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Non-Mendelian Genetics

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卡片总数: 16内容版本: v3公开卡包更新时间: 8/1/2026

卡片预览 (16 张)

#1
正面 (问题)

a form of intermediate inheritance where both alleles in the heterozygote express themselves equally

背面 (解答)

codominance

#2
正面 (问题)

neither allele expresses itself fully, therefore, there are no dominant or recessive alleles. it is nothing but a combined expression of the two alleles in the heterozygous condition producing a blend of the two individual phenotypes. (uppercase letters with superscripts are used)

背面 (解答)

incomplete dominance

#3
正面 (问题)

when there is a gene existing in more than two allelic forms (e.g. blood types and rabbit fur color)

背面 (解答)

multiple alleles

#4
正面 (问题)

a biological process that involves the transmission of traits or characters from parents to offspring

背面 (解答)

sex-linked inheritance

#5
正面 (问题)

caused by the variants in genes on the X chromosome, this is common in males because they have XY chromosomes. (e.g. hemophilia and color blindness)

背面 (解答)

X-linked recessive inheritance

#6
正面 (问题)

a rare, inherited blood disorder that occurs when the blood doesn’t clot properly because of the lack of Factor VIII is called?

背面 (解答)

Hemophilia

#7
正面 (问题)

a person cannot distinguish shades of red and green

背面 (解答)

red-green color blindness

#8
正面 (问题)

caused by the variants in genes on the X chromosome, this is common in males because they have XY chromosomes. (e.g. Rett Syndrome, Incontinentia pigmenti, and X-linked hypophosphatemic rickets (XLHR))

背面 (解答)

X-linked dominant inheritance

#9
正面 (问题)

causes physical and intellectual disability exclusively in females. symptoms include impairments in language and coordination and repetitive movements. those affected often have slower growth, difficulty walking, and a smaller head size.

背面 (解答)

Rett Syndrome

#10
正面 (问题)

is an inherited (genetic) condition that affects the skin and other systems in the body

背面 (解答)

Incontinentia pigmenti

#11
正面 (问题)

is characterized by hypophosphatemia, defective intestinal absorption of calcium, and rickets or osteomalacia unresponsive to vitamin D

背面 (解答)

X-linked hypophosphatemic rickets (XLHR)

#12
正面 (问题)

only happens if the altered gene that causes the disorder is located on the Y chromosome. it can only be passed from father to son because only males have a Y chromosome. (e.g. ear hypertrichosis, webbed toes, and porcupine man)

背面 (解答)

Y-linked inheritance

#13
正面 (问题)

is characterized by excessive body hair, especially on the ear

背面 (解答)

ear hypertrichosis

#14
正面 (问题)

is a web-like connection between the second and third toes

背面 (解答)

webbed toes

#15
正面 (问题)

occurs when the skin thickens and gradually becomes darker, scaly, rough, and with bristle-like outgrowths

背面 (解答)

porcupine man

#16
正面 (问题)

a chart that diagrams the inheritance of a trait or health condition through generations of a family

背面 (解答)

pedigree