阿摩線上測驗
64.凝血第八因子缺乏（A型血友病）的遺傳方式是：
(A)自體顯性遺傳異常
(B)自體隱性遺傳異常
(C)自體共顯性遺傳異常（autosomal codominant）
(D)X-聯結異常（X-linked disorder）
答案：登入後查看
統計： A(175), B(319), C(59), D(575), E(0) #1111472
統計： A(175), B(319), C(59), D(575), E(0) #1111472
詳解 (共 2 筆)
Chris
#2913078
von Willebrand disease types I and II are inherited in an autosomal dominant pattern.
There are two main types of haemophilia: haemophilia A, which occurs due to not enough clotting factor VIII, and haemophilia B, which occurs due to not enough clotting factor IX. They are typically inherited from one's parents through an X chromosome with a nonfunctional gene.
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