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Heather M Byers

Years Active: 2017-2020
Publications (10 Years): 5

Stanford University School of Medicine

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Stanford University School of Medicine Jul 17o 2017

United States

Assistant Professor :: Division of Medical Genetics

Publications

Debra S Regier, Wendy E Smith, Heather M Byers
Medical genetics education in the midst of the COVID-19 pandemic: Shared resources. American journal of medical genetics. Part A 182 (6) (2020)
Heather M Byers, Whitney Neufeld-Kaiser, Edith Y Chang, Karen Tsuchiya, Erin S Oehler, Margaret P Adam
Discordant sex between fetal screening and postnatal phenotype requires evaluation. Journal of perinatology : official journal of the California Perinatal Association 39 (1) (2018)
Heather M Byers, Dana M Jensen, Ian A Glass, James T Bennett
Minimal mosaicism, maximal phenotype: Discordance between clinical and molecular findings in two patients with tuberous sclerosis. American journal of medical genetics. Part C, Seminars in medical genetics 178 (3) (2018)
Heather M Byers, Maida Chen, Andrew S Gelfand, Bruce Ong, Marisa Jendras, Ian A Glass
Expanding the phenotype of congenital central hypoventilation syndrome impacts management decisions. American journal of medical genetics. Part A 176 (6) (2018)
Heather M Byers, Lauren H Mohnach, Patricia Y Fechner, Ming Chen, Inas H Thomas, Linda A Ramsdell, Margarett Shnorhavorian, Elizabeth A McCauley, Anne-Marie E Amies Oelschlager, John M Park, David E Sandberg, Margaret P Adam, Catherine E Keegan
Unexpected ethical dilemmas in sex assignment in 46,XY DSD due to 5-alpha reductase type 2 deficiency. American journal of medical genetics. Part C, Seminars in medical genetics 175 (2) (2017)

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