Quizizz 112-1 Pathology-CH06         Heredity-89

Quizizz 112-1 Pathology-CH06 Heredity-89

University

89 Qs

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Quizizz 112-1 Pathology-CH06         Heredity-89

Quizizz 112-1 Pathology-CH06 Heredity-89

Assessment

Quiz

Biology

University

Medium

Created by

66 鍾雪玉

Used 3+ times

FREE Resource

89 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

10 sec • 1 pt

三核苷酸重複(trinucleotide repeat)擴增型突變所引起的遺傳疾病中,隨著後代代數的增加,臨床症狀逐漸加重,且發病時間逐漸提早,此現象稱為下列何者?(112-1專高)
anticipation
degeneration
deterioration
progression

2.

MULTIPLE CHOICE QUESTION

10 sec • 1 pt

有關先天性(congenital)疾病之敘述,下列何者最正確?(111-2專高)
均為顯性遺傳
都是出生時就發生
都是染色體突變造成
均會造成內臟器官結構改變

3.

MULTIPLE CHOICE QUESTION

10 sec • 1 pt

正常女性受精卵之染色體為: ('93專高)
23,X
23,Y
46,XY
46,XX。

4.

MULTIPLE CHOICE QUESTION

10 sec • 1 pt

染色體分析若為46,XX, t(2;5)(q31;p14)表示染色體有何種現象發生?('04專高)
染色體佚失(deletion) (
染色體反轉(inversion)
環狀染色體(ring chromosome)
染色體轉位(translocation)。

5.

MULTIPLE CHOICE QUESTION

10 sec • 1 pt

粒線體DNA突變所造成的疾病以何種方式遺傳?('04專高)
父系遺傳
母系遺傳
性聯遺傳
體染色體遺傳。

6.

MULTIPLE CHOICE QUESTION

10 sec • 1 pt

第八凝血因子基因變異最常見的是:(103-1專高醫分)
點突變
小段DNA缺失或嵌入
大段DNA缺失或嵌入
基因反轉異常

7.

MULTIPLE CHOICE QUESTION

10 sec • 1 pt

我國常見之乙型海洋性貧血基因 II-654型是屬於:(103-1專高醫分)
Promoter mutation
Nonsense mutation
Frameshift mutation
Splicing mutation

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