Cara M Skraban (Cara Skraban)

Years Active: 2020-2021
Publications (10 Years): 4

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

Publications

Alanna Strong, Cara M Skraban, Kevin Meyers, Sandra Amaral, Susan Furth, Stacey Drant, Wendy Hsiao, Lauren Galea, Jessica Gold, Nina B Gold, Jacqueline Leonard, Sonya Lopez, Elaine H Zackai, Reed E Pyeritz
Expanding the phenotypic spectrum of Mendelian connective tissue disorders to include prominent kidney phenotypes. American journal of medical genetics. Part A 185 (12) (2021)
Katheryn Grand, Cara M Skraban, Jennifer L Cohen, Leah Dowsett, Sarah Mazzola, Jennifer Tarpinian, Emma Bedoukian, Addie Nesbitt, Beth Denenberg, Lauren Lulis, Avni Santani, Elaine H Zackai, Matthew A Deardorff
Nonlethal presentations of CYP26B1-related skeletal anomalies and multiple synostoses syndrome. American journal of medical genetics. Part A 185 (9) (2021)
Alanna Strong, Dong Li, Frank Mentch, Emma C Bedoukian, Erum A Hartung, Kevin Meyers, Cara M Skraban, Jessica Wen, Livija Medne, Joseph Glessner, Deborah Watson, Ian Krantz, Hakon H Hakonarson
Ciliopathies: Coloring outside of the lines. American journal of medical genetics. Part A 185 (3) (2020)
Alyssa L Ritter, Petra Werner, Brande Latney, Bryon L Krock, Avni Santani, Emma C Bedoukian, Cara M Skraban, Matthew A Deardorff, Elizabeth Goldmuntz
NKX2-6 related congenital heart disease: Biallelic homeodomain-disrupting variants and truncus arteriosus. American journal of medical genetics. Part A 182 (6) (2020)

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