常染色体隐性遗传的英文

• ar autosome recessive
• autosomal recessive inheritance, ar
• autosome recessive inheritance

• "常染色体"英文翻译    autosome; euchromosome
• "隐性遗传"英文翻译    recessive inheritance
• "常染色体隐性遗传病" 英文翻译 :    autosomal recessive inherited disease; autosome recessive disease
• "常染色体隐性遗传特性" 英文翻译 :    autosomal recessive trait
• "常染色体隐性遗传性聋" 英文翻译 :    autosomal recessive hereditary deafness
• "为常染色体隐性遗传病" 英文翻译 :    type b sanfilippo syndrome
• "常染色体隐性遗传氨酰脯基氨酸酶缺乏" 英文翻译 :    autosomal recessive prolidase deficiency
• "常染色体隐性遗传性征不发育侏儒症" 英文翻译 :    autosomal recessive asexual dwarfism
• "常染色体隐性遗传眼白化病" 英文翻译 :    autosomal recessive ocular albimism; autosomal recessive ocular albinism
• "一种常染色体隐性遗传综合征" 英文翻译 :    baller-gerold syndrome
• "常染色体隐性" 英文翻译 :    autosomal recessive
• "常染色体隐性基因" 英文翻译 :    autosomal recessive gene
• "常染色体隐性致死" 英文翻译 :    autosomal recessive lethal
• "常染色体隐形遗传" 英文翻译 :    autosomal recessive inheritance
• "常染色体显性遗传" 英文翻译 :    ad autosomal dominant inheritance; autosomal dominant inheritance, ad; autosomal dominant transmission; autosome dominant inheritance
• "常染色体隐性维生素d依赖" 英文翻译 :    autosomal recessive vitamin d dependency
• "常染色体显性遗传病" 英文翻译 :    autosomal dominant inherited disease
• "常染色体显性遗传疾病" 英文翻译 :    autosome dominant disease
• "限性常染色体显性遗传" 英文翻译 :    sex-limited autosomal dominant inheritance
• "限性常染色体显性遗传病" 英文翻译 :    sex-limited-autosomal dominant genetic disorder; sex-limited-autosomal dominant genitic disorder
• "性限常染色体显性遗传" 英文翻译 :    sex-limited autosomal dominant inheritance
• "常染色体隐性先天性鱼鳞病" 英文翻译 :    arci
• "常染色体隐性型低丙种球蛋白血症" 英文翻译 :    autosomal recessive type hypogammaglobulinemia
• "常染色体隐性婴儿多囊肾疾病" 英文翻译 :    autosomal recessive infantile polycystic kidney disease
• "常染色体隐性肢带肌营养不良" 英文翻译 :    autosomal recessive limb-girdle muscular dystrophy

• Autosomal recessive inheritance , ar
  常染色体隐性遗传
• Consider as what recessive heredity causes euchromosome to high myopia
  对于高度近视则认为是常染色体隐性遗传引起的。
• Complex vertebral malformation ( cvm ) , a lethal autosomal recessive inherited defect in holstein breed , was newly reported in demark
  摘要荷斯坦奶牛脊柱畸形综合征是近年新发现的一种常染色体隐性遗传病，该病对纯合子胎儿是致死性的。
• In the autosomal recessive condition , the parents are generally healthy ? we call them ‘ carriers . ’ the probability of them having a child with another affected child is 25 percent
  对于常染色体隐性遗传，父母表面上通常是正常的? ?我们称之为“携带者” 。他们生育相同疾病小孩的几率将是25 % 。
• Hemochromatosis can be primary ( the cause is probably an autosomal recessive genetic disease ) or secondary ( excess iron intake or absorption , liver disease , or numerous transfusions )
  血色素沉着症或可以是原发的（病因大概为常染色体隐性遗传病） ，也可以是继发的（过多的铁摄取或吸收、肝脏疾病、大量输血） 。
• Wilson " s disease is the consequence of toxic accumulation of copper initially in the liver and later in extrahepatic sites , this disorder is inherited in autosomal recessive manner and is present in 1 in 30000 individuals in all populations
  其中研究最多的是铜代谢异常所引起的wilson ' s病，这种病是常染色体隐性遗传病，如果肝脏中铜浓度达到毒性水平，将引发急性肝炎，其发生率为三万分之一。