTHENTICUS Without ORCID
Journal
Pages: 1584-1585
ISSN: 1018-4813
Publisher: Springer Nature
Indexing
Publicação em ISI Web of Knowledge ISI Web of Knowledge - 0 Citations
Other information
Authenticus ID: P-018-DFV
Resumo (PT):
Abstract (EN):
Language: English
Type (Professor's evaluation): Scientific
Documents
We could not find any documents associated to the publication.
Related Publications

Of the same journal

Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases (2021)
Another Publication in an International Scientific Journal
Zurek, B; Ellwanger, K; Vissers, LELM; Schüle, R; Synofzik, M; Töpf, A; de Voer, RM; Laurie, S; Matalonga, L; Gilissen, C; Ossowski, S; ¿t Hoen, PAC; Vitobello, A; Schulze Hentrich, JM; Riess, O; Brunner, HG; Brookes, AJ; Rath, A; Bonne, G; Gumus, G...(mais 203 authors)
On two Jewish clades in mitochondrial DNA Reply (2015)
Another Publication in an International Scientific Journal
Ines Nogueiro; Joao Teixeira; Antonio Amorim; Leonor Gusmao; Luis Alvarez
Improving the in silico assessment of pathogenicity for compensated variants (2017)
Another Publication in an International Scientific Journal
Luisa Azevedo; Mort, M; Costa, AC; Silva, RM; Quelhas, D; Amorim, A; Cooper, DN
Impact of recurrent 17q12 microdeletion across three generations: a family with complete penetrance (2024)
Another Publication in an International Scientific Journal
Beleza, I; Vilan, A; doria, s; Grangeia, A
Hao-Fountain Syndrome: first reports of inherited variants (2024)
Another Publication in an International Scientific Journal
da Rocha, DF; Santos, V; doria, s; Grangeia, A

See all (45)

Recommend this page Top
Copyright 1996-2025 © Faculdade de Medicina Dentária da Universidade do Porto  I Terms and Conditions  I Acessibility  I Index A-Z
Page created on: 2025-11-05 at 03:35:41 | Privacy Policy | Personal Data Protection Policy | Whistleblowing | Electronic Yellow Book