Publications by authors named "Erin L Youngs"

9Publications

Assessment and treatment in autism spectrum disorders: a focus on genetics and psychiatry.

Authors:
Merlin G Butler Erin L Youngs Jennifer L Roberts Jessica A Hellings

Autism Res Treat 2012 31;2012:242537. Epub 2012 May 31.

Department of Psychiatry and Behavioral Sciences, Kansas University Medical Center, 3901 Rainbow Blvd., MS4015, Kansas City, KS 66160, USA.

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August 2012

14q32 deletion syndrome: a clinical report.

Authors:
Erin L Youngs Majed Dasouki Merlin G Butler

Clin Dysmorphol 2012 Jan;21(1):42-4

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January 2012

12-year-old boy with a 4q35.2 microdeletion and involvement of MTNR1A, FAT1, and F11 genes.

Authors:
Erin L Youngs Rebecca S Henkhaus Jessica A Hellings Merlin G Butler

Clin Dysmorphol 2012 Apr;21(2):93-6

Department of Psychiatry and Behavioral Sciences, Kansas University Medical, Center, Kansas City, Kansas, USA.

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April 2012

Structural Chromosome Abnormalities Associated with Obesity: Report of Four New subjects and Review of Literature.

Authors:
Majed J Dasouki Erin L Youngs Karine Hovanes

Curr Genomics 2011 May;12(3):190-203

Departments of Pediatrics and Internal Medicine, Kansas University Medical Center, Kansas City, Kansas, USA.

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May 2011

IL1RAPL1 gene deletion as a cause of X-linked intellectual disability and dysmorphic features.

Authors:
Erin L Youngs Rebecca Henkhaus Jessica A Hellings Merlin G Butler

Eur J Med Genet 2012 Jan 10;55(1):32-6. Epub 2011 Sep 10.

Department of Psychiatry and Behavioral Sciences, University of Kansas Medical Center, Kansas City, KS, United States.

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January 2012

ANKRD11 gene deletion in a 17-year-old male.

Authors:
Erin L Youngs Jessica A Hellings Merlin G Butler

Clin Dysmorphol 2011 Jul;20(3):170-1

Department of Psychiatry and Behavioral Sciences, Kansas University Medical Center, 3901 Rainbow Blvd., Kansas City, KS 66160, USA.

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July 2011

Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay.

Authors:
Rachel D Burnside Romela Pasion Fady M Mikhail Andrew J Carroll Nathaniel H Robin Erin L Youngs Inder K Gadi Elizabeth Keitges Vikram L Jaswaney Peter R Papenhausen Venkateswara R Potluri Hiba Risheg Brooke Rush Janice L Smith Stuart Schwartz James H Tepperberg Merlin G Butler

Hum Genet 2011 Oct 27;130(4):517-28. Epub 2011 Feb 27.

Laboratory Corporation of America, 1904 Alexander Dr., Research Triangle Park, NC 27709, USA.

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October 2011

A clinical report and further delineation of the 14q32 deletion syndrome.

Authors:
Erin L Youngs Jessica A Hellings Merlin G Butler

Clin Dysmorphol 2011 Jul;20(3):143-7

Department of Psychiatry and Behavioral Sciences, Kansas University Medical Center, 3901 Rainbow Blvd, Kansas City, KS 66160, USA.

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July 2011

An 18-year follow-up report on an infant with a duplication of 9q34.

Authors:
Erin L Youngs Timothy McCord Jessica A Hellings Nancy B Spinner Adele Schneider Merlin G Butler

Am J Med Genet A 2010 Jan;152A(1):230-3

Departments of Psychiatry & Behavioral Sciences and Pediatrics, University of Kansas Medical Center, Kansas City, Kansas, USA.

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January 2010