Publications by authors named "Jay W Ellison"

24Publications

Refinement of the 8q22.1 microdeletion critical region associated with Nablus mask-like facial syndrome.

Am J Med Genet A 2014 Jan 20;164A(1):259-63. Epub 2013 Nov 20.

Signature Genomic Laboratories, PerkinElmer, Inc., Spokane, Washington.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.36163DOI Listing
January 2014

Genetic basis of intellectual disability.

Annu Rev Med 2013 27;64:441-50. Epub 2012 Sep 27.

Signature Genomic Laboratories, PerkinElmer, Inc., Spokane, Washington 99207, USA.

View Article

Download full-text PDF

Source
http://www.annualreviews.org/doi/10.1146/annurev-med-042711-
Publisher Site
http://dx.doi.org/10.1146/annurev-med-042711-140053DOI Listing
July 2013

A novel NDP mutation in an infant with unilateral persistent fetal vasculature and retinal vasculopathy.

Ophthalmic Genet 2009 Jun;30(2):99-102

Mayo Clinic College of Medicine, Mayo Clinic and Mayo Foundation, Rochester, Minnesota 55905, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1080/13816810802705755DOI Listing
June 2009

Evidence of genetic locus heterogeneity for familial bicuspid aortic valve.

J Surg Res 2007 Sep;142(1):28-31

Department of Medical Genetics, Mayo Clinic College of Medicine, Rochester, Minnesota 55905, USA.

View Article

Download full-text PDF

Source
http://linkinghub.elsevier.com/retrieve/pii/S002248040600593
Publisher Site
http://dx.doi.org/10.1016/j.jss.2006.04.040DOI Listing
September 2007

Microarray comparative genomic hybridization and FISH studies of an unbalanced cryptic telomeric 2p deletion/16q duplication in a patient with mental retardation and behavioral problems.

Am J Med Genet A 2007 Apr;143A(7):746-51

Cytogenetics Laboratory, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN 55905, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.31645DOI Listing
April 2007

Subglottic stenosis in short-statured children: a case for further investigation of airway symptoms in patients with skeletal dysplasias.

Int J Pediatr Otorhinolaryngol 2006 Jan 5;70(1):147-53. Epub 2005 Oct 5.

Division of Pediatric Otolaryngology, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ijporl.2005.05.031DOI Listing
January 2006

Trisomy 20 mosaicism caused by a maternal meiosis II error is associated with normal intellect but multiple congenital anomalies.

Am J Med Genet A 2005 Apr;134A(2):202-6

Department of Medical Genetics, Mayo Clinic College of Medicine, Rochester, Minnesota, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.30586DOI Listing
April 2005

Molecular characterization of a ring X chromosome in a male with short stature.

Hum Genet 2002 Apr 2;110(4):322-6. Epub 2002 Mar 2.

Department of Medical Genetics, Mayo Clinic, 200 First St. SW, Rochester, MN 55905, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00439-002-0685-7DOI Listing
April 2002