Contains fulltext : 150754.pdf (publisher's version ) (Closed access
Mutations in FOXP1, located at 3p13, have been reported in patients with global developmental delay ...
Abstract Background Haploinsufficiency of the forkhead-box protein P1 (FOXP1) gene leads to a neurod...
Contains fulltext : 165642.pdf (publisher's version ) (Open Access)20 p
The FOXP subfamily includes four different transcription factors: FOXP1, FOXP2, FOXP3, and FOXP4, al...
Background: Mutations in forkhead box protein P1 (FOXP1) cause intellectual disability (ID) and spec...
Mutations in forkhead box protein P1 (FOXP1) cause intellectual disability (ID) and specific languag...
BACKGROUND: Mutations in forkhead box protein P1 (FOXP1) cause intellectual disability (ID) and spec...
FOXP1 (forkhead box protein P1) is a transcription factor involved in the development of several tis...
Heterozygous variants disrupting the FOXP1 transcription factor (forkhead box protein P1; OMIM 60551...
De novo disruptions of the neural transcription factor FOXP1 are a recently discovered, rare cause o...
Intellectual disability (ID) is a neurodevelopmental disorder manifesting in children before the age...
ObjectiveWe aimed to report on previously unappreciated clinical features associated with FOXP1-rela...
ObjectiveWe aimed to report on previously unappreciated clinical features associated with FOXP1-rela...
Heterozygous mutations in FOXP2, which encodes a forkhead transcription factor, have been shown to c...
ObjectiveWe aimed to report on previously unappreciated clinical features associated with FOXP1-rela...
Mutations in FOXP1, located at 3p13, have been reported in patients with global developmental delay ...
Abstract Background Haploinsufficiency of the forkhead-box protein P1 (FOXP1) gene leads to a neurod...
Contains fulltext : 165642.pdf (publisher's version ) (Open Access)20 p
The FOXP subfamily includes four different transcription factors: FOXP1, FOXP2, FOXP3, and FOXP4, al...
Background: Mutations in forkhead box protein P1 (FOXP1) cause intellectual disability (ID) and spec...
Mutations in forkhead box protein P1 (FOXP1) cause intellectual disability (ID) and specific languag...
BACKGROUND: Mutations in forkhead box protein P1 (FOXP1) cause intellectual disability (ID) and spec...
FOXP1 (forkhead box protein P1) is a transcription factor involved in the development of several tis...
Heterozygous variants disrupting the FOXP1 transcription factor (forkhead box protein P1; OMIM 60551...
De novo disruptions of the neural transcription factor FOXP1 are a recently discovered, rare cause o...
Intellectual disability (ID) is a neurodevelopmental disorder manifesting in children before the age...
ObjectiveWe aimed to report on previously unappreciated clinical features associated with FOXP1-rela...
ObjectiveWe aimed to report on previously unappreciated clinical features associated with FOXP1-rela...
Heterozygous mutations in FOXP2, which encodes a forkhead transcription factor, have been shown to c...
ObjectiveWe aimed to report on previously unappreciated clinical features associated with FOXP1-rela...
Mutations in FOXP1, located at 3p13, have been reported in patients with global developmental delay ...
Abstract Background Haploinsufficiency of the forkhead-box protein P1 (FOXP1) gene leads to a neurod...
Contains fulltext : 165642.pdf (publisher's version ) (Open Access)20 p
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