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生物必修2知识(Biology requires 2 knowledge)
生物必修2知识(Biology requires 2 knowledge)
1. The concept: a genetic disease controlled by a peer allele.
2. Reason: human genetic diseases are human diseases caused by the change of genetic material
3, characteristics: inherited by the family, high incidence (about 20%--25%) in our country
4, type:
Dominant genetic disease associated with X: vitamin D rickets
Often manifested: multiple fingers, fingers, or cartilage hypoplasia
Recessive inherited disease associated with X: color blindness, hemophilia
Congenital, deaf, albinism, sickle cell anemia, phenylketonuria, phenylketonuria
(two) polygenic inheritance disease
1. Concept: human genetic disease controlled by multiple alleles.
2 common types: cleft palate, anencephaly, hypertension, juvenile diabetes etc..
(three) hereditary diseases of chromosome abnormalities (referred to as chromosomal diseases)
1. Concept: genetic disorders caused by chromosomal abnormalities. (including abnormal numbers and structural abnormalities)
2, type:
Autosomal genetic disease: structural abnormalities of Cushings syndrome
Abnormal number: trisomy 21 (congenital mental retardation)
Sex chromosome genetic disorders: gonadal dysgenesis syndrome (type XO, absence of a X chromosome)
1, the law of segregation in biological cells, there are pairs of genetic factor the same trait, dont mix; during the formation of gametes, pairs of genetic factor separation, genetic factors separated respectively into different gametes, with gametes offspring.
2, free combination law: separation and combination of genetic factors controlling different characters that do not interfere with each other; during the formation of gametes, genetic factor in determining the same character pairs are separated from each other, free combination of genetic factors determine different traits.
The essence of the 3 and two basic laws of heredity is that heredity is not the trait itself, but the genetic factor controlling the trait.
4 reasons, Mendels success: selection of expe
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