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Stock image Chromosome 15

stock image Tay-Sachs disease, a lysosomal storage genetic disorder, 3D illustration. A child with macrocephaly, and close-up view of swollen neurons with lamellar inclusions due to accumulation of gangliosides

Tay-Sachs Disease, A Lysosomal Storage Genetic Disorder, 3D Illustration. A Child With Macrocephaly, And Close-up View Of Swollen Neurons With Lamellar Inclusions Due To Accumulation Of Gangliosides

Image, 28.81MB, 11622 × 8072 jpg
stock image Tay-Sachs disease, 3D illustration. A genetic disorder that progressively destroys brain neurons, is caused by a mutation in the HEXA gene of chromosome 15 leading to deficiency of hexosaminidase A

Tay-Sachs Disease, 3D Illustration. A Genetic Disorder That Progressively Destroys Brain Neurons, Is Caused By A Mutation In The HEXA Gene Of Chromosome 15 Leading To Deficiency Of Hexosaminidase A

Image, 24.4MB, 14000 × 8436 jpg
stock image Diagnosis  Prader-Willi syndrome, pills and stethoscope.

Diagnosis Prader-Willi Syndrome, Pills And Stethoscope.

Image, 7.53MB, 5500 × 3667 jpg
stock image 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 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

Image, 2.91MB, 5000 × 4000 jpg
stock image 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 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

Image, 15.3MB, 5000 × 4000 jpg
stock image 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, Labelled 3D Illustration. A Genetic Disorder Caused By A Lack Of Function Of Part Of Chromosome 15 Inherited From A Person's Mother

Image, 2.75MB, 5000 × 4000 jpg
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