Last Updated: 09/26/2026
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Found 12 publications
Research Recommendations From the National Institutes of Health Workshop on Predicting, Preventing, and Treating Preeclampsia.
Journal: Hypertension (Dallas, Tex. : 1979)
Published: January 29, 2019
Whole exome sequencing identifies hemizygous deletions in the UGT2B28 and USP17L2 genes in a three‑generation family with endometriosis.
Journal: Molecular medicine reports
Published: November 05, 2018
Co-existence of endometriosis with 13 non-gynecological co-morbidities: Mutation analysis by whole exome sequencing.
Journal: Molecular medicine reports
Published: July 23, 2018
Initial Experience and Usage Patterns With the Owlet Smart Sock Monitor in 47,495 Newborns.
Journal: Global pediatric health
Published: October 19, 2017
Analytical and Clinical Validity Study of FirstStepDx PLUS: A Chromosomal Microarray Optimized for Patients with Neurodevelopmental Conditions.
Journal: PLoS currents
Published: March 31, 2017
KBG syndrome involving a single-nucleotide duplication in ANKRD11.
Journal: Cold Spring Harbor molecular case studies
Published: December 01, 2016
SCN8A mutation in a child presenting with seizures and developmental delays.
Journal: Cold Spring Harbor molecular case studies
Published: December 01, 2016
Genes Linked to Endometriosis by GWAS Are Integral to Cytoskeleton Regulation and Suggests That Mesothelial Barrier Homeostasis Is a Factor in the Pathogenesis of Endometriosis.
Journal: Reproductive sciences (Thousand Oaks, Calif.)
Published: July 30, 2016
Genome-wide association study link novel loci to endometriosis.
Journal: PloS one
Published: October 07, 2012
Showing 1-12 of 12
Last Updated: 09/26/2026