5q35缺失,又称5号染色体单体型5q35,与Cornelia de Lange综合征1和双侧视神经发育不全有关。与5q35缺失有关的重要基因是NKX2-5(NK2同源盒5)。附属组织包括心脏。
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Deletion 5q35, also known as chromosome 5, monosomy 5q35, is related to cornelia de lange syndrome 1 and optic nerve hypoplasia, bilateral. An important gene associated with Deletion 5q35 is NKX2-5 (NK2 Homeobox 5). Affiliated tissues include heart.