A further patient with Pai syndrome with autosomal dominant inheritance?

Những quyển sách tương tự

• Evidence of autosomal dominant mutations in childhood-onset proximal spinal muscular atrophy.
  Bằng: Rudnik-Schöneborn, S., et al.
  Được phát hành: (1994)
• Childhood onset autosomal dominant polycystic kidney disease in sibs: clinical picture and recurrence risk. German Working Group on Paediatric Nephrology (Arbeitsgemeinschaft für Pädiatrische Nephrologie.
  Bằng: Zerres, K, et al.
  Được phát hành: (1993)
• Autosomal dominant inheritance of Weaver syndrome.
  Bằng: Fryer, A, et al.
  Được phát hành: (1997)
• Apparent autosomal recessive inheritance in families with proximal spinal muscular atrophy affecting individuals in two generations.
  Bằng: Rudnik-Schöneborn, S., et al.
  Được phát hành: (1996)
• Autosomal dominant inheritance of Gerhardt's syndrome in three generations of a family.
  Bằng: Morelli, G, et al.
  Được phát hành: (1980)