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Karyotype of normal human chromosome illustration vector
Autosome and sex chromosome, Normal human karyotype, Men and Women. DNA molecule.
Human chromosomes. Male and female karyotype, 3D 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
Karyotype of Klinefelter’s or XXY usually in male is born with an extra X chromosome (XXY).
Human karyotype illustration
Normal human male karyotype, labeled. 3D illustration
Chromosome abnormality, disorder, anomaly, aberration, or mutation
Down's syndrome karyotype, Autosomal abnormalities, Trisomy 21, vector illustration eps10
Normal human karyotype
Karyotype of normal human chromosome illustration vector
Normal human female karyotype, labeled. 3D illustration
Down syndrome karyotype
Normal human female karyotype, labeled. 3D illustration
3D Illustration showing female chromosome set, Karyotype
Philadelphia chromosome karyotype male or female. 3D illustration showing defective 9 and 22 chromosomes with translocational defect which causes cause chronic myelogenous leukaemia
Karyotyp of human male with trisomy 21 / Down Syndrome
XY-chromosomes on grey background, scientific and biology concept with depth of field effect. 3d illustration
Normal human male karyotype, labeled. 3D illustration
Down-syndrome karyotype, female, labeled, isolated on white background. Trisomy 21. 3D illustration
Double y syndrome karyotype, Nondisjunction of sex chromosomes, XYY
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
Set of human chromosomes, female karyotype, 3D illustration
Human karyotype, Autosomes and sex chromosome
Normal human karyotype
Down syndrome karyotype
Chromosomes on blue background, scientific concept 3d illustration
Genetics DNA structure  and chromosomes
Karyotype of normal human chromosome illustration vector
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
Blood sample for karyotype (abnormal chromosome study) testing
Normal human male karyotype, labeled. 3D illustration
schematic representation of human karyotype showing all chromosomes
Turners-syndrome karyotype, labeled. X0 karyotype. 3D illustration
Mutation. Chromosome abnormality: deletions, duplications, translocations, inversions, insertions and isochromosome.
Edward syndrome karyotype is the one of chromosomal disorders ( Trisomy 18)
Scheme of normal karyotype of human somatic cell 46XX and 46XY
Klinefelter syndrome karyotype
Edwards syndrome karyotype
Normal human karyotype chromosome idiogram
Human chromosome idiogram
DNA structure background and icon
Human chromosomes under a microscope
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 the microscope
Chromosomes Human under the microscope for education in Lab.
Human chromosomes under microscope view for education
Philadelphia chromosome karyotype male or female. 3D illustration showing defective 9 and 22 chromosomes with translocational defect which causes cause chronic myelogenous leukaemia
human chromosome
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
Human chromosome idiogram
Scheme of Klinefelter syndrome. karyotype of human somatic cell 47XXY
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

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Blood sample for karyotype (abnormal chromosome study) testing

Blood sample for karyotype (abnormal chromosome study) testing
Turner syndrome karyotype
Human chromosomes from blood under microscope view for education.
Chromosomes Human under the microscope for education in Lab.
Blood sample for karyotype (abnormal chromosome study) testing
Blood sample for karyotype (abnormal chromosome study) testing
Chromosomes Human under the microscope for education in Lab.
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
Patau-syndrome male karyotype, unlabeled. Trisomy 13. 3D illustration
Blood sample for karyotype testing, study for abnormal chromosome
Philadelphia chromosome karyotype male or female. 3D illustration showing defective 9 and 22 chromosomes with translocational defect which causes cause chronic myelogenous leukaemia
Genetics DNA structure  and chromosomes
DNA and Caryotype. All elements are easily accessible to selection and change
A karyotype is an individual's collection of chromosomes. The karyotype is used to look for abnormal numbers or structures of chromosomes.
Scheme of Down syndrome karyotype of human somatic cell 47XX+21 and 47XY+21
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
Patau syndrome karyotype is the one of chromosomal disorders that have extra copy of chromosome 13
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
Scheme of Jacobs (XYY) syndrome karyotype of human somatic cell 47XYY
Pregnancy planing, pregnancy management, prenatal diagnostics, assisted reproductive technology, fertilisation. Flat vector illustration for web site, landing page. Preimplantation genetic diagnosis.
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.
Down-syndrome karyotype, female, unlabeled, isolated on black background. Trisomy 21. 3D illustration

Chromosomes Human under the microscope for education in Lab.
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
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
Karyotype of Angelman syndrome, 3D illustration. A genetic disorder caused by a lack of function of part of chromosome 15 inherited from a person's mother
Karyotype of Angelman syndrome, 3D illustration. A genetic disorder caused by a lack of function of part of chromosome 15 inherited from a person's mother
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
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 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
Scheme of Robertsonian thanslocation with clinical presentation of Down syndrome karyotype of human somatic cell 46XX (or 46XY) - 14 + rob(14;21)(q10;q10)
Scheme of Turner syndrome. karyotype of human somatic cell 45X0
Down syndrome karyotype
Patau syndrome karyotype is the one of chromosomal disorders that have extra copy of chromosome 13
Genetic abstract concept. Vector color flat illustration. Set of circle frame banner of DNA helix and copy space isolated on white. Blue pink gradient Design for gene science, medicine advertisment.
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
Chromosome 18 disorders
Klinefelter's syndrome karyotype, Nondisjunction of sex chromosomes, XXY
Normal human karyotype which is the diploid pairing of the chromosomes dependant upon their number, size, and coding and controls inherited characteristics in genetics
Normal human karyotype which is the diploid pairing of the chromosomes dependant upon their number, size, and coding and controls inherited characteristics in genetics
Chromosome isolated on white background. with depth of field effect, scientific concept. 3d illustration
Turners-syndrome karyotype, labeled. X0 karyotype. 3D illustration
Down-syndrome karyotype, female, labeled, isolated on black background. Trisomy 21. 3D illustration
Turners-syndrome karyotype, unlabeled. X0 karyotype. 3D illustration
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