Category:Chromosomal abnormalities

Subcategories

This category has the following 21 subcategories, out of 21 total.

Media in category "Chromosomal abnormalities"

The following 160 files are in this category, out of 160 total.

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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, 11 pages; 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, 7 pages; 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, 10 pages; 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, 4 pages; 2.68 MB
  
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  Малая сверхчисленная маркерная хромосома.pdf 1,239 × 1,752, 5 pages; 3.29 MB
  
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  Молекулярноцитогенетическое исследование детей, родившихся недоношенными.pdf 1,239 × 1,752, 27 pages; 1.97 MB
  
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  Спектр редких хромосомных аномалий, выявленных пренатально у плодов.pdf 1,239 × 1,712, 5 pages; 406 KB
  
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  Цитогенетика репродуктивных нарушений у мужчин.pdf 1,179 × 1,687, 6 pages; 456 KB
  
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  Частичная моносомия 6q.pdf 1,239 × 1,712, 4 pages; 541 KB
  
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  Частичная трисомия 2q.pdf 1,179 × 1,687, 4 pages; 140 KB
  
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  איחוי של כרומוזום 2.png 291 × 192; 4 KB