Publications by authors named "Hazel Perry"

9Publications

Case Report of Floating-Harbor Syndrome With Bilateral Cleft Lip.

Cleft Palate Craniofac J 2020 01 27;57(1):132-136. Epub 2019 Jun 27.

Program in Craniofacial Biology and Division of Craniofacial Anomalies, Department of Orofacial Sciences, University of California, San Francisco, CA, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1177/1055665619858257DOI Listing
January 2020

DLX4 is associated with orofacial clefting and abnormal jaw development.

Hum Mol Genet 2015 Aug 7;24(15):4340-52. Epub 2015 May 7.

Department of Pediatrics, University of California, San Francisco, San Francisco, CA 94143, USA, Institute for Human Genetics, University of California, San Francisco, San Francisco, CA, USA,

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/hmg/ddv167DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4492397PMC
August 2015

Clefting in trisomy 9p patients: genotype-phenotype correlation using microarray comparative genomic hybridization.

J Craniofac Surg 2010 Sep;21(5):1376-9

Division of Medical Genetics, Department of Pediatrics, University of California, San Francisco, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/SCS.0b013e3181ef2bbfDOI Listing
September 2010

A novel EFNB1 mutation (c.712delG) in a family with craniofrontonasal syndrome and diaphragmatic hernia.

Am J Med Genet A 2010 Oct;152A(10):2574-7

Department of Pediatrics, University of California, San Francisco, California 94143-0706, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.33596DOI Listing
October 2010

Novel FGFR2 deletion in a patient with Beare-Stevenson-like syndrome.

Am J Med Genet A 2009 Aug;149A(8):1814-7

Department of Pediatrics, University of California, San Francisco, 94143-0748, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.32947DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2785435PMC
August 2009

Autism spectrum disorders and attention-deficit/hyperactivity disorder in boys with the fragile X premutation.

J Dev Behav Pediatr 2006 Apr;27(2 Suppl):S137-44

Medical Investigation of Neurodevelopmental Disorders (M.I.N.D.) Institute, University of California, Davis, CA, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/00004703-200604002-00012DOI Listing
April 2006