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Phenotypic variability inHey2 −/−mice and absence ofHEY2mutations in patients with congenital heart defects or Alagille syndrome

✍ Scribed by Andreas Fischer; Barbara Klamt; Nina Schumacher; Christiane Glaeser; Ingo Hansmann; Hartmut Fenge; Manfred Gessler

No coin nor oath required. For personal study only.

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