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Publications by Britt Marie Anderlid

Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy

American Journal of Human Genetics
Genetics
2019English

Characterization of Deletions at 9p Affecting the Candidate Regions for Sex Reversal and Deletion 9p Syndrome by MLPA

European Journal of Human Genetics
Genetics
2009English

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