๐๐ฑ๐ถ๐ช๐ญ ๐๐ต-๐ฑ๐ช๐ป๐ฝ๐ฑ๐ฒ
ุญุณุงุจู ุงููุญูุฏ 1976 ๐งฌ ูุงุฏูู ุจุงุณู ู ุฏูู ุฃู ูุณุจูู ุฏุงู ุฃู ุฐุงู ุฃู ุจุงุก ุฃู ุฃูู ุฃู ููุจ.
ุนุฑุถ ูู ๐ุณูุงุณู ุงูุชุบุฑูุฏุงุช
ูู ูู ูู ุฅูุชุงุฌ ุฃุฌูุฉ ูุฌููุฉ ู ู ูุฑุฏ ูุฅูุณุงู ูู ุงูู ุฎุชุจุฑ! ุ (Human-monkey chimeric embryos) ุชู ูู ูุฑูู ุจุญุซู ุฏููู ู ู ุฅูุชุงุฌ ุฃุฌูุฉ ูุฌููุฉ ูู ู ุฒุงุฑุน ุฎูููุฉ (Ex vivo) ู ู ุฎูุงู ุฒุฑุน ุฎูุงูุง ุฌุฐุนูุฉ ุจุดุฑูุฉ...
ุงูู ูู ุงูุฌูุฏู ุงูุจุตุฑู Oculocutaneous albinism ูู ู ุฌู ูุนุฉ ู ู ุงูุญุงูุงุช ุงูุชู ุชุคุซุฑ ุนูู ุชุตุจุบ ุงูุฌูุฏ ูุงูุดุนุฑ ูุงูุนูููู. ุนุงุฏุฉ ู ุง ูููู ูุฏู ุงูุฃูุฑุงุฏ ุงูู ุชุฃุซุฑูู ุจุดุฑุฉ ูุงุนู ุฉ ุฌุฏุง ูุดุนุฑ ุฃุจูุถ ุฃู ูุงุชุญ ุงููู...
ุญุงูุฉ ุชุนุฏุฏ ุงูุญุฏูุงุช Polycoria ุชุนุชุจุฑ ุญุงูุฉ ุชุนุฏุฏ ุงูุญุฏูุงุช ูุงุญุฏุฉ ู ู ุงูุฃู ุฑุงุถ ุงููุงุฏุฑุฉ ุงูุชู ุชุตูุจ ุงูุนูู ุจุญูุซ ูู ุชูู ุจุณุจุจูุง ุงูู ุฑูุถ ุนุฏุฉ ุญุฏูุงุช ูู ุนูู ูุงุญุฏุฉ. ูู ุญุงูุฉ ุชุนุฏุฏ ุงูุญุฏูุงุช ุงูุญูููู ุชุชูุงุนู...
(Cushing's disease) When our body containsย excessiveย amount of cortisol for a long time, it causesย Cushing's disease. It is also known as hypercortisolism.
A plasmid is a small, circular DNA molecule that can replicate independently of chromosomal DNA. ๐งฌPlasmids almost always carry one or more genes. Often, the genes carried in plasm...
Kabuki #syndrome is a congenital mental retardation syndrome with additional features, including postnatal dwarfism.
Hashimotoโs disease ุฃุญุฏ ุฃู ุฑุงุถ ุงูู ูุงุนุฉ ุงูุฐุงุชูุฉ ููู ูุตูุฑ ูู ุงูุบุฏุฉ ุงูุฏุฑููุฉ ู ูุฐุง ุงูู ุฑุถ ูุถุฑ ุจูุง. ุงูุชุดุฎูุต ู ุฅุฏุงุฑุฉ ูุฐุง ุงูู ุฑุถ ูููุง ุตุนูุจุฉ ูุฑุจู ุง ุชุทูู ุนู ููุฉ ุงูุชุดุฎูุต ูุฃุดูุฑ.
DEFINITION: Mutations in the CHM gene cause choroideremia. INHERITANCE: X-linked dominant
Mutations in the CASK gene on X chromosome cause FG #syndrome-4 and intellectual developmental disorder with microcephaly and pontine and cerebellar hypoplasia.
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๐๏ธWaardenburg #syndrome is a rare genetic condition that affects the color of a personโs skin, hair, and eyes. It can also cause hearing loss. ๐๏ธThere are four main types of Waard...
Heterozygous mutations in the SF3B4 gene cause Nager type of acrofacial dysostosis, which is the typical form of a group of disorders collectively known as the acrofacial dysostose...