Genotyping FOXG1 Mutations in Patients With Clinical Evidence of the FOXG1 Syndrome

Molecular Syndromology - Switzerland
doi 10.1159/000345845
Full Text
Abstract

Available in full text

Categories
Genetics
Date
Authors
Publisher

S. Karger AG

Related search

FOXG1 Dose in Brain Development

Frontiers in Pediatrics
Child HealthPediatricsPerinatology
2019English

Platelet Defects in Congenital Variant of Rett Syndrome Patients With FOXG1 Mutations or Reduced Expression Due to a Position Effect at 14q12

European Journal of Human Genetics
Genetics
2013English

Visual Impairment in FOXG1-mutated Individuals and Mice

Neuroscience
Neuroscience
2016English

FOXG1 Orchestrates Neocortical Organization and Cortico-Cortical Connections

Neuron
Neuroscience
2018English

Partial Monosomy14q Involving FOXG1 and NOVA1 in an Infant With Microcephaly, Seizures and Severe Developmental Delay

Molecular Cytogenetics
BiochemistryMolecular MedicineGeneticsMolecular Biology
2016English

Deep Genotyping of the IDS Gene in Colombian Patients With Hunter Syndrome

JIMD Reports
Internal MedicineGeneticsMolecular BiologyBiochemistryEndocrinologyMetabolismDiabetes
2014English

The Transcription Factor Foxg1 Regulates Telencephalic Progenitor Proliferation Cell Autonomously, in Part by Controlling Pax6 Expression Levels

Neural Development
Developmental Neuroscience
2011English

MicroRNA-9 Modulates Cajal-Retzius Cell Differentiation by Suppressing Foxg1 Expression in Mouse Medial Pallium

Journal of Neuroscience
Neuroscience
2008English

Mutations inRIT1cause Noonan Syndrome - Additional Functional Evidence and Expanding the Clinical Phenotype

Clinical Genetics
Genetics
2015English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy