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Publications by D.W. Pratt

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

Molecular Syndromology

English

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FOXG1 Dose in Brain Development

Frontiers in Pediatrics

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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

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Visual Impairment in FOXG1-mutated Individuals and Mice

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FOXG1 Orchestrates Neocortical Organization and Cortico-Cortical Connections

English

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

Molecular Cytogenetics

Molecular Medicine

Molecular Biology

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

Internal Medicine

Molecular Biology

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

Neural Development

Developmental Neuroscience

English

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

Journal of Neuroscience

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

Clinical Genetics

English