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Topic
- Cardiac System
- Clinical Case Report
- Diagnostic Development
- Disease Discovery
- Endocrine System
- Endophenotype
- Genomic Testing
- Hearing
- Hepatic System
- Immune System
- Laboratory
- Metabolic
- Mitochondrial
- Natural History
- Neurologic System
- Ocular System
- Opinion
- Pathophysiology
- Population Genetics
- Psychiatry
- Public Health
- Pulmonology
- Renal System
- Review
- Skeletal System
- Therapy
- Year
Papers Published in 2016
Authors: Manoli I, Myles JG, Sloan JL, Carrillo-Carrasco N, Morava E, Strauss KA, Morton H, Venditti CP
Authors: Motzek A, Knezevic J, Switzeny OJ, Cooper A, Baric I, Beluzic R, Strauss KA, Puffenberger EG, Mudd SH, Vugrek O, Zechner U
Authors: Feier F, Schwartz IV, Benkert AR, Neto JS, Miura I, Chapchap P, da Fonseca EA, Vieira S, Zanotelli ML, Vairo FP, Camelo JS Jr, Margutti AV, Mazariegos GV, Puffenberger EG, Strauss KA
Authors: Kochunov P, Fu M, Nugent K, Wright SN, Du X, Muellerklein F, Morrissey M, Eskandar G, Shukla DK, Jahanshad N, Thompson PM, Patel B, Postolache TT, Strauss KA, Shuldiner AR, Mitchell BD, Hong LE
Support our mission of providing compassionate, affordable, and efficient care to families facing rare genetic disorders!
Our clinic serves as a trusted medical practice for children and adults facing rare genetic disorders. Our dedicated team works every day to prevent and treat genetic illnesses. Our facility is in the heart of the Amish and Mennonite communities in Lancaster County. Inside is filled with cutting-edge gene sequencing tools that allow us to deliver highly personalized care—a precise treatment option for the right patient at the right time.