Progress in familial hypertrophic cardiomyopathy: molecular genetic analyses in the original family studied by Teare.

Samankaltaisia teoksia

• A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2.
  Tekijä: Thierfelder, L, et al.
  Julkaistu: (1993)
• Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations.
  Tekijä: Watkins, H, et al.
  Julkaistu: (1992)
• Independent origin of identical beta cardiac myosin heavy-chain mutations in hypertrophic cardiomyopathy.
  Tekijä: Watkins, H, et al.
  Julkaistu: (1993)
• Familial hypertrophic cardiomyopathy is a genetically heterogeneous disease.
  Tekijä: Solomon, S D, et al.
  Julkaistu: (1990)
• Syncope in hypertrophic cardiomyopathy.
  Tekijä: McKenna, W, et al.
  Julkaistu: (1982)