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"silent mutation"¿¡ ´ëÇÑ °Ë»ö °á°úÀÔ´Ï´Ù. °Ë»ö °á°ú º¸´Â µµÁß¿¡ Tab ۸¦ ´©¸£½Ã¸é °Ë»ö âÀÌ ¼±Åõ˴ϴÙ.
¾Ë±â½¬¿î ÀÇÇпë¾îÇ®ÀÌÁý, ¼­¿ïÀÇ´ë ±³¼ö ÁöÁ¦±Ù, °í·ÁÀÇÇÐ ÃâÆÇ À¯»ç °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
¿µ¹® mutation ÇÑ±Û µ¹¿¬º¯ÀÌ
¼³¸í   
  ¼¼Æ÷ÀÇ dna ÀÚüÀÇ º¯ÀÌ¿¡ ÀÇÇØ ÀϾ´Â ¼¼Æ÷º¯À̸¦ ¸»ÇÑ´Ù. ÀÌ·¯ÇÑ °æ¿ì µ¹¿¬º¯À̷ΠÀϾ ¼¼Æ÷´Â ±× ÀÌÈÄ µþ¼¼Æ÷(daughter cell)¿¡¼­µµ ±× º¯À̰¡ ¿©ÀüÈ÷ À¯ÁöµÇ¹Ç·Î Á¾(species)ÀÇ º¯È­³ª, È¤Àº ¼¼Æ÷ÀÇ ¾Ç¼ºº¯È¯(malignant transformation)¿¡ °ü¿©ÇÑ´Ù.
´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • siderophilin silent precordium
    ½Ãµ¥·ÎÇʸ°¹«Áõ»ó¾Õ°¡½¿
  • silent carrier
    ¹«Áõ»óº¸ÀÎÀÚ
  • silent gap
    ¹«À½°£°Ý
  • silent infection
    ¹«Áõ»ó°¨¿°
  • silent mastoiditis
    ¹«Áõ»ó²ÀÁöµ¹±â¿°, ÀẹÀ¯µ¹¿°
  • silent myocardial infarction
    ¹«Áõ»ó½É±Ù°æ»öÁõ
  • silent otitis media
    ¹«Áõ»óÁßÀÌ¿°
  • silent period
    ¹«Áõ»ó±â
  • silent prostatism
    ¹«Áõ»óÀü¸³»ùÁõ, ¹«Áõ»óÀü¸³¼±Áõ
  • silent receptor
    ¹«¹ÝÀÀ¼ö¿ëü
  • silent stone
    ¹«Áõ»óµ¹, ¹«Áõ»ó°á¼®
  • silent ulcer
    ¹«Áõ»ó±Ë¾ç
  • allelic mutation
    ¸Â¼¶µ¹¿¬º¯ÀÌ, ´ë¸³µ¹¿¬º¯ÀÌ
  • back mutation
    ¿ªµ¹¿¬º¯ÀÌ, º¹±Íµ¹¿¬º¯ÀÌ
  • cold-sensitive mutation
    Àú¿Â¹Î°¨µ¹¿¬º¯ÀÌ, Àú¿Â°¨¼ö¼ºµ¹¿¬º¯ÀÌ
´ëÇÑÀÇÇù Çʼö ÀÇÇпë¾îÁý »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 7 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • silent period
    ¹«Áõ»ó±â
  • silent ulcer
    ¹«Áõ»ó±Ë¾ç
  • mutation
    µ¹¿¬º¯ÀÌ
  • point mutation
    Á¡µ¹¿¬º¯ÀÌ
  • reverse mutation
    ¿ªµ¹¿¬º¯ÀÌ, º¹±Íµ¹¿¬º¯ÀÌ
  • somatic mutation
    ü¼¼Æ÷µ¹¿¬º¯ÀÌ
  • mutation rate
    µ¹¿¬º¯ÀÌÀ²
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • silent carrier
    ¹«Áõ»óº¸ÀÎÀÚ
  • silent electrode
    ¹«°üÀü±Ø
  • silent gap
    ¹«À½°£°Ý
  • silent infection
    ¹«Áõ»ó°¨¿°
  • silent myocardial infarction
    ¹«Áõ»ó½É±Ù°æ»öÁõ
  • silent mastoiditis
    ¹«Áõ»ó²ÀÁö¿°, Àẹ²ÀÁö¿°
  • silent otitis
    media ¹«Áõ»óÁßÀÌ¿°
  • siderophilin silent precordium
    ½Ãµ¥·ÎÇʸ°¹«Áõ»ó¾Õ°¡½¿
  • silent period
    ¹«Áõ»ó±â, ¹«¹ÝÀÀ±â
  • silent prostatism
    ¹«Áõ»óÀü¸³»ùÁõ
  • silent receptor
    ¹«¹ÝÀÀ¼ö¿ëü
  • silent otitis media
    ¹«Áõ»óÁßÀÌ¿°
  • silent stone
    ¹«Áõ»óµ¹
  • silent suicide
    Ä¡·á°ÅºÎÀÚ»ì
  • silent ulcer
    ¹«Áõ»ó±Ë¾ç
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 13 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • persistent silent infection
    Áö¼Ó¼º Àẹ°¨¿°.
  • frameshift mutation
    ÇØµ¶Æ² µ¹¿¬º¯ÀÌ, ÇÁ·¹ÀÓ½¬ÇÁÆ® µ¹¿¬º¯ÀÌ
  • genetic mutation
    À¯ÀüÀû µ¹¿¬º¯ÀÌ
  • genomic mutation
    À¯ÀüÀÚµ¹¿¬º¯ÀÌ
  • induced mutation
    À¯¹ßµ¹¿¬º¯ÀÌ
  • induced mutation
    À¯¹ß¼º µ¹¿¬º¯ÀÌ.
  • plaque morphology mutation
    ÇöóÅ© ÇüÅ µ¹¿¬º¯ÀÌ
  • plaque-type mutation
    ÇöóÅ©Çü µ¹¿¬º¯ÀÌ
  • point mutation
    Á¡ µ¹¿¬º¯ÀÌ
  • point mutation
    Á¡µ¹¿¬º¯ÀÌ
  • population mutation
    Áý´Ü±ºµ¹¿¬º¯ÀÌ(¡­ÔÍæÔܨì¶).
  • recessive mutation
    ¿­¼ºµ¹¿¬º¯ÀÌ(æëàõÔÍæÔܨì¶).
  • recessive mutation
    ¿­¼ºµ¹¿¬º¯ÀÌ
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • otitis media, silent
    ¹«Áõ»óÁßÀÌ¿°, Àẹ(¼º) ÁßÀÌ¿°
  • persistent silent infection
    Áö¼Ó¼º Àẹ°¨¿°.
  • siderophilin silent precordium
  • silent aneurysm
    ¹«Áõ»óµ¿¸Æ·ù(¡­ÔÑØæ×»).
  • silent aneurysm
    ¹«Áõ»óµ¿¸Æ·ù(¡­ÔÑØæ×»)
  • silent area
    ħ¹¬¾ß( Ùùå¯).
  • silent area
    ħ¹¬¾ß(öØÙùå¯)
  • silent carrier
    ¹«Áõ»óº¸ÀÎÀÚ
  • silent discharge
    ¹«°ü¹æÀü(¡­Û¯ï³).
  • silent displacement
    ħ¹¬ ÀüÀ§
  • silent electrode
    ¹«°üÀü±Ø(Ùíηï³Ð¿).
  • silent gap
    ¹«À½°£°Ý(ÙíëåÊà̰).
  • silent gap
    ¹«À½°£°Ý(ÙíëåÊà̰)
  • silent infection =subclinical i.
    ¹«Áõ»ó°¨¿°(ÙíñøßÒÊïæø).
  • silent infection =subclinical i.
    ¹«Áõ»ó°¨¿°(ÙíñøßÒÊïæø)
´ëÇÑÇØºÎÇÐȸ ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • Genomic mutation
    À¯ÀüÀÚµ¹¿¬º¯ÀÌ
    [¿¾ ¿ë¾î] À¯ÀüÀÚµ¹¿¬º¯ÀÌ
´ëÇÑ»ýÈ­ÇкÐÀÚ»ý¹°ÇÐȸ ¿ë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • silent mutation
    ħ¹¬ º¯ÀÌ(öØÙùܨì¶)
´ëÇÑ»ýÈ­ÇкÐÀÚ»ý¹°ÇÐȸ ¿ë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • silent allele
    ħ¹¬ ´ë¸³À¯ÀüÀÚ(öØÙùÓߨ¡ë¶îîí­)
  • silent gene
    ħ¹¬ À¯ÀüÀÚ(öØÙùë¶îîí­)
  • anucleolate mutation
    ¹«ÇÙÀÎ º¯ÀÌ(Ùíú·ìÝܨì¶)
  • back mutation
    º¹±Íº¯ÀÌ(ÜÖÏýܨì¶)
  • chain termination mutation
    »ç½½Çü¼º(û¡à÷) Á¾·á(ðûÖõ) º¯ÀÌ(ܨì¶)
  • constitutive mutation
    ±¸¼ºº¯ÀÌ(ϰà÷ܨì¶)
  • copy-error mutation
    º¹»ç¿À·ù º¯ÀÌ(ÜÜÞÐè¦×½Ü¨ì¶)
  • down promoter mutation
    ÇÏÇâÃËÁøÀÚ º¯ÀÌ(ù»ú¾õµòäí­Ü¨ì¶) (ÔÒ) promoter down mutation
  • end-point mutation
    Á¾¸»Á¡ º¯ÀÌ (ðûØÇïÇܨì¶)
  • forward mutation
    ³ªÅ¸³² º¯ÀÌ(ܨì¶)
  • frameshift mutation
    ƲÀ̵¿(ì¹ÔÑ) º¯ÀÌ(ܨì¶)
  • germinal mutation
    ¹è¼¼Æ÷ º¯ÀÌ(ÛÏá¬øàܨì¶)
  • induced mutation
    À¯µµº¯ÀÌ(ë¯Óôܨì¶)
  • intergenic suppressor mutation
    À¯ÀüÀÚ°£ ¾ï¾ÐÀÚº¯ÀÌ(ë¶îîí­Êàåääâí­Ü¨ì¶)
  • intragenic suppression mutation
    À¯ÀüÀÚ³» ¾ï¾Ðº¯ÀÌ(ë¶îîí­Ò®åääâܨì¶)
KI ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 4 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • mutation
    µ¹¿¬ º¯ÀÌ
  • silent displacement
    ħ¹¬ÀüÀ§
  • silent infection
    ¹«Áõ»ó°¨¿°
  • silent stone
    ¹«Áõ»ó°á¼®, Àẹ¼º°á¼®
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
SMI Self-Motivation Inventory; senior medical investigator; severe mental impairment; silent myocardial ...
SP sacroposterior; sacrum to pubis; salivary progesterone; schizotypal personality; semi-private [room]...
ARMS adverse reaction monitoring system; amplification refractory mutation system
MF magnetic field; meat free; medium frequency; megafarad; membrane filler; merthiolate-formaldehyde [s...
TFM testicular feminization male; testicular feminization mutation; total fluid movement; transmission e...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
SMI Silent myocardial ischemia
SIR Silent Information Regulator
SP Silent Period
SCI Silent cerebral infarction
SI Silent myocardial ischaemia
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü ¸ÂÃã °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • silent mutation
    ¹«ÁõÈÄ µ¹¿¬º¯ÀÌ
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • masticatory muscle silent
    ÀúÀÛ±ÙÀÇ ÈÞÁö±â
  • silent
    ¹«Áõ»óÀÇ, ¹«ÁõÈÄÀÇ, ¹«À½ÀÇ, ħ¹¬ÀÇ, ÀáÀ缺ÀÇ
    ¹ß°ßÇÒ ¼ö Àִ ¡ÈÄ ¶Ç´Â Áõ»óÀÌ ¾ø´Â, ¼Ò¸®°¡ ¾ø´Â.
  • silent displacement
    ħ¹¬ ÀüÀ§
  • silent period
    ħ¹¬±â, È޽ıâ, ¹«Áõ»ó±â, ÈÞÁö±â
    »ý¹°ÀÇ ¼¼Æ÷°¡ ±â´ÉÀûÀ¸·Î´Â Ȱµ¿À» Çϰí ÀÖÀ¸³ª, ÇÙ ºÐ¿­À̳ª ¼¼Æ÷ ºÐ¿­À» Çϰí ÀÖÁö ¾Ê´Â ½Ã±â.
  • silent stone
    ¹«Áõ»ó °á¼®, Àẹ¼º °á¼®
  • amber mutation
    ¾Ïº£¸£ µ¹¿¬º¯ÀÌ
  • auxotrophic mutation
    ¿µ¾ç ¿ä±¸ µ¹¿¬º¯ÀÌ
  • biochemical mutation
    »ýÈ­ÇÐÀû µ¹¿¬º¯ÀÌ
  • clear plaque mutation
    Åõ¸í ÇöóÅ© µ¹¿¬º¯ÀÌ
  • cold-sensitive mutation
    ÇÑ·© ¹Î°¨¼º µ¹¿¬º¯ÀÌ
  • conditional mutation
    Á¶°ÇºÎ µ¹¿¬º¯ÀÌ
  • constitutive mutation
    ±¸¼ºÀû µ¹¿¬º¯ÀÌ
  • frameshift mutation
    °ñ°Ý ±¸Á¶ À̵¿ µ¹¿¬º¯ÀÌ
  • homoetic mutation
    È£¸Þ¿À½Ã½º µ¹¿¬º¯ÀÌ
  • missense mutation
    ¹Ì½º¼¾½º µ¹¿¬º¯ÀÌ
CancerWEB ¿µ¿µ ÀÇÇлçÀü ¸ÂÃã °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
silent mutation Mutations that have no effect on phenotype because they do not affect the activity of the product of the gene, usually because of codon ambiguity.
(18 Nov 1997)
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
masticatory silent period A pause in electromyographic patterns associated with tooth contacts during chewing and biting; a part of the complex feedback mechanism of mandibular control involving receptors in the periodontal ligament and muscles.
(05 Mar 2000)
silent Producing no detectable signs or symptoms, said of certain diseases or morbid processes.
(05 Mar 2000)
silent allele 1. <genetics> A gene which is inactive. Thus, an amorphic gene.
2. <cell biology> Something that lacks a discernible shape and thus can be describes as amorphous.
(05 Feb 1998)
silent area Any area of the cerebrum or cerebellum in which lesions cause no definite sensory or motor symptoms.
(05 Mar 2000)
silent electrode In unipolar electrocardiography, a remote electrode placed either upon a single limb or connected with the central terminal and paired with an exploring electrode; the indifferent electrode is supposed to contribute little or nothing to the resulting record.
Synonym: dispersing electrode, silent electrode.
(05 Mar 2000)
silent gap The period during which Korotkoff sounds indicating true systolic pressure fade away and reappear at a lower pressure point; responsible for errors made in recording falsely low systolic blood pressure, especially in hypertensive patients, of up to 25 mm Hg, and avoided by pumping the cuff 30 mm Hg beyond palpable systolic pressure.
Synonym: silent gap.
(05 Mar 2000)
silent ischemia Myocardial ischemia without accompanying signs or symptoms of angina pectoris; can be detected by EKG and other lab techniques.
See: silent myocardial infarction.
(05 Mar 2000)
silent mutant A mutant that is not phenotypically manifest.
Synonym: silent mutant.
(05 Mar 2000)
silent myocardial infarction Infarction that produces none of the characteristic symptoms and signs of myocardial infarction.
(05 Mar 2000)
silent period The time during which there is no electrical activity in a muscle following its rapid unloading, any pause in an otherwise continuous series of electrophysiologic events.
(05 Mar 2000)
acquired mutation A change in a gene or chromosome that occurs in a single cell after the conception of the individual. That change is then passed along to all cells descended from that cell. Acquired mutations are involved in the development of cancer.
(12 Dec 1998)
addition-deletion mutation <molecular biology> A type of mutation that results from insertion or deletion of a single nucleotide into, or from, an open reading frame in the normal DNA sequence.
Normally, the genetic code is read in the wrong frame, three nucleotides at a time, and the entire sequence downstream of the mutation, is translated into a polypeptide with a garbled amino acid sequence from the mutated codon onwards. These mutations may be induced by certain types of mutagens or may occur spontaneously and usually result in the generation, downstream, of nonsense, chain termination codons.
Synonym: addition mutation, addition-deletion mutation, deletion mutation, reading-frameshift mutation.
(21 Jun 2000)
addition mutation <molecular biology> A type of mutation that results from insertion or deletion of a single nucleotide into, or from, an open reading frame in the normal DNA sequence.
Normally, the genetic code is read in the wrong frame, three nucleotides at a time, and the entire sequence downstream of the mutation, is translated into a polypeptide with a garbled amino acid sequence from the mutated codon onwards. These mutations may be induced by certain types of mutagens or may occur spontaneously and usually result in the generation, downstream, of nonsense, chain termination codons.
Synonym: addition mutation, addition-deletion mutation, deletion mutation, reading-frameshift mutation.
(21 Jun 2000)
amber mutation <molecular biology> A mutation from a codon which codes for an amino acid into the amber codon UAG, which normally signals that the translation of mRNA into an amino acid chain should stop.
The mutation causes the amino acid chain to stop forming before it is actually completed.
(09 Oct 1997)
back mutation <molecular biology> A mutation that causes a mutant gene to revert to its original wild-type base sequence.
Compare: forward mutation.
(09 Oct 1997)
KMLE À¥ ¿ë¾î ¸ÂÃã °Ë»ö °á°ú : 4 ÆäÀÌÁö: 1
silent mutation A mutation in a codon that does not cause a change in the amino acid sequence of the translation product.
Ãâó: www.genpromag.com/Glossary~LETTER~S.html
silent mutation Mutation that results in an unchanged amino acid sequence and thus in a protein with normal function.
Ãâó: science.education.nih.gov/supplements/nih1/genetic...
silent mutation a change in the genetic sequence that does not alter the protein sequence.
Ãâó: www.uvm.edu/~cgep/Education/Glossary.html
silent mutation Mutation in which the function of the protein product of the gene is unaltered.
Ãâó: depts.washington.edu/~genetics/courses/genet372/w2...
ÇÑ¿µ/¿µÇÑ »çÀü À¯»ç °Ë»ö °á°ú : 9 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • silent
    ħ¹¬ÀÇ
  • silent
    ħ¹¬ÇÏ´Â;Á¶¿ëÇÑ;¹«¾ðÀÇ;Á¶¿ëÇÑ;Ȱµ¿ÇÏÁö ¾Ê´Â;À͸íÀÇ;¹¬À½ÀÇ;¹«¾ðÀ¸·Î;ÀáÀÚÄÚ;Á¶¿ëÈ÷
  • mutation
    º¯°æ
  • forward mutation
    ÀüÁø µ¹¿¬ º¯ÀÌ
  • frameshift mutation
    ÇÁ·¹ÀÓ½ÃÇÁÆ® µ¹¿¬ º¯ÀÌ
  • missense mutation
    ¹Ì½º¼¾½º µ¹¿¬ º¯ÀÌ
  • mutation
    º¯È­;µ¹¿¬ º¯ÀÌ;º¯Á¾;¸ðÀ½ º¯È­
  • neutral mutation
    Á߸³µ¹¿¬º¯ÀÌ
  • vowel mutation
    =UMLAUT
ÀÌ ¾Æ·¡ ºÎÅÍ´Â °á°ú°¡ ¾ø½À´Ï´Ù.
KMLE ¾àǰ/ÀǾàǰ ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 1
  • Á¦Ç°¸í
    ¼ººÐ/ÇÔ·®
    ±¸ºÐ/º¸Çè±Þ¿©
KMLE ¾àǰ/ÀǾàǰ À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 1
  • Á¦Ç°¸í
    ¼ººÐ/ÇÔ·®
    ±¸ºÐ/º¸Çè±Þ¿©
¾Ë±â½¬¿î ÀÇÇпë¾îÇ®ÀÌÁý, ¼­¿ïÀÇ´ë ±³¼ö ÁöÁ¦±Ù, °í·ÁÀÇÇÐ ÃâÆÇ ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 1
´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
´ëÇÑÀÇÇù Çʼö ÀÇÇпë¾îÁý »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
´ëÇÑÇØºÎÇÐȸ ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
´ëÇѽŰæ¿Ü°úÇÐȸ ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
    ÇÑÀÚ
´ëÇѽŰæ¿Ü°úÇÐȸ ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
    ÇÑÀÚ
´ëÇѱâ»ýÃæÇÐȸ ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
´ëÇѱâ»ýÃæÇÐȸ ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
KI ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
KMLE ÀÇÇоà¾î »çÀü ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 1
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 1
ÀÇÇÐ³í¹® ¾àÀÚ(Pubmed/Entrez) °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 1
Çѱ¹Ç¥ÁØÁúº´»çÀκзù ¾àÀÚ ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 1
  • ÄÚµå
    ¿µ¹®
    ÇѱÛ
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