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Erin L Youngs

TitleClinical Assistant Professor
InstitutionUniversity of Oklahoma Health Sciences Center
DepartmentDept of Pediatrics
Address1200 Children's Ave
Oklahoma City OK 73104-4600
Phone405/271-8685
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    1. Butler MG, Youngs EL, Roberts JL, Hellings JA. Assessment and treatment in autism spectrum disorders: a focus on genetics and psychiatry. Autism Res Treat. 2012; 2012:242537. PMID: 22934170; PMCID: PMC3420490.
    2. Youngs EL, Henkhaus RS, Hellings JA, Butler MG. 12-year-old boy with a 4q35.2 microdeletion and involvement of MTNR1A, FAT1, and F11 genes. Clin Dysmorphol. 2012 Apr; 21(2):93-6. PMID: 22127048.
      View in: PubMed
    3. Youngs EL, Dasouki M, Butler MG. 14q32 deletion syndrome: a clinical report. Clin Dysmorphol. 2012 Jan; 21(1):42-4. PMID: 22143351.
      View in: PubMed
    4. Youngs EL, Henkhaus R, Hellings JA, Butler MG. IL1RAPL1 gene deletion as a cause of X-linked intellectual disability and dysmorphic features. Eur J Med Genet. 2012 Jan; 55(1):32-6. PMID: 21933724.
      View in: PubMed
    5. Youngs EL, Hellings JA, Butler MG. A clinical report and further delineation of the 14q32 deletion syndrome. Clin Dysmorphol. 2011 Jul; 20(3):143-7. PMID: 21358539.
      View in: PubMed
    6. Youngs EL, Hellings JA, Butler MG. ANKRD11 gene deletion in a 17-year-old male. Clin Dysmorphol. 2011 Jul; 20(3):170-1. PMID: 21527850.
      View in: PubMed
    7. Dasouki MJ, Youngs EL, Hovanes K. Structural Chromosome Abnormalities Associated with Obesity: Report of Four New subjects and Review of Literature. Curr Genomics. 2011 May; 12(3):190-203. PMID: 22043167; PMCID: PMC3137004.
    8. Burnside RD, Pasion R, Mikhail FM, Carroll AJ, Robin NH, Youngs EL, Gadi IK, Keitges E, Jaswaney VL, Papenhausen PR, Potluri VR, Risheg H, Rush B, Smith JL, Schwartz S, Tepperberg JH, Butler MG. Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay. Hum Genet. 2011 Oct; 130(4):517-28. PMID: 21359847.
      View in: PubMed
    9. Youngs EL, McCord T, Hellings JA, Spinner NB, Schneider A, Butler MG. An 18-year follow-up report on an infant with a duplication of 9q34. Am J Med Genet A. 2010 Jan; 152A(1):230-3. PMID: 20034079.
      View in: PubMed
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