Hazel Perry
Genetic Counselor III
Craniofacial Anomalies
Chancellor/EVC/FAS

Websites

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• Clinical Profile at UCSF Benioff Children's Hospital (ucsfbenioffchildrens.org)

Publications (7)

Top publication keywords:
Homeodomain ProteinsZebrafish ProteinsComparative Genomic HybridizationCraniofacial AbnormalitiesHeart Septal Defects, VentricularHernia, DiaphragmaticGene DeletionGrowth DisordersJaw AbnormalitiesCleft PalateEphrin-B1Chromosomes, Human, Pair 9Abnormalities, MultipleCleft LipReceptor, Fibroblast Growth Factor, Type 2

• Publisher Correction: Application of full-genome analysis to diagnose rare monogenic disorders.
  NPJ genomic medicine 2021 Shieh JT, Penon-Portmann M, Wong KHY, Levy-Sakin M, Verghese M, Slavotinek A, Gallagher RC, Mendelsohn BA, Tenney J, Beleford D, Perry H, Chow SK, Sharo AG, Brenner SE, Qi Z, Yu J, Klein OD, Martin D,…
• Application of full-genome analysis to diagnose rare monogenic disorders.
  NPJ genomic medicine 2021 Shieh JT, Penon-Portmann M, Wong KHY, Levy-Sakin M, Verghese M, Slavotinek A, Gallagher RC, Mendelsohn BA, Tenney J, Beleford D, Perry H, Chow SK, Sharo AG, Brenner SE, Qi Z, Yu J, Klein OD, Martin D,…
• Case Report of Floating-Harbor Syndrome With Bilateral Cleft Lip.
  The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2019 Ko J, Pomerantz JH, Perry H, Shieh JT, Slavotinek AM, Oberoi S, Klein OD
• DLX4 is associated with orofacial clefting and abnormal jaw development.
  Human molecular genetics 2015 Wu D, Mandal S, Choi A, Anderson A, Prochazkova M, Perry H, Gil-Da-Silva-Lopes VL, Lao R, Wan E, Tang PL, Kwok PY, Klein O, Zhuan B, Slavotinek AM
• A novel EFNB1 mutation (c.712delG) in a family with craniofrontonasal syndrome and diaphragmatic hernia.
  American journal of medical genetics. Part A 2010 Hogue J, Shankar S, Perry H, Patel R, Vargervik K, Slavotinek A
• Clefting in trisomy 9p patients: genotype-phenotype correlation using microarray comparative genomic hybridization.
  The Journal of craniofacial surgery 2010 Jelin A, Perry H, Hogue J, Oberoi S, Cotter PD, Klein OD
• Novel FGFR2 deletion in a patient with Beare-Stevenson-like syndrome.
  American journal of medical genetics. Part A 2009 Slavotinek A, Crawford H, Golabi M, Tao C, Perry H, Oberoi S, Vargervik K, Friez M