نتایج جستجو برای: cleidocranial syndrome
تعداد نتایج: 623409 فیلتر نتایج به سال:
Cleidocranial dysplasia (CCD), an autosomal dominant disorder with a prevalence of 1 in 1,000,000 individuals, is mainly caused by mutations in Runx2, a gene required for osteoblastic differentiation. It is generally characterized by hypoplastic clavicles, narrow thorax, and delayed or absent fontanel closure. Importantly, its orofacial manifestations, including midfacial hypoplasia, retained p...
چکیده ندارد.
Monoallelic RUNX1 mutations cause familial platelet disorder with predisposition for acute myelogenous leukemia (FPD/AML). Sporadic mono- and biallelic mutations are found at high frequencies in AML M0, in radiation-associated and therapy-related myelodysplastic syndrome and AML, and in isolated cases of AML M2, M5a, M3 relapse, and chronic myelogenous leukemia in blast phase. Mutations in RUNX...
This paper analyzes the dynamics of objective laser speckles as the distance between the object and the observation plane continuously changes. With the purpose of applying optical spatial filtering velocimetry to the speckle dynamics, in order to measure out-of-plane motion in real time, a rotational symmetric spatial filter is designed. The spatial filter converts the speckle dynamics into a ...
To cite: Vashisth P, Dwivedi S, Arora R, et al. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/ bcr-2013-008797 DESCRIPTION A 4-year-old boy was brought to the Department of Pedodontics and Preventive Dentistry with major tooth decay. An intraoral examination revealed the presence of a complete primary dentition, fair oral hygiene and the presence of double teeth in ...
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