Clinical utility gene card for: Prader-Willi Syndrome

समान संसाधन

• Clinical utility gene card for: Angelman Syndrome
  द्वारा: Buiting, Karin, और अन्य
  प्रकाशित: (2015)
• Epimutations in Prader-Willi and Angelman Syndromes: A Molecular Study of 136 Patients with an Imprinting Defect
  द्वारा: Buiting, Karin, और अन्य
  प्रकाशित: (2003)
• Prader–Willi syndrome
  द्वारा: Cassidy, Suzanne B, और अन्य
  प्रकाशित: (2009)
• Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype.
  द्वारा: Gillessen-Kaesbach, G, और अन्य
  प्रकाशित: (1994)
• A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader–Willi syndrome
  द्वारा: Kanber, Deniz, और अन्य
  प्रकाशित: (2009)