نتایج جستجو برای: fam83h

تعداد نتایج: 59  

Journal: :iranian journal of public health 0
s jalal pourhashemi dept. of pediatric dentistry, tehran university of medical sciences, tehran, iran ; dept. of pediatric dentistry, tehran university of medical sciences, international campus, tehran, iran. mehdi ghandehari motlagh dept. of pediatric dentistry, tehran university of medical sciences, tehran, iran. ghasem meighani dept. of pediatric dentistry, tehran university of medical sciences, tehran, iran. azadeh ebrahimi takaloo dept. of pediatric dentistry, tehran university of medical sciences, tehran, iran. mahsa mansouri dept. of pediatric dentistry, tehran university of medical sciences, tehran, iran. fatemeh mohandes dept. of pediatric dentistry, tehran university of medical sciences, tehran, iran.

amelogenesis imperfecta (ai) is a disorder of tooth development where there is an abnormal formation of enamel or the external layer of teeth. the aim of this study was to screen mutations in the four most important candidate genes, enam, klk4, mmp20 and fam83h responsible for amelogenesis imperfect.geneomic dna was isolated from five iranian families with 22 members affected with enamel malfor...

Journal: :Molecular Genetics & Genomic Medicine 2019

Journal: :journal of sciences, islamic republic of iran 2011
mansour heidari

amelogenesis imperfectas (ais) are clinically and genetically heterogeneous conditions characterized by a wide range of clinical features. these abnormalities of enamel formation are categorized into three main groups, hypoplastic, hypomaturation and hypocalcified with different modes of inheritance such as autosomal recessive (ar), autosomal dominant (ad) and x-lined recessive (xlr). in spite ...

Journal: :Molecular Genetics & Genomic Medicine 2015

2012
Oliver P. Forman Jacques Penderis Claudia Hartley Louisa J. Hayward Sally L. Ricketts Cathryn S. Mellersh

The domestic dog (Canis familiaris) segregates more naturally-occurring diseases and phenotypic variation than any other species and has become established as an unparalled model with which to study the genetics of inherited traits. We used a genome-wide association study (GWAS) and targeted resequencing of DNA from just five dogs to simultaneously map and identify mutations for two distinct in...

Mansour Heidari

Amelogenesis Imperfectas (AIs) are clinically and genetically heterogeneous conditions characterized by a wide range of clinical features. These abnormalities of enamel formation are categorized into three main groups, hypoplastic, hypomaturation and hypocalcified with different modes of inheritance such as autosomal recessive (AR), autosomal dominant (AD) and X-lined recessive (XLR). In spite ...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید