Category:Chromosomal abnormalities

하위 분류

다음은 이 분류에 속하는 하위 분류 21개 가운데 21개입니다.

"Chromosomal abnormalities" 분류에 속하는 미디어

다음은 이 분류에 속하는 파일 160개 가운데 160개입니다.

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  1536px Քրոմոսոմներ և նրանց հետ կապակցված հիվանդություններ.png 1,536 × 1,275; 349 KB
  
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  16p11.2 deletion.jpg 416 × 455; 23 KB
  
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  17p11.jpg 140 × 290; 47 KB
  
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  1p36 del.png 800 × 1,424; 191 KB
  
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  21 chr x 3.JPG 1,017 × 896; 24 KB
  
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  2q23.1 del.png 370 × 1,334; 134 KB
  
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  3q27.3 microdeletion.png 782 × 1,221; 273 KB
  
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  7q11.23 duplication.png 589 × 2,053; 322 KB
  
• A-Universal-Mechanism-Ties-Genotype-to-Phenotype-in-Trinucleotide-Diseases-pcbi.0030235.sv001.ogv 30 s, 560 × 420; 407 KB
  
• A-Universal-Mechanism-Ties-Genotype-to-Phenotype-in-Trinucleotide-Diseases-pcbi.0030235.sv002.ogv 38 s, 560 × 420; 401 KB
  
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  Abortion Karyotype.pdf 1,239 × 1,712, 11쪽; 1.2 MB
  
• Centromere-Independent-Accumulation-of-Cohesin-at-Ectopic-Heterochromatin-Sites-Induces-Chromosome-pbio.1001962.s013.ogv 12 s, 614 × 320; 465 KB
  
• Centromere-Independent-Accumulation-of-Cohesin-at-Ectopic-Heterochromatin-Sites-Induces-Chromosome-pbio.1001962.s014.ogv 5.3 s, 500 × 250; 191 KB
  
• Centromere-Independent-Accumulation-of-Cohesin-at-Ectopic-Heterochromatin-Sites-Induces-Chromosome-pbio.1001962.s015.ogv 3.7 s, 240 × 240; 63 KB
  
• Centromere-Independent-Accumulation-of-Cohesin-at-Ectopic-Heterochromatin-Sites-Induces-Chromosome-pbio.1001962.s016.ogv 5.3 s, 299 × 241; 138 KB
  
• Centromere-Independent-Accumulation-of-Cohesin-at-Ectopic-Heterochromatin-Sites-Induces-Chromosome-pbio.1001962.s017.ogv 5.8 s, 268 × 160; 90 KB
  
• Centromere-Independent-Accumulation-of-Cohesin-at-Ectopic-Heterochromatin-Sites-Induces-Chromosome-pbio.1001962.s018.ogv 13 s, 236 × 354; 141 KB
  
• Centromere-Independent-Accumulation-of-Cohesin-at-Ectopic-Heterochromatin-Sites-Induces-Chromosome-pbio.1001962.s019.ogv 9.3 s, 346 × 384; 477 KB
  
• Centromere-Independent-Accumulation-of-Cohesin-at-Ectopic-Heterochromatin-Sites-Induces-Chromosome-pbio.1001962.s020.ogv 14 s, 298 × 190; 283 KB
  
• Centromere-Independent-Accumulation-of-Cohesin-at-Ectopic-Heterochromatin-Sites-Induces-Chromosome-pbio.1001962.s021.ogv 3.7 s, 280 × 140; 44 KB
  
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  CFTR gene on chromosome 7.svg 75 × 487; 6 KB
  
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  Chromosome 18 (Partial Deletion of the Long Arm) 1.jpg 926 × 1,157; 413 KB
  
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  Chromosome 18 (Partial Deletion of the Long Arm) 2.jpg 936 × 1,173; 367 KB
  
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  Chromosome 2 merge en.svg 270 × 180; 12 KB
  
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  Chromosome 2 merge es.svg 270 × 180; 12 KB
  
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  Chromosome arabic mutations.pdf 1,239 × 1,754; 25 KB
  
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  Chromosome disorder.png 2,048 × 1,536; 4.78 MB
  
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  Chromosome duplication.jpg 370 × 400; 37 KB
  
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  Chromosome français b.pdf 1,239 × 1,754; 22 KB
  
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  Chromosome français.pdf 1,239 × 1,754; 22 KB
  
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  Chromosome mutation.png 326 × 1,062; 30 KB
  
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  Chromosome mutations-ar.svg 592 × 1,206; 317 KB
  
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  Chromosome2 merge af.svg 270 × 180; 8 KB
  
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  Chromosome2 merge ar.svg 270 × 180; 29 KB
  
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  Chromosome2 merge nl.svg 270 × 180; 6 KB
  
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  Chromosome2 merge.png 291 × 192; 3 KB
  
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  Chromosomenmutation.png 311 × 416; 20 KB
  
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  Chromosomenmutationen Dutch text.png 868 × 974; 140 KB
  
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  Chromosomenmutationen.png 434 × 487; 23 KB
  
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  Chromosomes mutations ku.svg 606 × 1,198; 183 KB
  
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  Chromosomes mutations-cs.svg 606 × 1,198; 180 KB
  
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  Chromosomes mutations-en.svg 606 × 1,198; 180 KB
  
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  Chromosomes mutations-es.svg 606 × 1,198; 182 KB
  
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  Chromosomes mutations-mk.svg 606 × 1,198; 300 KB
  
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  Chromosomes mutations-pl.svg 606 × 1,198; 180 KB
  
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  Chromosone arabic b.pdf 1,239 × 1,754; 25 KB
  
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  Chromothripsis the result of a single catastrophic event in a cells history.png 599 × 419; 8 KB
  
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  Chromothripsis.svg 380 × 221; 142 KB
  
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  DECIPHER example.png 1,600 × 506; 32 KB
  
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  Delecion.png 469 × 496; 170 KB
  
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  Deletion of chromosome section -kn.svg 238 × 371; 23 KB
  
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  Deletion of chromosome section as.svg 238 × 371; 19 KB
  
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  Deletion of chromosome section fr.svg 238 × 371; 19 KB
  
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  Deletion of chromosome section ml.svg 238 × 371; 26 KB
  
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  Deletion of chromosome section-bn.svg 238 × 371; 28 KB
  
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  Deletion of chromosome section-es.svg 238 × 371; 19 KB
  
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  Deletion of chromosome section-gu.svg 238 × 371; 19 KB
  
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  Deletion of chromosome section-hi.png 238 × 371; 11 KB
  
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  Deletion of chromosome section-hi.svg 238 × 371; 23 KB
  
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  Deletion of chromosome section-mr.svg 238 × 371; 28 KB
  
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  Deletion of chromosome section-pa.svg 238 × 371; 25 KB
  
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  Deletion of chromosome section-ta.svg 238 × 371; 26 KB
  
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  Deletion of chromosome section-te.svg 238 × 371; 24 KB
  
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  Deletion of chromosome section.png 238 × 371; 7 KB
  
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  Deletion of chromosome section.svg 238 × 371; 19 KB
  
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  Diagram of genetic mutations to the chromosone in arabic.pdf 1,239 × 1,754; 25 KB
  
• Direct-Unequal-Cleavages-Embryo-Developmental-Competence-Genetic-Constitution-and-Clinical-Outcome-pone.0166398.s008.ogv 22 s, 500 × 500; 7.3 MB
  
• Direct-Unequal-Cleavages-Embryo-Developmental-Competence-Genetic-Constitution-and-Clinical-Outcome-pone.0166398.s009.ogv 27 s, 500 × 500; 7.5 MB
  
• Direct-Unequal-Cleavages-Embryo-Developmental-Competence-Genetic-Constitution-and-Clinical-Outcome-pone.0166398.s010.ogv 27 s, 500 × 500; 9.42 MB
  
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  Doublement chromatique.png 293 × 692; 23 KB
  
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  Down syndrome translocation.png 1,077 × 1,159; 177 KB
  
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  Duplicació gènica.png 508 × 777; 26 KB
  
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  Duplication interne.png 518 × 474; 12 KB
  
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  Déplacement 13 10.png 431 × 575; 28 KB
  
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  Déplacement chromo.png 387 × 607; 25 KB
  
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  Effacement chromosome.png 273 × 580; 21 KB
  
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  Enchâssement complexe.png 289 × 449; 20 KB
  
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  Enchâssement simple 2.png 293 × 530; 22 KB
  
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  Enchâssement simple.png 216 × 387; 17 KB
  
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  Enjambement inégal.png 407 × 488; 28 KB
  
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  Gene-duplication cropped.png 143 × 353; 7 KB
  
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  Gene-duplication esp.png 508 × 777; 15 KB
  
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  Gene-duplication vi.png 508 × 777; 19 KB
  
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  Gene-duplication-notext.png 136 × 352; 10 KB
  
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  Gene-duplication-zh-hant.png 508 × 777; 18 KB
  
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  Gene-duplication.png 508 × 777; 20 KB
  
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  Gene-duplication.svg 130 × 354; 13 KB
  
• Genetic-dosage-and-position-effect-of-small-supernumerary-marker-chromosome-(sSMC)-in-human-sperm-srep17408-s2.ogv 8.4 s, 240 × 240; 695 KB
  
• Genetic-dosage-and-position-effect-of-small-supernumerary-marker-chromosome-(sSMC)-in-human-sperm-srep17408-s3.ogv 33 s, 320 × 240; 245 KB
  
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  Human chromosome diseases set en.png 2,000 × 1,660; 553 KB
  
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  Human chromosome diseases set en.svg 512 × 425; 3.56 MB
  
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  Human triploid karyotype.jpg 618 × 240; 46 KB
  
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  Insertion chromosomique.gif 473 × 334; 19 KB
  
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  Insertion-genetics-es.png 1,000 × 691; 36 KB
  
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  Insertion-genetics.png 1,004 × 693; 16 KB
  
• Intratumour-Diversity-of-Chromosome-Copy-Numbers-in-Neuroblastoma-Mediated-by-On-Going-Chromosome-pone.0059268.s005.ogv 14 s, 265 × 169; 1.05 MB
  
• Intratumour-Diversity-of-Chromosome-Copy-Numbers-in-Neuroblastoma-Mediated-by-On-Going-Chromosome-pone.0059268.s006.ogv 1 min 40 s, 642 × 644; 5.03 MB
  
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  Inverzija.jpg 400 × 285; 23 KB
  
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  Isochromosome1 miguelferig.png 1,162 × 792; 31 KB
  
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  Izohromozomi.jpg 729 × 454; 47 KB
  
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  Kromosoommutatsioonid.png 500 × 540; 20 KB
  
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  Micronuclei and nuclear abnormalities in peripheral blood erythrocytes of penguins Pygoscelis papua 1.JPG 654 × 669; 52 KB
  
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  Mosaicism for combined tetrasomy of chromosomes 8 and 18 in a dysmorphic child - A result of failed tetraploidy correction?.pdf 1,270 × 1,650, 7쪽; 1.71 MB
  
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  Mucoviscidose.PNG 86 × 498; 3 KB
  
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  Mutaatiotyypit.png 259 × 586; 38 KB
  
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  Mutation deletion.jpg 75 × 142; 3 KB
  
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  Mutation insertion.jpg 199 × 141; 5 KB
  
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  Mutation translocation.jpg 205 × 144; 29 KB
  
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  MutációTípusok.svg 495 × 448; 99 KB
  
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  Non allelic homologous recombination.png 665 × 585; 46 KB
  
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  Non-allelic Homologous Recombination.svg 512 × 366; 238 KB
  
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  Nuclear abnormalities in peripheral blood erythrocytes of penguins Pygoscelis papua 3.JPG 664 × 624; 40 KB
  
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  Nuclear abnormalities in peripheral blood erythrocytes of penguins Pygoscelis papua 4.JPG 664 × 636; 36 KB
  
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  Numerical chromosome aberration.png 2,048 × 1,536; 4.69 MB
  
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  OGrady1897-2.jpg 591 × 849; 178 KB
  
• Over-Expression-of-DSCAM-and-COL6A2-Cooperatively-Generates-Congenital-Heart-Defects-pgen.1002344.s011.ogv 4.6 s, 1,128 × 808; 3.27 MB
  
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  Pericentricna inverzija.jpg 400 × 200; 19 KB
  
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  Philadelphia chromosome detection.jpg 563 × 669; 133 KB
  
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  PSM V27 D034 The hoagland family of kentucky genealogy.jpg 2,361 × 1,008; 112 KB
  
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  PSM V27 D035 The fullerton family of hebron new york genealogy.jpg 1,346 × 992; 56 KB
  
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  PSM V88 D111 Forty two year old mentally disabled man.png 356 × 807; 70 KB
  
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  PSM V88 D111 Microcephalic boy.png 511 × 813; 62 KB
  
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  PSM V88 D111 Twin egg monster before development.png 981 × 567; 116 KB
  
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  PSM V88 D112 Physically disfigured children with mental disabilities.png 2,019 × 1,371; 947 KB
  
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  PSM V88 D113 Animals with birth defects.png 2,036 × 2,392; 808 KB
  
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  PSM V88 D114 Birth defects in fish and frogs.png 1,040 × 1,018; 151 KB
  
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  PSM V88 D114 Twin dog fish due to chemical effect on the egg.png 965 × 1,299; 303 KB
  
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  Relation 1q21 1.jpg 438 × 152; 11 KB
  
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  Ring Chromosome 18 1.jpg 927 × 1,366; 521 KB
  
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  Ring Chromosome 18 2.jpg 928 × 1,373; 472 KB
  
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  Schematic illustration of chromosomal aberrations.svg 404 × 246; 200 KB
  
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  Signatures of SVs in various detection methods.jpg 1,180 × 829; 297 KB
  
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  Single Chromosome Mutations.png 752 × 544; 15 KB
  
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  Single Chromosome Mutations.svg 752 × 544; 12 KB
  
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  SRY-Translocation de.svg 837 × 839; 14 KB
  
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  Tetravalent.jpg 694 × 631; 79 KB
  
• The-Cellular-Phenotype-of-Roberts-Syndrome-Fibroblasts-as-Revealed-by-Ectopic-Expression-of-ESCO2-pone.0006936.s001.ogv 12 s, 1,392 × 1,040; 4.42 MB
  
• The-Cellular-Phenotype-of-Roberts-Syndrome-Fibroblasts-as-Revealed-by-Ectopic-Expression-of-ESCO2-pone.0006936.s002.ogv 21 s, 720 × 480; 660 KB
  
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  Three chromosomal abnormalities with ISCN nomenclature.png 916 × 519; 190 KB
  
• Timeless-Links-Replication-Termination-to-Mitotic-Kinase-Activation-pone.0019596.s009.ogv 26 s, 760 × 682; 1.42 MB
  
• Timeless-Links-Replication-Termination-to-Mitotic-Kinase-Activation-pone.0019596.s010.ogv 26 s, 762 × 684; 954 KB
  
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  Total premature chromatide division with centric ring.jpg 718 × 570; 85 KB
  
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  Translocación.png 697 × 617; 304 KB
  
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  Translokacija 14-21.jpg 353 × 623; 38 KB
  
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  Translokacija 21-21.jpg 400 × 600; 32 KB
  
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  Types-of-mutation.png 259 × 586; 37 KB
  
• Uncovering-Genomic-Causes-of-Co-Morbidity-in-Epilepsy-Gene-Driven-Phenotypic-Characterization-of-pone.0023182.s006.ogv 2.0 s, 432 × 252; 111 KB
  
• Uncovering-Genomic-Causes-of-Co-Morbidity-in-Epilepsy-Gene-Driven-Phenotypic-Characterization-of-pone.0023182.s007.ogv 1.9 s, 432 × 252; 115 KB
  
• Uncovering-Genomic-Causes-of-Co-Morbidity-in-Epilepsy-Gene-Driven-Phenotypic-Characterization-of-pone.0023182.s008.ogv 2.0 s, 432 × 252; 149 KB
  
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  YChromosom Evolution.jpg 589 × 334; 84 KB
  
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  Биомаркеры неонкологических болезней мозга, обусловленных хромосомной нестабильностью, у детей.pdf 1,239 × 1,752, 10쪽; 2.02 MB
  
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  Диплохромосоми.jpg 1,606 × 2,002; 662 KB
  
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  Замерзшая беременность.pdf 1,297 × 1,770, 4쪽; 2.68 MB
  
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  Малая сверхчисленная маркерная хромосома.pdf 1,239 × 1,752, 5쪽; 3.29 MB
  
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  Молекулярноцитогенетическое исследование детей, родившихся недоношенными.pdf 1,239 × 1,752, 27쪽; 1.97 MB
  
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  Спектр редких хромосомных аномалий, выявленных пренатально у плодов.pdf 1,239 × 1,712, 5쪽; 406 KB
  
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  Цитогенетика репродуктивных нарушений у мужчин.pdf 1,179 × 1,687, 6쪽; 456 KB
  
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  Частичная моносомия 6q.pdf 1,239 × 1,712, 4쪽; 541 KB
  
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  Частичная трисомия 2q.pdf 1,179 × 1,687, 4쪽; 140 KB
  
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  איחוי של כרומוזום 2.png 291 × 192; 4 KB