Isolated growth hormone deficiency: Two families with autosomal dominant inheritance

Παρόμοια τεκμήρια

• Selective gamma-A-globulin deficiency, with dominant autosomal inheritance in a Swiss family.
  ανά: Stocker, F., κ.ά.
  Έκδοση: (1968)
• Familial sinus node dysfunction with autosomal dominant inheritance.
  ανά: Lehmann, H, κ.ά.
  Έκδοση: (1978)
• Familial hypothyroidism with autosomal dominant inheritance.
  ανά: Mimouni, M, κ.ά.
  Έκδοση: (1996)
• Familial pulmonary hypertension. Evidence of autosomal dominant inheritance.
  ανά: Thompson, P, κ.ά.
  Έκδοση: (1970)
• Familial aggregation of streptomycin ototoxicity: autosomal dominant inheritance?
  ανά: Viljoen, D L, κ.ά.
  Έκδοση: (1983)