A Shared Founder Mutation Underlies Restrictive Dermopathy in Old Colony (Dutch-German) Mennonite and Hutterite Patients in North America

Lignende værker

• Amish, Mennonite, and Hutterite Genetic Disorder Database
  af: Payne, Michael, et al.
  Udgivet: (2011)
• A Dutch Fanconi Anemia FANCC Founder Mutation in Canadian Manitoba Mennonites
  af: de Vries, Yne, et al.
  Udgivet: (2012)
• FANCC Dutch founder mutation in a Mennonite family from Tamaulipas, México
  af: García‐de Teresa, Benilde, et al.
  Udgivet: (2019)
• Development of a diagnostic DNA chip to screen for 30 autosomal recessive disorders in the Hutterite population
  af: Triggs‐Raine, Barbara, et al.
  Udgivet: (2016)
• Matching two independent cohorts validates DPH1 as a gene responsible for autosomal recessive intellectual disability with short stature, craniofacial and ectodermal anomalies
  af: Loucks, Catrina M., et al.
  Udgivet: (2015)