Image

Karyotype royalty-free images

519 karyotype stock photos, vectors, and illustrations are available royalty-free. See karyotype stock video clips

Popular
Karyotype of normal human chromosome illustration vector
Autosome and sex chromosome, Normal human karyotype, Men and Women. DNA molecule.
Scheme of normal karyotype of human somatic cell 46XX and 46XY
Human chromosomes. Male and female karyotype, 3D illustration
Karyotype of Klinefelter’s or XXY usually in male is born with an extra X chromosome (XXY).
Human karyotype, light micrograph. Human chromosomes stained with Giemsa (G bands).
Human karyotype illustration
Karyotype of Down syndrome (DS or DNS), also known as trisomy 21, is a genetic disorder caused by the presence of all or part of a third copy of chromosome 21
XY chromosome word on baby boy hands.kid child children gender.DNA, biotechnology, Human, XY Chromosome concept.Male Heterogametic.Fertility, ivf, sperm cell.Science for kids image background.Medical.
Karyotype of Cri du chat, or cat's cry, syndrome, 3D illustration. A rare genetic disorder caused by a partial chromosome deletion on chromosome 5. Also known as 5p- and Lejeune's syndrome
Normal human karyotype. Autosomes and sex chromosome vector.
Normal human karyotype
Normal human male karyotype, labeled. 3D illustration
Karyotype of Cri du chat, or cat's cry, syndrome, labelled 3D illustration. A rare genetic disorder caused by a partial chromosome deletion on chromosome 5. Also known as 5p- and Lejeune's syndrome
Karyotype of normal human chromosome illustration vector
Down's syndrome karyotype, Autosomal abnormalities, Trisomy 21, vector illustration eps10
Normal human female karyotype, labeled. 3D illustration
Human chromosomes under the microscope
3D Illustration showing female chromosome set, Karyotype
XY-chromosomes on grey background, scientific and biology concept with depth of field effect. 3d illustration
Normal human female karyotype, labeled. 3D illustration
Down syndrome karyotype
Philadelphia chromosome karyotype male or female. 3D illustration showing defective 9 and 22 chromosomes with translocational defect which causes cause chronic myelogenous leukaemia
Normal human male karyotype, labeled. 3D illustration
Karyotyp of human male with trisomy 21 / Down Syndrome
Double y syndrome karyotype, Nondisjunction of sex chromosomes, XYY
Sex chromosome structure. Male and Female. Biological study
Down-syndrome karyotype, female, labeled, isolated on white background. Trisomy 21. 3D illustration
schematic representation of human karyotype showing all chromosomes
Human karyotype of Down syndrome. Autosomal abnormalities. Down syndrome have an extra copy of one of these chromosomes, chromosome 21. Trisomy 21. Genetic disorder
3D illustration showing female x-choromosomes
Normal human karyotype
Chromosomes on blue background, scientific concept 3d illustration
Set of human chromosomes, female karyotype, 3D illustration
Turners-syndrome karyotype, labeled. X0 karyotype. 3D illustration
Genetics DNA structure  and chromosomes
XY-chromosomes as a concept for human biology medical symbol gene therapy or microbiology genetics research. 3d rendering
Blood sample for karyotype (abnormal chromosome study) testing
Normal human female karyotype. 3D illustration
Alteration of chromosome structure. Deletion, Duplication, Inversion, translocation.
XY Chromosome concept. Male  Heterogametic Sex.
Blood sample for karyotype (abnormal chromosome study) testing
Human karyotype of Down syndrome. Autosomal abnormalities. Trisomy 21. Genetic disorder.
Felis karyotype cat have 19 pairs  of chromosome.
Karyotype of Prader-Willi syndrome, 3D illustration. A genetic disorder caused by a lack of function of part of chromosome 15 inherited from a person's father
Human chromosomes under a microscope
Karyotype of Prader-Willi syndrome, labelled 3D illustration. A genetic disorder caused by a lack of function of part of chromosome 15 inherited from a person's father
3D ikkustration showing male chromosome set, karyotype
Scheme of Down syndrome karyotype of human somatic cell 47XX+21 and 47XY+21
Patau syndrome karyotype, Autosomal abnormalities, Trisomy 13 vector esp10
Illustration. Karyotype. Image of the chromosomes of the human being.
Human karyotype of Klinefelter syndrome. Klinefelter's, KS or XXY.
Human chromosome idiogram
Scheme of Klinefelter syndrome. karyotype of human somatic cell 47XXY
Normal human male karyotype, labeled. 3D illustration
Karyotype Test Testing Medical Concept. Checkup list medical tests with text and stethoscope
Human karyotype of Turner syndrome. One of the X chromosomes (sex chromosomes) is missing or partially missing. 45,X, or 45,X0
Genetic abstract concept. Vector color flat illustration. Set of seamless pattern of blue gradient DNA helix sign isolated on white background. Design tile for gene science web, healthcare backdrop.
Chromosome number in dog and cat. Dog and cat karyotype diagram.
Human karyotype, Autosomes and sex chromosome
Human karyotype of Turner syndrome. One of the X chromosomes (sex chromosomes) is missing or partially missing. 45,X, or 45,X0.
Mutation. Chromosome abnormality: deletions, duplications, translocations, inversions, insertions and isochromosome.
DNA structure background and icon
Human karyotype of Patau syndrome. Autosomal abnormalities. Patau syndrome have an extra copy of one of these chromosomes, chromosome 13. Trisomy 13, Genetic disorder
Human karyotype. Chromome structure. Male and Female. Biological study.
Chromosomes Human under the microscope for education in Lab.
Chromosomes Human under the microscope for education.
Human karyotype of Edwards' syndrome. Autosomal abnormalities. Edwards' syndrome have an extra copy of one of these chromosomes, chromosome 18. Trisomy 18, Genetic disorder
Human chromosome idiogram
Chromosome research for biomedical analysis of genetic abnormalities
Human karyotype of Cri du chat syndrome. Autosomal abnormalities. A piece of chromosome 5 is missing.
Chromosome number in dog. canine karyotype diagram.
Triploid syndrome karyotype. Human triploidy is a chromosomal disorder in which a fetus has three copies of every chromosome instead of the normal two. Cells have 69 chromosomes per cell
Medicine and health concept. The doctor holds in his hands a test tube with blood tests for the Karyotype, with the other hand he makes a gesture - stop.
A boy with Down syndrome cooks dough from flour and milk in the kitchen, type 21 trisonomy, a genetic anomaly, a child in a chef's costume.
Chromosome number in dog and cat. Dog and cat karyotype diagram.
3D illustration showing human chromosomes
Karyotype of Angelman syndrome, labelled 3D illustration. A genetic disorder caused by a lack of function of part of chromosome 15 inherited from a person's mother
Human karyotype. Male and Female chromosome. Biological study
human chromosome
3D illustration showing colorful female x-chromosomes
Patau syndrome karyotype is the one of chromosomal disorders that have extra copy of chromosome 13
Normal human karyotype chromosome idiogram
Human chromosomes from blood under microscope view for education.
Human karyotype of Triple x syndrome. Female has an extra X chromosome.
Chromosomes Human under the microscope for education in Lab.
Biochemist or doctor holds blood sample for karyotype test, abnormal chromosome, to identify and evaluate the size, shape, and number of chromosomes.
Structural change in the structure of chromosomes. Inversions. Paracentric inversion and pericentric inversion. Chromosomal abnormalities
Chromosomes 21, Trisomy 21, Down Syndrome
Karyotype of Turner syndrome (TS), also known 45,X, or 45,X0, is a genetic condition in which a female is partly or completely missing an X chromosome
XY-chromosomes as a concept for human biology medical symbol gene therapy or microbiology genetics research. 3d rendering
Normal human male karyotype. 3D illustration

Blood sample for karyotype (abnormal chromosome study) testing
Turner's syndrome karyotype, Nondisjunction of sex chromosomes, Monosomy X
Human karyotype of Klinefelter syndrome. Klinefelter's, KS or XXY.
Human karyotype of Triple x syndrome. Female has an extra X chromosome.
Human karyotype of Patau syndrome. Autosomal abnormalities. Trisomy 13. Genetic disorder.
Human karyotype of Edwards' syndrome. Autosomal abnormalities. Trisomy 18. Genetic disorder.
Human karyotype of Double y syndrome. XYY. Male has an extra Y chromosome.
Structural change in the structure of chromosomes. Deletion. Chromosomal abnormalities
of 1