翻訳と辞書
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・ Chromosomal deletion syndrome
・ Chromosomal fragile site
・ Chromosomal inversion
・ Chromosomal polymorphism
・ Chromosomal rearrangement
・ Chromosomal translocation
・ Chromosome
・ Chromosome (genetic algorithm)
・ Chromosome 1 (human)
・ Chromosome 10 (human)
・ Chromosome 11 (human)
・ Chromosome 12 (human)
・ Chromosome 13 (human)
・ Chromosome 14 (human)
・ Chromosome 15 (human)
Chromosome 15q partial deletion
・ Chromosome 15q trisomy
・ Chromosome 16 (human)
・ Chromosome 16 open reading frame 13
・ Chromosome 17 (human)
・ Chromosome 18 (human)
・ Chromosome 19 (human)
・ Chromosome 2 (human)
・ Chromosome 20 (human)
・ Chromosome 21 (human)
・ Chromosome 22 (human)
・ Chromosome 3 (human)
・ Chromosome 4 (human)
・ Chromosome 5 (human)
・ Chromosome 5q deletion syndrome


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Chromosome 15q partial deletion : ウィキペディア英語版
Chromosome 15q partial deletion

Chromosome 15q partial deletion is an extremely rare human genetic disorder, caused by a chromosomal aberration in which the long ("q") arm of one copy of chromosome 15 is deleted, or partially deleted. If the mother's copy of the chromosomal arm is deleted, Angelman syndrome results. If the father's copy of the chromosomal arm is deleted, Prader-Willi syndrome results. The smallest observed region that can result in these syndromes when deleted is therefore called the PWS/AS critical region and is situated at 15q11-q13. In addition to deletions, uniparental disomy of chromosome 15 gives rise to the same genetic disorders, indicating that genomic imprinting must occur in this region.
==See also==

*Chromosome 15q trisomy
*Genetics
*Genetic deletion


抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
ウィキペディアで「Chromosome 15q partial deletion」の詳細全文を読む



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