๐“๐“ฑ๐“ถ๐“ช๐“ญ ๐“๐“ต-๐“ฑ๐“ช๐“ป๐“ฝ๐“ฑ๐“ฒ

๐“๐“ฑ๐“ถ๐“ช๐“ญ ๐“๐“ต-๐“ฑ๐“ช๐“ป๐“ฝ๐“ฑ๐“ฒ

@lwaifi2122

ุญุณุงุจูŠ ุงู„ูˆุญูŠุฏ 1976 ๐Ÿงฌ ู†ุงุฏู†ูŠ ุจุงุณู…ูŠ ุฏูˆู† ุฃู† ูŠุณุจู‚ู‡ ุฏุงู„ ุฃูˆ ุฐุงู„ ุฃูˆ ุจุงุก ุฃูˆ ุฃู„ู ุฃูˆ ู„ู‚ุจ.

Riyadh ุงู†ุถู… Mar 2020
71
ุณู„ุงุณู„ ุงู„ุชุบุฑูŠุฏุงุช
487
ุนุฏุฏ ุงู„ู…ุดุงู‡ุฏุงุช
363
ู…ุชุงุจุนูˆู†
43.7K
ุชุบุฑูŠุฏุฉ

ุณู„ุงุณู„ ุงู„ุชุบุฑูŠุฏุงุช

ู‡ู„ ูŠู…ูƒู† ุฅู†ุชุงุฌ ุฃุฌู†ุฉ ู‡ุฌูŠู†ุฉ ู…ู† ู‚ุฑุฏ ูˆุฅู†ุณุงู† ููŠ ุงู„ู…ุฎุชุจุฑ! ุŸ (Human-monkey chimeric embryos) ุชู…ูƒู† ูุฑูŠู‚ ุจุญุซูŠ ุฏูˆู„ูŠ ู…ู† ุฅู†ุชุงุฌ ุฃุฌู†ุฉ ู‡ุฌูŠู†ุฉ ููŠ ู…ุฒุงุฑุน ุฎู„ูˆูŠุฉ (Ex vivo) ู…ู† ุฎู„ุงู„ ุฒุฑุน ุฎู„ุงูŠุง ุฌุฐุนูŠุฉ ุจุดุฑูŠุฉ...

ุงู„ู…ู‡ู‚ ุงู„ุฌู„ุฏูŠ ุงู„ุจุตุฑูŠ Oculocutaneous albinism ู‡ูˆ ู…ุฌู…ูˆุนุฉ ู…ู† ุงู„ุญุงู„ุงุช ุงู„ุชูŠ ุชุคุซุฑ ุนู„ู‰ ุชุตุจุบ ุงู„ุฌู„ุฏ ูˆุงู„ุดุนุฑ ูˆุงู„ุนูŠู†ูŠู†. ุนุงุฏุฉ ู…ุง ูŠูƒูˆู† ู„ุฏู‰ ุงู„ุฃูุฑุงุฏ ุงู„ู…ุชุฃุซุฑูŠู† ุจุดุฑุฉ ู†ุงุนู…ุฉ ุฌุฏุง ูˆุดุนุฑ ุฃุจูŠุถ ุฃูˆ ูุงุชุญ ุงู„ู„ูˆ...

ุญุงู„ุฉ ุชุนุฏุฏ ุงู„ุญุฏู‚ุงุช Polycoria ุชุนุชุจุฑ ุญุงู„ุฉ ุชุนุฏุฏ ุงู„ุญุฏู‚ุงุช ูˆุงุญุฏุฉ ู…ู† ุงู„ุฃู…ุฑุงุถ ุงู„ู†ุงุฏุฑุฉ ุงู„ุชูŠ ุชุตูŠุจ ุงู„ุนูŠู† ุจุญูŠุซ ูŠู…ุชู„ูƒ ุจุณุจุจู‡ุง ุงู„ู…ุฑูŠุถ ุนุฏุฉ ุญุฏู‚ุงุช ููŠ ุนูŠู† ูˆุงุญุฏุฉ. ููŠ ุญุงู„ุฉ ุชุนุฏุฏ ุงู„ุญุฏู‚ุงุช ุงู„ุญู‚ูŠู‚ูŠ ุชุชูุงุนู„...

(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. ๐ŸงฌPlasmids 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.

Hashimotoโ€™s disease ุฃุญุฏ ุฃู…ุฑุงุถ ุงู„ู…ู†ุงุนุฉ ุงู„ุฐุงุชูŠุฉ ูˆู‡ูˆ ู‚ุตูˆุฑ ููŠ ุงู„ุบุฏุฉ ุงู„ุฏุฑู‚ูŠุฉ ูˆ ู‡ุฐุง ุงู„ู…ุฑุถ ูŠุถุฑ ุจู‡ุง. ุงู„ุชุดุฎูŠุต ูˆ ุฅุฏุงุฑุฉ ู‡ุฐุง ุงู„ู…ุฑุถ ููŠู‡ุง ุตุนูˆุจุฉ ูˆุฑุจู…ุง ุชุทูˆู„ ุนู…ู„ูŠุฉ ุงู„ุชุดุฎูŠุต ู„ุฃุดู‡ุฑ.

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.

STOP SMOKING๐Ÿšญ https://t.co/EsyqrH3xB6

๐Ÿ‘๏ธWaardenburg #syndrome is a rare genetic condition that affects the color of a personโ€™s skin, hair, and eyes. It can also cause hearing loss. ๐Ÿ‘๏ธThere 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...