The Moroccan human mutation database

Ítems similars

• A recurrent mutation in Moroccan patients with Dyggve-Melchior-Clausen syndrome: Report of a new case and review
  per: Elalaoui, Siham Chafai, et al.
  Publicat: (2011)
• Novel nonsense mutation of BRCA2 gene in a Moroccan man with familial breast cancer
  per: Guaoua, Soukaina, et al.
  Publicat: (2014)
• The Bedouin mutation c.155-166del of the TBCE gene in a patient with Sanjad-Sakati syndrome of Moroccan origin
  per: Ratbi, Ilham, et al.
  Publicat: (2015)
• Moroccan consanguineous family with Becker myotonia and review
  per: Ratbi, Ilham, et al.
  Publicat: (2011)
• A Novel Mutation in the Endothelin B Receptor Gene in a Moroccan Family with Shah-Waardenburg Syndrome
  per: Doubaj, Yassamine, et al.
  Publicat: (2015)