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Paper Details

Skewed X-chromosome inactivation in unsolved neurodevelopmental disease cases can guide re-evaluation For X-linked genes.
Eur J Hum Genet
4
2023
ATRX, FRAXA, HhaI, KDM5C, NDD, OTUD5, PDZD4, PHF6, TAF1, X chromosome, X-chromosome, X-linked disorders, X-linked genes, X-linked variants, ZMYM3, genetic variants, inactive X chromosome allele, long-DNA, neurodevelopmental disease, neurodevelopmental disorder, patients
Author NameAffiliation
Silvia De RubeisSeaver Autism Center for Research and Treatment, Icahn School of Medicine at Mount Sinai
Silvia De RubeisThe Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai
Silvia De RubeisIcahn School of Medicine at Mount Sinai
Joseph D BuxbaumSeaver Autism Center for Research and Treatment, Icahn School of Medicine at Mount Sinai
Joseph D BuxbaumIcahn School of Medicine at Mount Sinai
Joseph D BuxbaumIcahn School of Medicine at Mount Sinai
Joseph D BuxbaumFriedman Brain Institute, Icahn School of Medicine at Mount Sinai
Joseph D BuxbaumThe Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai
Joseph D BuxbaumIcahn School of Medicine at Mount Sinai
Joseph D BuxbaumSeaver Autism Center for Research and Treatment, Icahn School of Medicine at Mount Sinai
Joseph D BuxbaumIcahn School of Medicine at Mount Sinai
Joseph D BuxbaumThe Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai
Joseph D BuxbaumFriedman Brain Institute, Icahn School of Medicine at Mount Sinai
Joseph D BuxbaumIcahn School of Medicine at Mount Sinai
Joseph D BuxbaumIcahn School of Medicine at Mount Sinai
Marco TartagliaIRCCS
Massimo DelledonneUniversity of Verona
Giovanni Battista FerreroUniversity of Turin
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