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Nathan D Kopp
(Nathan Kopp)
ORCID
Publication Activity (10 Years)
Years Active: 2018-2020
Publications (10 Years): 2
Top Topics
Intellectual Disability
Copy Number
Case Control
Autism Spectrum Disorder
Top Venues
Molecular genetics & genomic medicine
American journal of medical genetics. Part A
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This page only lists publications with an associated author ORCID identifier.
Publications
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Nathan D Kopp
,
Ina Amarillo
,
Julian A Martinez
,
Fabiola Quintero-Rivera
Pathogenic paternally inherited NLGN4X deletion in a female with autism spectrum disorder: Clinical, cytogenetic, and molecular characterization.
American journal of medical genetics. Part A
185 (3) (2020)
Nathan D Kopp
,
Phoebe C R Parrish
,
Michael Lugo
,
Joseph D Dougherty
,
Beth A Kozel
Exome sequencing of 85 Williams-Beuren syndrome cases rules out coding variation as a major contributor to remaining variance in social behavior.
Molecular genetics & genomic medicine
6 (5) (2018)