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"chromosome banding"¿¡ ´ëÇÑ °Ë»ö °á°úÀÔ´Ï´Ù. °Ë»ö °á°ú º¸´Â µµÁß¿¡ Tab ۸¦ ´©¸£½Ã¸é °Ë»ö âÀÌ ¼±Åõ˴ϴÙ.
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  • ¿µ¹®
    ÇѱÛ
  • chromosome grouping
    ¿°»öüºÐ·ù(¹ý), ¿°»öü±ºº°(¹ý)
  • chromosome imbalance
    ¿°»öüºÒ±ÕÇü
  • chromosome map
    ¿°»öüÁöµµ
  • chromosome mapping
    ¿°»öüÁöµµÈ­
  • chromosome mutation
    ¿°»öüµ¹¿¬º¯ÀÌ
  • chromosome recombination
    ¿°»öüÀçÁ¶ÇÕ
  • chromosome segregation
    ¿°»öüºÐ¸®
  • chromosome walking
    ¿°»öüÀ̵¿
  • daughter chromosome
    µþ¿°»öü
  • dicentric chromosome
    µÎ¸Åµì¿°»öü, ½Öµ¿¿øÃ¼¿°»öü
  • diploid chromosome
    µÎ¹è¼öü¿°»öü
  • homologous chromosome
    »óµ¿¿°»öü
  • inversion of chromosome
    ¿°»öüÀÚ¸®¹Ù²Þ
  • lampbrush chromosome
    ·¥ÇÁºê·¯½¬¿°»öü
  • mitochondrial chromosome
    »ç¸³Ã¼¿°»öü, ¹ÌÅäÄܵ帮¾Æ¿°»öü
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
  • chromosome imbalance
    ¿°»öüºÒ±ÕÇü
  • chromosome map
    ¿°»öüÁöµµ
  • chromosome matrix
    ¿°»öü¹ÙÅÁÁú
  • chromosome recombination
    ¿°»öüÀçÁ¶ÇÕ
  • chromosome translocation
    ¿°»öüÀüÀ§
  • chromosome walking
    ¿°»öüÀ̵¿
  • circular chromosome
    °í¸®¿°»öü
  • daughter chromosome
    µþ¿°»öü
  • dicentric chromosome
    ½ÖÁß½ÉÀý¿°»öü
  • diploid chromosome
    µÎ¹è¼ö¿°»öü
  • homologous chromosome
    »óµ¿¿°»öü
  • lampbrush chromosome
    ·¥ÇÁºê·¯½¬¿°»öü
  • manad chromosome
    ÀϺп°»öü
  • meiotic chromosome
    ¿°»öü³ª¼±, °¨¼öºÐ¿­¿°»öü
  • metacentric chromosome
    Á߾Ӹŵ쿰»öü
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 6 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
  • homologous chromosome
    »óµ¿¿°»öü
  • ph chromosome
    Ph¿°»öü(¡­æøßäô÷), Çʶóµ¨ÇǾƿ°»öü(¡­æøßäô÷)
  • philadephia chromosome
    Çʶóµ¨ÇǾƿ°»öü(¡­æøßäô÷)
  • polycentric chromosome
    ¹µÁß½ÉÀý¿°»öü
  • quadrivalent chromosome
    ³×¹è¼ö¿°»öü
  • reduction of chromosome
    ¿°»öü°¨¼ö(æøßäô÷Êõâ¦).
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
  • chromosome
    ¿°»öü
  • chromosome
    ¿°»öü(æøßäô÷)
  • chromosome
    ¿°»öü
  • chromosome 21
    ¿°»öü21
  • chromosome aberration
    ¿°»öüÀÌ»ó
  • chromosome abnormality
    ¿°»öü ÀÌ»ó(¡­ì¶ßÈ).
  • chromosome association
    ¿°»öüÁ¢ÇÕ(¡­ïÈùê).
  • chromosome breakage
    ¿°»öü¼Õ»ó
  • chromosome bridge
    ¿°»öü±³(¡­Îé).
  • chromosome chain
    ¿°»öü¼â(¡­áð).
  • chromosome configuration
    ¿°»öüÁ¢ÇÕÇü(¡­ïÈùêû¡).
  • chromosome imbalace
    ¿°»öüºÒ±ÕÇü
  • chromosome longarm deletion syndrome
    ¿°»öüÀåÁö°á¼ÕÁõÈıº(¡­íþò¦ÌÀáßñøý¦ÏØ).
  • chromosome map
    ¿°»öüÁöµµ (æøßäô÷ò¢Óñ).
  • chromosome matrix
    ¿°»öü±âÁú(¡­Ñ¨òõ).
´ëÇÑÇØºÎÇÐȸ ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 13 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
  • Meiotic chromosome
    °¨¼öºÐ¿­¿°»öü
    [¿¾ ¿ë¾î] °¨¼öºÐ¿­¿°»öü
  • Telocentric chromosome
    ³¡Áß½ÉÀý¿°»öü
    [¿¾ ¿ë¾î] Á¾µ¿¿øÃ¼¿°»öü
  • Polycentric chromosome
    ¹µÁß½ÉÀý¿°»öü
    [¿¾ ¿ë¾î] ´Ùµ¿¿øÃ¼¿°»öü
  • Dicentric chromosome
    ½ÖÁß½ÉÀý¿°»öü
    [¿¾ ¿ë¾î] ½Öµ¿¿øÃ¼¿°»öü
  • Monocentric chromosome
    ȬÁß½ÉÀý¿°»öü
    [¿¾ ¿ë¾î] ´Üµ¿¿øÃ¼¿°»öü
  • Y-chromosome
    ³²¼º¿°»öü [Y¿°»öü]
    [¿¾ ¿ë¾î] Y¿°»öü
  • Y-chromosome
    ³²¼º¿°»öü [Y¿°»öü]
    [¿¾ ¿ë¾î] Y-¿°»öü
  • Homologous chromosome
    »óµ¿¿°»öü
    [¿¾ ¿ë¾î] »óµ¿¿°»öü
  • Sex chromosome
    ¼º¿°»öü
    [¿¾ ¿ë¾î] ¼º¿°»öü
  • Mother chromosome
    ¾î¹Ì¿°»öü
    [¿¾ ¿ë¾î] ¸ð¿°»öü
  • X-chromosome
    ¿©¼º¿°»öü [X¿°»öü]
    [¿¾ ¿ë¾î] X¿°»öü
  • X-chromosome
    ¿©¼º¿°»öü [X¿°»öü]
    [¿¾ ¿ë¾î] X-¿°»öü
  • Chromosome
    ¿°»öü
    [¿¾ ¿ë¾î] ¿°»öü
´ëÇÑ»ýÈ­ÇкÐÀÚ»ý¹°ÇÐȸ ¿ë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
  • limited chromosome
    Á¦ÇÑ¿°»öü(ð¤ùÚæøßäô÷)
  • polytene chromosome
    ´Ù»ç ¿°»öü(ÒýÞêæøßäô÷)
  • sex chromosome
    ¼º¿°»öü(àõæøßäô÷)
  • X chromosome
    X ¿°»öü (æøßäô÷)
  • Y chromosome
    Y ¿°»öü (æøßäô÷)
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 2
CHC chromosome condensation; community health center; community health computing; community health counc...
chr chromosome; chronic
CMGT chromosome-mediated gene transfer
CMS children's medical services; Christian Medical Society; chronic myelodysplastic syndrome; chromosome...
cs chromosome; consciousness
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 2
CHr Chromosome
CA Chromosome aberration
CMGT Chromosome mediated gene transfer
CCR Complex chromosome rearrangements
FTDP-17 Frontotemporal dementia and Parkinsonism linked to chromosome 17
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • chromosome recombination
    ¿°»öü Àç°áÇÕ
  • chromosome-breakage syndrome
    ¿°»öü-ºÐÇØ ÁõÈıº
  • circular chromosome
    ȯ»ó ¿°»öü
  • extra chromosome
    °úÀ× ¿°»öü
    »ý¹° Á¾¿¡ À־ Á¤»óÀûÀÎ ¿°»öü ±¸¼º¿øÀÌ ¾Æ´Ñ ¿°»öü. Áï, »ý¹°Àº Á¾¸¶´Ù ÀÏÁ¤ÇÑ ¿°»öü ¼ö·Î ÇÑ Á¶¸¦ ÀÌ·é´Ù. ÀÌ ¿°»öü Á¶ÀÇ Á¤»óÀûÀÎ ±¸¼º¿ø
  • homologous chromosome
    »óµ¿ ¿°»öü
    ÇüÅÂ¿Í ÇÔÀ¯Çϰí ÀÖ´Â À¯ÀüÀÚ°¡ ½ÖÀÌ µÉ ¼ö ÀÖ´Â 1½ÖÀÇ ¿°»öü. º¸Åë »ý¹°Àº 2¹è¼ºÀ̸ç 2Á¶ÀÇ ¿°»öü¸¦ °¡Áö°í ÀÖÀ¸¹Ç·Î °¢ ¿°»öü´Â ½ÖÀÌ µÉ ¼ö ÀÖ´Ù. »óµ¿ ¿°»öü´Â ÇÙ ºÐ¿­À» ÇÒ ¶§ ¹Ýµå½Ã ÀÎÁ¢ÇÏ¿© Á¸ÀçÇÏ´Â °ÍÀº ¾Æ´ÏÁö¸¸, °¨¼öºÐ¿­ÀÇ Á߱⿡´Â Á¢ÇÕÇÏ¿© »óÁ¢Çϸç, Èı⿡´Â ºÐ¸®ÇÏ¿© ¹Ý´ëÀÇ ±ØÀ¸·Î ³ª´©¾îÁø´Ù. ¶§·Î´Â »óµ¿ ¿°»öü°¡ ºÎµîÇüÀ» ÀÌ·ç´Â °æ¿ì°¡ Àִµ¥, X ¿°»öü³ª Y ¿°»öü µîÀÌ ÀÌ¿¡ ¼ÓÇÑ´Ù.
  • lampbrush chromosome
    ·¥ÇÁ ºê·¯½Ã ¿°»öü
    ôÃß, ¹«Ã´Ãßµ¿¹°ÀÇ °¨¼öºÐ¿­ Àü±âÀÇ µðÇ÷ÎÅٱ⿡¼­ ³­¸ð¼¼Æ÷ ÇÙÀÇ °Å´ëÇÑ 2°¡ ¿°»öü ¹× ³ë¶û ÃÊÆÄ¸®·ùÀÇ Á¤¸ð¼¼Æ÷ ÇÙ ³»ÀÇ Y ¿°»öü¿¡¼­ °üÂûµÇ´Â ¿°»öü. ÁÖÃà¿¡ µû¶ó ¸¹Àº ¼öÀÇ ·çÇÁ ¸ð¾çÀÇ µ¹Ãâ¹°ÀÌ ¿·¿¡¼­ ³ª¿Í ÀÖ¾î ¿°»öü Àüü°¡ ¾óÇÍ º¸¾Æ ·¥ÇÁ¸¦ ´Û´Â ºê·¯½Ã¿Í °°ÀÌ »ý°å´Ù°í ÇØ¼­ ÀÌ·± À̸§ÀÌ ºÙ¿©Á³´Ù. ¿°»öºÐüÀÇ »óµ¿ ºÎºÐÀÌ ¼­·Î ¸Â´ë°í ÀÖ°í, DNA¿Í ´Ü¹éÁú·Î ±¸¼ºµÇ´Â ºñÈÄÇÑ ÀÔÀÚ ¸ð¾çÀÇ ÁÖÃà ºÎºÐ°ú, °Å±â¿¡¼­ ÇÑ ½Ö¾¿ ¿·À¸·Î ³­ DNA ¼¶À¯¿Í ¸®º¸ ÇÙ ´Ü¹éÁú·Î ÀÌ·ç¾îÁø ·çÇÁ ±¸Á¶ ºÎºÐÀ¸·Î µÇ¾î ÀÖ´Ù. ¿µ¿ø
  • mapping chromosome
    ÁöµµÈ­ ¿°»öü
    ¼­·Î ¿¬¼âµÇ¾î ÀÖ´Â À¯ÀüÀÚÀÇ °¢°¢ÀÇ À§Ä¡¸¦ ¿°»öü À§ÀÇ »ó´ëÀûÀÎ ¼ø¼­³ª °Å¸®¿¡ µû¶ó¼­ ÇÑ °¡´ÚÀÇ Á÷¼± À§¿¡ µµ½ÄÀûÀ¸·Î ±×·ÁÁø ¿°»öü.
  • matrix of chromosome
    ¿°»öü ¹ÙÅÁÁú
  • meiotic chromosome
    °¨¼ö ºÐ¿­ ¿°»öü, ¿°»öü ³ª¼±
  • metacentric chromosome
    Áß¾Ó µ¿¿øÃ¼, Áß¾Ó Áß½ÉÀý ¿°»öü
  • monocentric chromosome
    Ȭ Áß½ÉÀý ¿°»öü
  • morphological aberration of chromosome
    ¿°»öü ÇüÅ ÀÌ»ó
  • quadrivalent chromosome
    ³×¹è¼ö ¿°»öü
  • rearrangement chromosome
    Àç¹è¿­ ¿°»öü
  • ring chromosome
    °í¸® ¿°»öü
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
high-resolution banding Banding, especially in prophase, which increases the clarity and number of discernible chromosome bands.
(05 Mar 2000)
pulmonary artery banding A surgical method of decreasing pulmonary blood flow and thereby volume overload of the left ventricle, alleviating CHF in certain congenital heart defects.
(05 Mar 2000)
NOR-banding A procedure which utilises a silver stain that preferentially accumulates in the nucleoli-organizing regions, i.e., the satellite regions of the acrocentric chromosomes.
(05 Mar 2000)
Q-banding <cell biology, technique> A fluorescent stain for chromosomes which produces specific banding patterns for each pair of homologous chromosomes.
The acridine dye derivative, quinacrine hydrochloride, or other derivatives like quinacrine mustard dihydrochloride produces a green-yellow fluorescence at pH 4.5 in chromosome segments rich in constitutive heterochromatin with deoxyadenylate-deoxythymidilate (A-T) bases of DNA.
The centromeric regions of human chromosomes 3, 4, and 13 are specifically stained, as are satellites of some acrocentric chromosomes and the end of the long arm of the Y chromosome.
Banding patterns are similar to those obtained with G-banding stain and similar fluorescent stain results are seen with the antibiotics adriamycin and daunomycin, as well as the tertiary dyes butyl proflavine and dapi, and the bisbenzimidazole dye hoechst 33258.
See: banding patterns, Q bands, quinacrine.
Synonym: quinacrine chromosome banding stain.
(12 Jul 2000)
telomeric R-banding stain <technique> A modified R-banding stain in which the telomeres become strongly stained and faint R-banding still occurs over the rest of the chromosomes; uses air-dried slides, aging for several days, and staining in hot phosphate-buffered Giemsa stain.
(05 Mar 2000)
Trusler's rule for pulmonary artery banding A method that gives guidance as to the correct tightness of the band; the degree of banding for a complex congenital cardiac anomaly with bidirectional shunting less than that for simple ones.
(05 Mar 2000)
trypsin G-banding stain <technique> A unique chromosome staining technique, used in human cytogenetics to identify individual chromosomes, which produces characteristic bands.
It utilises acetic acid fixation, air drying, denaturing chromosomes mildly with proteolytic enzymes, salts, heat, detergents, or urea, and finally Giemsa stain; chromosome bands appear similar to those fluorochromed by Q-banding stain.
Synonym: Giemsa chromosome banding stain.
(05 Mar 2000)
accessory chromosome A chromosome existing without its normal homologous chromosome; at the reduction division of gametogenesis an accessory chromosome is likely to be included in one daughter cell and not in the other, but may be lost completely by lagging behind on the equatorial plate.
Synonym: monosome, odd chromosome, unpaired allosome, unpaired chromosome.
(05 Mar 2000)
acentric chromosome A fragment of a chromosome lacking a centromere and unable to attach to the mitotic spindle, therefore unable to take part in the division of a nucleus and randomly distributed in daughter cells.
Synonym: acentric fragment.
(05 Mar 2000)
acrocentric chromosome A chromosome with the centromere placed very close to one end so that the short arm is very small, often with a satellite.
(05 Mar 2000)
balanced chromosome <genetics> A chromosome which is unable to pair with its homologue and participate in homologus recombination during meiosis because it contains several inversion mutations (that is, has segments which have become flip-flopped).
(09 Oct 1997)
B chromosome <genetics> Small acentric chromosome, part of the normal genome of some races and species of plants.
(18 Nov 1997)
bivalent chromosome A pair of chromosome's temporarily united.
(05 Mar 2000)
male chromosome complement The large majority of males have a 46, xy chromosome complement (46 chromosomes including an x and a y chromosome). A minority of males have other chromosome constitutions such as 47,xxy (47 chromosomes including two x chromosomes and a y chromosome) and 47,xyy (47 chromosomes including an x and two y chromosomes).
(12 Dec 1998)
marker chromosome An abnormal chromosome that is distinctive in appearance but not fully identified. For example, the fragile x chromosome was once called the marker x.
(12 Dec 1998)
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