Publications by authors named "Janice Zunich"

7 Publications

  • Page 1 of 1

Clinical features of trisomy 12 mosaicism-Report and review.

Am J Med Genet A 2017 Jun 27;173(6):1681-1686. Epub 2017 Mar 27.

Department of Pathology, University of Utah, Salt Lake City, Utah.

View Article and Find Full Text PDF
June 2017

Mutations in the glycosylphosphatidylinositol gene PIGL cause CHIME syndrome.

Am J Hum Genet 2012 Apr 22;90(4):685-8. Epub 2012 Mar 22.

Genetic Disease Program, Sanford Children's Health Research Center, Sanford-Burnham Medical Research Institute, La Jolla, CA 92037, USA.

View Article and Find Full Text PDF
April 2012

A novel dominant negative mutation of OTX2 associated with combined pituitary hormone deficiency.

J Clin Endocrinol Metab 2008 Nov 26;93(11):4351-9. Epub 2008 Aug 26.

Division of Pediatric Endocrinology, The Johns Hopkins University School of Medicine, 600 North Wolfe Street, CMSC 406, Baltimore, Maryland 21287, USA.

View Article and Find Full Text PDF
November 2008

A child with deletion (14)(q24.3q32.13) and auditory neuropathy.

Am J Med Genet A 2008 Jan;146A(1):117-23

Department of Medical Genetics, University of Alberta, Edmonton, AB, Canada.

View Article and Find Full Text PDF
January 2008

Familial interstitial duplication of 11q; partial trisomy (11)(q13.5q21).

Am J Med Genet A 2004 May;126A(4):423-6

Indiana University School of Medicine, Northwest Center for Medical Education, Gary, Indiana 46408, USA.

View Article and Find Full Text PDF
May 2004