آزمایش FISH (Fluorescent in situ hybridization)
FISH آزمایش: آزمایش فیش شمارشی یک روش تخصصی ژنتیکی است که برای بررسی تعداد کروموزوم ھا یا نواحی ژنی
بهمن 20, 1404
نویسنده: novinad
دسته بندی نشده
آزمایش کاریوتیپ مغز استخوان
ﻣﻐﺰ اﺳﺘﺨﻮان ﺑﺎﻓﺘﯽ ﻧﺮم و اﺳﻔﻨﺠﯽ است ﮐه وظﯿﻔه ﺗﻮﻟﯿﺪ ﮔﻠﺒﻮلھﺎی ﻗﺮﻣﺰ، ﺳﻔﯿﺪ و سلول های ﭘﻼﮐﺖ را ﺑﺮ
بهمن 20, 1404
مقالات علمی
مقالات علمی آزمایشگاه نوین ژنتیک :
Report of an Iranian child with chronicabdominal pain and constipation diagnosedas glycogen storage disease type IX: a casereport Abstract
اردیبهشت 21, 1404
Haplotypes inside the beta-globin gene:use as new biomarkers for beta-thalassemiaprenatal diagnosis in north of Iran
Abstract :Background: Beta-thalassemia is common in the Mediterranean area as well as the Middle East and India. Official report
اردیبهشت 16, 1404
آزمایش ژنتیک انواع سرطان
سرطان تیروئید یکی از انواع سرطانهایی است که از غده تیروئید شروع میشود و انواع مختلفی دارد که به
اردیبهشت 16, 1404
Alpha‐globin gene mutation spectrum in patients withmicrocytic hypochromic anemia from Mazandaran Province, Iran
Abstract :Background: It is estimated about 7% of the world population is carriers of hemoglobin diseases. Alpha‐thalassemia is one
اردیبهشت 11, 1404
Laing Early-onset Distal Myopathy Due to the MYH7Mutation in an Iranian Family
Abstract :Introduction: Laing early-onset distal myopathy is a disorder with autosomal dominant inheritance pattern caused by a mutation in
اردیبهشت 11, 1404
GJB2 Gene Related Nonsyndromic Hearing Lossin Mazandaran Province, North of Iran
Abstract :Introduction: Congenital hearing loss is the most common sensory deficit in the world and mutations in GJB2 gene
اردیبهشت 11, 1404
Frequencies of CYP2B6∗4,∗5, and ∗6 Alleles within an IranianPopulation (Mazandaran)
Background: -e human CYP2B subfamily consists of one functional gene (CYP2B6) and one pseudogene (CYP2B7P). Cytochrome P450 2B6 (CYP2B6)
اردیبهشت 11, 1404
Frequency of PAH Mutations Among Classic Phenylketon Urea Patients in Mazandaran and Golestan Provinces, North of Iran
SUMMARY :Background: Phenylketonuria (PKU) is the most common aminoacidopathy with an autosomal recessive inheri-tance pattern. A global PKU prevalence
اردیبهشت 10, 1404