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Stock image Chromosome 15
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
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, 28.81MB, 11622 × 8072 jpg
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
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, 24.4MB, 14000 × 8436 jpg
Diagnosis Prader-Willi Syndrome, Pills And Stethoscope.
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, 7.53MB, 5500 × 3667 jpg
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
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, 2.91MB, 5000 × 4000 jpg
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
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, 15.3MB, 5000 × 4000 jpg
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
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, 2.75MB, 5000 × 4000 jpg
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