Rech, Megan E.
Megan E Rech researcher (ORCID 0000-0002-3037-2521)
VIAF ID: 4276160122846640630008 ( Personal )
Permalink: http://viaf.org/viaf/4276160122846640630008
Preferred Forms
4xx's: Alternate Name Forms (1)
Works
| Title | Sources |
|---|---|
| Magel2 Modulates Bone Remodeling and Mass in Prader-Willi Syndrome by Affecting Oleoyl Serine Levels and Activity |
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| Nr2f1 heterozygous knockout mice recapitulate neurological phenotypes of Bosch-Boonstra-Schaaf optic atrophy syndrome and show impaired hippocampal synaptic plasticity |
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| Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomalies |
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| Schaaf-Yang syndrome overview: Report of 78 individuals |
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