- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
Developmental disorders associated with PTEN gene: case series report ; volume:81 ; number:S 01 ; year:2023 ; 01
Konferenz: SBN Conference 2022; 2022-11-09; Expo United Curitiba
Arquivos de neuro-psiquiatria ; 81, Heft S 01 (2023), 01
- Contributor
-
Good, Gabrielle Gruppelli
Fatuch, Maria Vitória Ruiz
Précoma, Marina Massuchin
Cota, Ana Luiza de Rezende e.
Silva, Giulia Vilela
Valle, Daniel Almeida do
Gugelmin, Lucas Procopiak
Maldonado, Maria Fernanda Jara
Correa, Maria Vitória
- DOI
-
10.1055/s-0043-1774577
- URN
-
urn:nbn:de:101:1-2023110211284571430027
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:50 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Good, Gabrielle Gruppelli
- Fatuch, Maria Vitória Ruiz
- Précoma, Marina Massuchin
- Cota, Ana Luiza de Rezende e.
- Silva, Giulia Vilela
- Valle, Daniel Almeida do
- Gugelmin, Lucas Procopiak
- Maldonado, Maria Fernanda Jara
- Correa, Maria Vitória
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Current developmental disorders reports$pexi
Chromatin modifier developmental pluripotency associated factor 4 (DPPA4) is a candidate gene for alcohol-induced developmental disorders
“Thyroid nodular disease and PTEN mutation in a multicentre series of children with PTEN hamartoma tumor syndrome (PHTS)”
Cyclin-dependent kinases and rare developmental disorders
Review journal of autism and developmental disorders
Distinct epigenomic patterns are associated with haploinsufficiency and predict risk genes of developmental disorders
A novel missense PTEN mutation identified in a patient with macrocephaly and developmental delay
Down syndrome and related developmental disorders : 5 tables
Understanding Typing Skill in Students With Developmental Disorders
In frame exon skipping in UBE3B is associated with developmental disorders and increased mortality in cattle
Deletions in chromosome 6p22.3-p24.3, including ATXN1, are associated with developmental delay and autism spectrum disorders
Single-cell, whole-embryo phenotyping of mammalian developmental disorders
Current developmental disorders reports$pexi
Chromatin modifier developmental pluripotency associated factor 4 (DPPA4) is a candidate gene for alcohol-induced developmental disorders
“Thyroid nodular disease and PTEN mutation in a multicentre series of children with PTEN hamartoma tumor syndrome (PHTS)”
Cyclin-dependent kinases and rare developmental disorders
Review journal of autism and developmental disorders
Distinct epigenomic patterns are associated with haploinsufficiency and predict risk genes of developmental disorders
A novel missense PTEN mutation identified in a patient with macrocephaly and developmental delay
Down syndrome and related developmental disorders : 5 tables
Understanding Typing Skill in Students With Developmental Disorders
In frame exon skipping in UBE3B is associated with developmental disorders and increased mortality in cattle
Deletions in chromosome 6p22.3-p24.3, including ATXN1, are associated with developmental delay and autism spectrum disorders