Roy E Weiss (R E Weiss)

Publication Activity (10 Years)

Years Active: 2018-2021
Publications (10 Years): 2

Top Topics

Intellectual Disability

Genome Wide Analysis

Top Venues

BMC medical genetics

Thyroid : official journal of the American Thyroid Association

This page only lists publications with an associated author ORCID identifier.

Publications

Aryel Furman, Zeina Hannoush, Francisco Barrera Echegoyen, Alexandra M Dumitrescu, Samuel Refetoff, Roy E Weiss
Novel DIO1 Gene Mutation Acting as Phenotype Modifier for Novel Compound Heterozygous TPO Gene Mutations Causing Congenital Hypothyroidism. Thyroid : official journal of the American Thyroid Association 31 (10) (2021)
Y Watanabe, E Sharwood, B Goodwin, M K Creech, H Y Hassan, M G Netea, M Jaeger, A Dumitrescu, S Refetoff, T Huynh, Roy E Weiss
A novel mutation in the TG gene (G2322S) causing congenital hypothyroidism in a Sudanese family: a case report. BMC medical genetics 19 (1) (2018)