14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype - Concepedia

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14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype

DOI Full Paper Access

76

Citations

32

References

2012

Year

Carolyn Ellaway, Gladys Ho, Elisa Bettella, Alisa Knapman, Felicity Collins, Anna Hackett, F. Ellis McKenzie, Artur Darmanian, Gregory B. Peters, Kerry Fagan,

European Journal of Human Genetics

Developmental AnomalyDevelopmental BiologyGenetic DisorderGeneticsPathologyMolecular GeneticsMedicineVariant InterpretationClinical Genetics

References

	Year	Citations

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