英文字典中文字典


英文字典中文字典51ZiDian.com



中文字典辞典   英文字典 a   b   c   d   e   f   g   h   i   j   k   l   m   n   o   p   q   r   s   t   u   v   w   x   y   z       







请输入英文单字，中文词皆可：

dramatically    音标拼音: [drəm'ætɪkli] [drəm'ætɪkəli]
ad. 从戏剧角度;戏剧性地,显著地

从戏剧角度;戏剧性地,显着地

安装中文字典英文字典查询工具!


中文字典英文字典工具:
选择颜色:
输入中英文单字

































































英文字典中文字典相关资料:


  • Waardenburg syndrome - Wikipedia
    Waardenburg syndrome is a group of rare genetic conditions characterised by at least some degree of congenital hearing loss and pigmentation deficiencies, which can include bright blue eyes (or one blue eye and one brown eye), a white forelock or patches of light skin
  • Waardenburg Syndrome: Symptoms Causes - Cleveland Clinic
    Waardenburg syndrome is a genetic condition that causes changes to the coloring (pigmentation) of your hair, eyes and skin and can cause hearing loss in some people
  • Waardenburg syndrome | About the Disease | GARD
    Waardenburg syndrome (WS) is a group of genetic conditions characterized by varying degrees of hearing loss and differences in the coloring (pigmentation) of the eyes, hair, and skin Signs and symptoms can vary both within and between families Various other features may also be present
  • Waardenburg Syndrome - Symptoms, Causes, Treatment | NORD
    Waardenburg syndrome (WS) is a group of genetic disorders present at birth that affect hair, skin, and eye color and may cause hearing loss
  • What Should You Know About Waardenburg Syndrome? - WebMD
    Waardenburg syndrome is a genetic condition that affects the color of your hair, skin, and eyes and can also cause hearing loss and gastrointestinal issues There's no cure, but your doctor can
  • Waardenburg Syndrome: What Is It, Causes, Diagnosis, and More | Osmosis
    Waardenburg syndrome is a rare congenital disease involving a group of genetic conditions, including distinctive facial features, discoloration of various body parts, and congenital hearing loss
  • Waardenburg syndrome - Orphanet
    WS accounts for 2-5% of congenital hearing loss and affects all ethnic groups without gender differences WS2 is the most common subtype, followed by WS1 Clinical manifestations vary within and between families
  • Waardenburg syndrome - DermNet
    Waardenburg syndrome is a neurocristopathy due to gene mutations which result in abnormal neural crest differentiation during embryonic development Mutations in a number of different genes can cause Waardenburg syndrome, with some differences in symptoms and signs
  • Waardenburg syndrome: MedlinePlus Genetics
    Waardenburg syndrome is a group of genetic conditions that can cause hearing loss and changes in coloring (pigmentation) of the hair, skin, and eyes Although most people with Waardenburg syndrome have normal hearing, moderate to profound hearing loss can occur in one or both ears
  • Clinical Insights Into Waardenburg-Shah Syndrome: A Case Series and . . .
    Waardenburg-Shah syndrome is an autosomal recessive disorder with mutations identified in the sex-determining region Y (SRY) box 10 (SOX10), endothelin-3 (EDN3), or its receptor endothelin receptor type B (EDNRB) genes, which play a vital role in neural crest cell migration





中文字典-英文字典  2005-2009