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Titlebook: Radiology of the Hand; A Diagnostic Synopsi Cornelis J. P. Thijn Book 1986 Springer-Verlag Berlin Heidelberg 1986 Tumor.aneurysm.bone.diagn

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發(fā)表于 2025-3-21 18:49:46 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Radiology of the Hand
副標(biāo)題A Diagnostic Synopsi
編輯Cornelis J. P. Thijn
視頻videohttp://file.papertrans.cn/821/820852/820852.mp4
圖書封面Titlebook: Radiology of the Hand; A Diagnostic Synopsi Cornelis J. P. Thijn Book 1986 Springer-Verlag Berlin Heidelberg 1986 Tumor.aneurysm.bone.diagn
出版日期Book 1986
關(guān)鍵詞Tumor; aneurysm; bone; diagnosis; differential diagnosis; diseases; evaluation; growth; hand; radiology; skele
版次1
doihttps://doi.org/10.1007/978-3-642-50966-7
isbn_softcover978-3-642-50968-1
isbn_ebook978-3-642-50966-7
copyrightSpringer-Verlag Berlin Heidelberg 1986
The information of publication is updating

書目名稱Radiology of the Hand影響因子(影響力)




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沙發(fā)
發(fā)表于 2025-3-21 20:55:05 | 只看該作者
Primary Growth Disturbances,uent eyebrows, small upturned nose, micrognathia, wide and down-turned upper lip), delayed skeletal maturation, and small hands and feet. Cutaneous syndactyly of the feet, proximal insertion of the thumbs, and clinodactyly are often present. In severe cases, any of the upper extremity bones can be a
板凳
發(fā)表于 2025-3-22 01:27:00 | 只看該作者
Other Disorders of Bones and Joints,us contractures, and joint ankylosis. On autopsy, a decrease in the size of the spinal cord, a decreased number of anterior horn cells, and signs of motor demyelinization are found [1]. In some cases autosomal recessive inheritance is likely, but most cases are sporadic. The clinical picture is char
地板
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Osteochondrodysplasias,The most obvious clinical features of this sporadically occurring disorder are shortened limbs, a normal-sized trunk, a narrow thorax, a large head with a prominent forehead, and a protuberant abdomen. The affected infants are still-born or die of respiratory failure within hours or days after birth.
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發(fā)表于 2025-3-22 23:28:08 | 只看該作者
Chromosomal Aberrations,After mongolism, trisomy 18 is the second most common syndrome of multiple abnormalities [1]. It is usually caused by a full trisomy of the number 18 chromosome. A large variety of abnormalities may be found [1–3].
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