Robert F. Stratton
Medical Genetics | Pediatrics
3533 S Alameda St
Corpus Christi, TX 78411
Corpus Christi, TX 78411
Last Updated: 09/26/2026
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Found 6 publications
Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders.
Journal: Genome medicine
Published: September 04, 2020
Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome.
Journal: Nature genetics
Published: August 27, 2020
Phenotypic spectrum and transcriptomic profile associated with germline variants in TRAF7.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: November 13, 2019
Case of 7p22.1 Microduplication Detected by Whole Genome Microarray (REVEAL) in Workup of Child Diagnosed with Autism.
Journal: Case reports in genetics
Published: October 02, 2014
Establishing a reference group for distal 18q-: clinical description and molecular basis.
Journal: Human genetics
Published: June 13, 2013
Metastatic medulloblastoma in an adolescent with Simpson-Golabi-Behmel syndrome.
Journal: American journal of medical genetics. Part A
Published: October 11, 2011
Showing 1-6 of 6
Last Updated: 09/26/2026