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Hazel Perry

Genetic counselor

Hazel Perry is a genetic counselor at the Prenatal Diagnosis Center and at the Craniofacial Anomalies Clinic. She has a special interest in craniofacial-related genetic syndromes.

Perry received her bachelor's degree in psychology, with an emphasis in biology, from the University of California, Davis, and her master's degree in genetic counseling from Northwestern University. She is certified by the American Board of Genetic Counseling.

Clinics

Prenatal Diagnostic Center
350 Parnassus Ave., Suite 810
San Francisco, CA 94117
Phone: (415) 476-4080
Fax: (415) 353-4077

Hours: Monday to Friday
8 a.m. – 5 p.m.

Selected Research and Publications

  1. Hogue J, Shankar S, Perry H, Patel R, Vargervik K, Slavotinek A. 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.
  2. Jelin A, Perry H, Hogue J, Oberoi S, Cotter PD, Klein OD. Clefting in trisomy 9p patients: genotype-phenotype correlation using microarray comparative genomic hybridization. J Craniofac Surg. 2010 Sep; 21(5):1376-9.
  3. Slavotinek A, Crawford H, Golabi M, Tao C, Perry H, Oberoi S, Vargervik K, Friez M. Novel FGFR2 deletion in a patient with Beare-Stevenson-like syndrome. Am J Med Genet A. 2009 Aug; 149A(8):1814-7.

Publications are derived from MEDLINE/PubMed and provided by UCSF Profiles, a service of the Clinical & Translational Science Institute (CTSI) at UCSF. Researchers can make corrections and additions to their publications by logging on to UCSF Profiles.

This health care professional is not a member of UCSF Medical Group. Please check with your health insurance plan regarding coverage for services.