58 Bilder zum Thema "autosomal" bei ClipDealer

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Computer screen showing a human karyotype. Young female scientist making a karyotype in the laboratory
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
Chromosome types, colorful illustration..
Sickle Cells Blocking Blood Flow
Coronal sections of a healthy brain and a brain in Huntington's disease showing enlarged anterior horns of the lateral ventricles, degeneration and atrophy of the dorsal striatum, 3D illustration
Dorsal striatum, caudate nucleus and putamen, highlighted in the brain of a person with Huntington's disease and close-up view of neuronal degradation, conceptual 3D illustration
Human Karyotype (male and female)
Pedigree. X-linked recessive trait.
Autosomal Dominant Disorder concept
Molecule of beta-hexosaminidase A enzyme, or HEXA, 3D illustration. Mutations in the gene encoding HEXA decrease the hydrolysis of GM2 gangliosides, which is the main cause of Tay-Sachs disease
Mysterious Man in Black Hoodie. Sexy Hero Guy. Pastor or Wizard in Robe. Assassin or Witcher with Strong Face Expression in Cloak. Dark Magician Black and White Photo. Fantasy Book Cover Concept.
Midget woman singing songs with her best friend at the nature
Computer screen showing a human karyotype. Young female scientist making a karyotype in the laboratory
Neuronal inclusions in the caudate nucleus of the brain in Huntington's disease, 3D illustration. Inclusions are composed of mutated huntingtin protein, they are found in nuclei, axons and dendrites
Molecular genesis of Huntington's disease, 3D illustration. Expansion of the CAG trinucleotide sequence in the htt gene causes production of mutated Huntingtin protein leading to neurodegeneration
Scientist preparing blood samples for karyotipe and fluorescence in situ hybridization in the laminar air flow cabinet. Blood sample preparation for diagnosis. Blood test.
Book with title Joubert Syndrome on a table.
Huntington's Disease
Eye retina in Tay-Sachs disease, 3D illustration with so-called cherry-red spot. A genetic disorder that progressively destroys brain neurons, is caused by a genetic mutation in the HEXA gene
Pair of chromosomes on a blue background 3D rendering illustration. Genetics, reproduction, meiosis, science, medicine concepts.
Trisomy 18 (Edwards syndrome) - is a chromosomal condition associated with abnormalities in many parts of the body, text on notepad
Classification of chromosomes
Brain neurons in lysosomal storage diseases, Tay-Sachs, Niemann-Pick, Fabry and other. 3D illustration showing swollen neurons with lamellar inclusions due to accumulation of gangliosides in lysosomes
Pedigrees. Autosomal dominant trait and abtosomal recessive traite.
Scientific designing of Chromosome structure, illustration..
Pedigree. Autosomal recessive trait.
Sickle Cell Anemia concept
Phenylketonuria
Link between genetics and the Noonan syndrome congenital disorder
Dorsal striatum, caudate nucleus and putamen, highlighted in the brain of a person with Huntington's disease and close-up view of neuronal inclusions, conceptual 3D illustration
Intranuclear neuronal inclusions, 3D illustration. Intranuclear inclusions in neurons are found in different neurodegenerative diseases, including Huntingon's disease, spinocerebellar ataxia and other
Paper with words Sanfilippo syndrome and glasses. Medical concept.
Neuronal inclusions in Huntington's disease, 3D illustration. Inclusions are composed of mutated huntingtin protein, they are initially formed at axons and dendrites, then migrate to nuclei of neurons
Red Yellow Blue Trisomy Awareness Month ribbon in March on helping hand on grunge aged background (clipping path)
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
Paper with words Werner syndrome and glasses.
Hereditary Disorder - medical concept
Cystic fibrosis
3D rendering SCID word - severe combined immunodeficiency concept letter design isolated on white background
Autosomal recessive bestrophinopathy, ophthalmoscope view, scientific illustration showing accumulation of lipofuscin deposits around and beyond the macula leading to progressive damage to the retina
Brain neurons in lysosomal storage diseases, Tay-Sachs, Niemann-Pick, Fabry and other. 3D illustration showing swollen neurons with lamellar inclusions due to accumulation of gangliosides in lysosomes
OCA Oculocutaneous Albinism - genetic disorder characterized by skin, hair, and eye hypopigmentation due to a reduction or absence of melanin, acronym text concept background
Hypersegmented neutrophil in WHIM Syndrome - Closeup view 3d illustration
Pedigree. Autosomal dominant trait.
Best friends sitting in front of each other at the table at the summer cafe
Diagnostic form with Diagnosis Tay Sachs disease.
Link between genetics and the cystic fibrosis disorder, also known as mucoviscidosis
Intranuclear neuronal inclusions, 3D illustration. Intranuclear inclusions in neurons are found in different neurodegenerative diseases, including Huntingon's disease, spinocerebellar ataxia and other
Scientist preparing blood samples for karyotipe and fluorescence in situ hybridization in the laminar air flow cabinet. Blood sample preparation for diagnosis. Blood test.
Human chromosomes (human normal karyotype).

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