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Search results for: inherited

Pelger-Huet anomaly, LM
SS21336524
RM
Nature's Faces / Science Source
Pelger-Huet anomaly, LM
Elliptocytosis, LM
SS21337165
RM
Nature's Faces / Science Source
Elliptocytosis, LM
Pelger-Huet anomaly, LM
SS21336776
RM
Nature's Faces / Science Source
Pelger-Huet anomaly, LM
Pelger-Huet anomaly, LM
SS21336630
RM
Nature's Faces / Science Source
Pelger-Huet anomaly, LM
Pelger-Huet anomaly, LM
SS21336554
RM
Nature's Faces / Science Source
Pelger-Huet anomaly, LM
Pelger-Huet anomaly, LM
SS21336523
RM
Nature's Faces / Science Source
Pelger-Huet anomaly, LM
Hereditary pyropoikilocytosis, LM
SS21335827
RM
Nature's Faces / Science Source
Hereditary pyropoikilocytosis, LM
Hereditary elliptocytosis, LM
SS21335825
RM
Nature's Faces / Science Source
Hereditary elliptocytosis, LM
Down Syndrome Human Karyotype
SS2871921
RM
Wellcome Images / Science Source
Down Syndrome Human Karyotype
Occular Albinism
SS2777612
RM
Clinical Photography, Central Manchester University Hospitals NHS Foundation Trust, UK / Science Source
Occular Albinism
Occular Albinism
SS2777611
RM
Clinical Photography, Central Manchester University Hospitals NHS Foundation Trust, UK / Science Source
Occular Albinism
Tay-sachs Disease, illustration
SS2726873
RM
Evan Oto / Science Source
Tay-sachs Disease, illustration
Tay-sachs Disease, Brain Anatomy
SS2726872
RM
Evan Oto / Science Source
Tay-sachs Disease, Brain Anatomy
Albino Burmese Python
SS2569395
RM
Tom McHugh / Science Source
Albino Burmese Python
X-ray of Thalassemia
SS2529049
RM
Biophoto Associates / Science Source
X-ray of Thalassemia
Karyotype, Normal Female Chromosomes
SS2482162
RM
Omikron / Science Source
Karyotype, Normal Female Chromosomes
Karyotype, Normal Female Chromosomes
SS2482161
RM
Omikron / Science Source
Karyotype, Normal Female Chromosomes
Karyotype, Normal Female Chromosomes
SS2482160
RM
Omikron / Science Source
Karyotype, Normal Female Chromosomes
Karyotype, Normal Male Chromosomes
SS2475925
RM
Science Source
Karyotype, Normal Male Chromosomes
Karyotype, Normal Male Chromosomes
SS2475923
RM
Science Source
Karyotype, Normal Male Chromosomes
Karyotype, Normal Male Chromosomes
SS2475922
RM
Science Source
Karyotype, Normal Male Chromosomes
Celiac Disease, LM
SS2441367
RM
Biophoto Associates / Science Source
Celiac Disease, LM
Fragile X Chromosome, Illustration
SS2729808
RM
Monica Schroeder / Science Source
Fragile X Chromosome, Illustration
Personal genetic variants
SS21459202
RM
Martin Shields / Science Source
Personal genetic variants
Karyotype, Normal Female Chromosomes
SS2843019
RM
Omikron / Science Source
Karyotype, Normal Female Chromosomes
Karyotype, Normal Male Chromosomes
SS2843009
RM
Omikron / Science Source
Karyotype, Normal Male Chromosomes
Karyotype, Normal Male Chromosomes
SS2843008
RM
Omikron / Science Source
Karyotype, Normal Male Chromosomes
Karyotype, Normal Male Chromosomes
SS2843006
RM
Omikron / Science Source
Karyotype, Normal Male Chromosomes
Dupuytren's contracture
SS2790347
RM
Clinical Photography, Central Manchester University Hospitals NHS Foundation Trust, UK / Science Source
Dupuytren's contracture
Apert Syndrome
SS2777668
RM
Clinical Photography, Central Manchester University Hospitals NHS Foundation Trust, UK / Science Source
Apert Syndrome
Fragile X Chromosome, Illustration
SS2729844
RM
Monica Schroeder / Science Source
Fragile X Chromosome, Illustration
Fragile X Chromosome, Illustration
SS2729813
RM
Monica Schroeder / Science Source
Fragile X Chromosome, Illustration
Fragile X Chromosome, Illustration
SS2729809
RM
Monica Schroeder / Science Source
Fragile X Chromosome, Illustration
Fragile X Chromosome, Illustration
SS2729802
RM
Monica Schroeder / Science Source
Fragile X Chromosome, Illustration
Tay-sachs Disease, illustration
SS2726871
RM
Evan Oto / Science Source
Tay-sachs Disease, illustration
Tay-sachs Disease, illustration
SS2726870
RM
Evan Oto / Science Source
Tay-sachs Disease, illustration
Tay-sachs Disease, illustration
SS2726869
RM
Evan Oto / Science Source
Tay-sachs Disease, illustration
Normal Female Chromosomes, SKY
SS2700676
RM
NCI/Thomas Ried / Science Source
Normal Female Chromosomes, SKY
Male Karyotype
SS2681086
RM
Spencer Sutton / Science Source
Male Karyotype
Celiac Disease, LM
SS2526255
RM
Biophoto Associates / Science Source
Celiac Disease, LM
Cystic fibrosis
SS2504652
RM
Carol and Mike Werner / Science Source
Cystic fibrosis
Karyotype, Normal Male Chromosomes
SS2482155
RM
Omikron / Science Source
Karyotype, Normal Male Chromosomes
Karyotype, Normal Male Chromosomes
SS2482153
RM
Omikron / Science Source
Karyotype, Normal Male Chromosomes
Karyotype, Normal Female Chromosomes
SS2475946
RM
Biophoto Associates / Science Source
Karyotype, Normal Female Chromosomes
Karyotype, Normal Female Chromosomes
SS2475932
RM
Omikron / Science Source
Karyotype, Normal Female Chromosomes
Karyotype, Normal Male Chromosomes
SS2475928
RM
Omikron / Science Source
Karyotype, Normal Male Chromosomes
Karyotype, Normal Male Chromosomes
SS2475924
RM
Science Source
Karyotype, Normal Male Chromosomes
Pelger-Huet Anomaly (LM)
SS2405760
RM
Garry DeLong / Science Source
Pelger-Huet Anomaly (LM)
Pelger-Huet Anomaly (LM)
SS2405759
RM
Garry DeLong / Science Source
Pelger-Huet Anomaly (LM)
Karyotype, Normal Male Chromosomes
SS2402559
RM
Omikron / Science Source
Karyotype, Normal Male Chromosomes
Karyotype, Normal Male Chromosomes
SS2402558
RM
Omikron / Science Source
Karyotype, Normal Male Chromosomes
Celiac disease, light micrograph
SS2398822
RM
Biophoto Associates / Science Source
Celiac disease, light micrograph
Celiac disease, light micrograph
SS2398821
RM
Biophoto Associates / Science Source
Celiac disease, light micrograph
Karyotype, Normal Female Chromosomes
SS2377527
RM
Biophoto Associates / Science Source
Karyotype, Normal Female Chromosomes
Plaque psoriasis on elbow
SS2294565
RM
Martin Shields / Science Source
Plaque psoriasis on elbow
Plaque psoriasis on leg
SS2294564
RM
Martin Shields / Science Source
Plaque psoriasis on leg
Down's syndrome
SS2143023
RM
Richard Hutchings / Science Source
Down's syndrome
Down Syndrome
SS2143017
RM
Robin Laurance / Science Source
Down Syndrome
Down's Syndrome
SS2137009
RM
Ken Lax / Science Source
Down's Syndrome
Karyotype, Normal Male Chromosomes
SS2105935
RM
Omikron / Science Source
Karyotype, Normal Male Chromosomes
Down Syndrome
SS298593
RM
Bruce Roberts / Science Source
Down Syndrome
Karyotype, Normal Male Chromosomes
SS2482154
RM
Omikron / Science Source
Karyotype, Normal Male Chromosomes
Karyotype, Normal Male Chromosomes
SS2475931
RM
Omikron / Science Source
Karyotype, Normal Male Chromosomes
Karyotype, Normal Male Chromosomes
SS2475930
RM
Omikron / Science Source
Karyotype, Normal Male Chromosomes
Karyotype, Normal Male Chromosomes
SS2475929
RM
Omikron / Science Source
Karyotype, Normal Male Chromosomes
Karyotype, Normal Male Chromosomes
SS2475927
RM
Omikron / Science Source
Karyotype, Normal Male Chromosomes
Woman's hands tied with double helix string
SS21938512
RM
Jens Magnusson / Science Source
Woman's hands tied with double helix string
Personal genetic variants
SS21459201
RM
Martin Shields / Science Source
Personal genetic variants
Macular degeneration gene
SS21459140
RM
Martin Shields / Science Source
Macular degeneration gene
Macular degeneration gene
SS21459139
RM
Martin Shields / Science Source
Macular degeneration gene
APOE gene results
SS21459138
RM
Martin Shields / Science Source
APOE gene results
APOE gene results
SS21459135
RM
Martin Shields / Science Source
APOE gene results
 Hemochromatosis test result
SS21459137
RM
Martin Shields / Science Source
Hemochromatosis test result
 Hemochromatosis test result
SS21459136
RM
Martin Shields / Science Source
Hemochromatosis test result
 Hemochromatosis test result
SS21459073
RM
Martin Shields / Science Source
Hemochromatosis test result
BRCA1/BRCA2 results
SS21459074
RM
Martin Shields / Science Source
BRCA1/BRCA2 results
BRCA1/BRCA2 results
SS21459072
RM
Martin Shields / Science Source
BRCA1/BRCA2 results
BRCA1/BRCA2 results
SS21459071
RM
Martin Shields / Science Source
BRCA1/BRCA2 results
BRCA1/BRCA2 results
SS21459069
RM
Martin Shields / Science Source
BRCA1/BRCA2 results
BRCA1/BRCA2 results
SS21459070
RM
Martin Shields / Science Source
BRCA1/BRCA2 results
Sickle Cell Anemia, Human RBCs, SEM
SS2761183
RM
CDC/Janice Haney Carr / Science Source
Sickle Cell Anemia, Human RBCs, SEM
Sickle Cell Anemia, Human RBCs, SEM
SS2761182
RM
CDC/Janice Haney Carr / Science Source
Sickle Cell Anemia, Human RBCs, SEM
Sickle Cell Anemia, Human RBCs, SEM
SS2761181
RM
CDC/Janice Haney Carr / Science Source
Sickle Cell Anemia, Human RBCs, SEM
Sickle Cell Anemia, Human RBCs, SEM
SS2761180
RM
CDC/Janice Haney Carr / Science Source
Sickle Cell Anemia, Human RBCs, SEM
Sickle Cell Anemia, Human RBCs, SEM
SS2761179
RM
CDC/Janice Haney Carr / Science Source
Sickle Cell Anemia, Human RBCs, SEM
Sickle Cell Anemia, Human RBCs, SEM
SS2761178
RM
CDC/Janice Haney Carr / Science Source
Sickle Cell Anemia, Human RBCs, SEM
Sickle Cell Anemia, Human RBCs, SEM
SS2761177
RM
CDC/Janice Haney Carr / Science Source
Sickle Cell Anemia, Human RBCs, SEM
Sickle Cell Anemia, Human RBCs, SEM
SS2761176
RM
CDC/Janice Haney Carr / Science Source
Sickle Cell Anemia, Human RBCs, SEM
Fragile X Syndrome, Illustration
SS2729812
RM
Monica Schroeder / Science Source
Fragile X Syndrome, Illustration
Fragile X Syndrome, Illustration
SS2729811
RM
Monica Schroeder / Science Source
Fragile X Syndrome, Illustration
Fragile X Syndrome, Illustration
SS2729810
RM
Monica Schroeder / Science Source
Fragile X Syndrome, Illustration
Fragile X Syndrome, Illustration
SS2729807
RM
Monica Schroeder / Science Source
Fragile X Syndrome, Illustration
Fragile X Syndrome, Illustration
SS2729806
RM
Monica Schroeder / Science Source
Fragile X Syndrome, Illustration
Fragile X Syndrome, Illustration
SS2729805
RM
Monica Schroeder / Science Source
Fragile X Syndrome, Illustration
Fragile X Inheritance, Illustration
SS2729804
RM
Monica Schroeder / Science Source
Fragile X Inheritance, Illustration
Fragile X Inheritance, Illustration
SS2729803
RM
Monica Schroeder / Science Source
Fragile X Inheritance, Illustration
Fragile X Inheritance, Illustration
SS2729801
RM
Monica Schroeder / Science Source
Fragile X Inheritance, Illustration
Early Onset AD: DNA, Chromosomes and Genes
SS2727402
RM
National Institute on Aging/NIH / Science Source
Early Onset AD: DNA, Chromosomes and Genes
Breast Cancer, Genetics Research
SS2726875
RM
Ernesto del Aguila III/NHGRI / Science Source
Breast Cancer, Genetics Research
Normal and Abnormal Jejunum (Celiac Disease)
SS2526265
RM
Biophoto Associates / Science Source
Normal and Abnormal Jejunum (Celiac Disease)
Historical Criminal Typing by Class: "Manly and Intelligent"
SS2502413
RM
New York Public Library / Science Source
Historical Criminal Typing by Class: "Manly and Intelligent"
Historical Criminal Typing by Class: "Dullards"
SS2502412
RM
New York Public Library / Science Source
Historical Criminal Typing by Class: "Dullards"
Historical Criminal Typing by Class: "Sexual Perverts"
SS2502410
RM
New York Public Library / Science Source
Historical Criminal Typing by Class: "Sexual Perverts"
Down Syndrome
SS2143019
RM
Lawrence Migdale / Science Source
Down Syndrome
Genetic data connecting male and female profiles
SS22542906
RM
Gary Waters / Science Source
Genetic data connecting male and female profiles
Woman wondering about her ancestry
SS22542442
RM
Bjorn Rune Lie / Science Source
Woman wondering about her ancestry
Mendel's Peas
SS2502487
RM
Spencer Sutton / Science Source
Mendel's Peas
Mendel's Peas
SS2502486
RM
Spencer Sutton / Science Source
Mendel's Peas
Heterochromia Iridum
SS2482272
RF
Gwen Shockey / Science Source
Heterochromia Iridum
Down's Syndrome student
SS298594
RM
Richard Hutchings / Science Source
Down's Syndrome student
Genetic sequence
SS21339574
RM
ALFRED PASIEKA / Science Source
Genetic sequence
Genetic sequence
SS21339573
RM
ALFRED PASIEKA / Science Source
Genetic sequence
Artwork of philosophers sitting and thinking
SS21314483
RM
ANDRZEJ DUDZINSKI / Science Source
Artwork of philosophers sitting and thinking
Blue sclera of eye in osteogenesis imperfecta
SS2755063
RM
James Stevenson / Science Source
Blue sclera of eye in osteogenesis imperfecta
Male karyotype
SS2377799
RM
VĂ©ronique Estiot / Science Source
Male karyotype
Cafe au lait spot
SS2175123
RM
Dr P. Marazzi / Science Source
Cafe au lait spot
Eye color genetics, computer artwork
SS294117
RM
Tim Vernon, LTH NHS Trust / Science Source
Eye color genetics, computer artwork
Accumulation of genetic mutations
SS257563
RM
Francis Leroy & Mayric Huart, Biocosmos/ SPL / Science Source
Accumulation of genetic mutations
Antibody Nomenclature, Illustration
SS2811214
RM
MedicalWriters / Science Source
Antibody Nomenclature, Illustration
Chromosomes
SS21313871
RM
MEHAU KULYK / Science Source
Chromosomes
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