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関連する概念動画

Sex-linked Disorders01:43

Sex-linked Disorders

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Like autosomes, sex chromosomes contain a variety of genes necessary for normal body function. When a mutation in one of these genes results in biological deficits, the disorder is considered sex-linked.
109.6K
Pleiotropy01:33

Pleiotropy

43.5K
Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause Waardenburg Syndrome Type 4, or WS4, which can cause defects in pigmentation, hearing impairments, and an absence of intestinal contractions necessary for elimination. This diversity of phenotypes results from the expression pattern of SOX10 in early embryonic and fetal development. SOX10 is found in neural crest cells that form melanocytes,...
43.5K
Karyotyping01:17

Karyotyping

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Overview
69.0K
Pedigree Analysis01:35

Pedigree Analysis

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Overview
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Genetic Lingo01:11

Genetic Lingo

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Overview
115.9K
Genomic Imprinting and Inheritance02:30

Genomic Imprinting and Inheritance

37.4K
Diploid organisms inherit genetic material through chromosomes from both parents. Copies of the same gene are known as alleles. In most cases, both alleles are simultaneously expressed and allow various cellular processes to function optimally. If one of the alleles is missing or mutated, the expression of the other allele can compensate; however, this is not true for all genes.
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
37.4K

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遺伝学. 遺伝学について. 1つの遺伝子 - 4つのシンドローム

V van Heyningen

    Nature
    |January 27, 1994
    PubMed
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    No abstract available in PubMed .

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