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Search results for: inherited
Pelger-Huet anomaly, LM
SS21336776
RM
Nature's Faces
Pelger-Huet anomaly, LM
Pelger-Huet anomaly, LM
SS21336630
RM
Nature's Faces
Pelger-Huet anomaly, LM
Pelger-Huet anomaly, LM
SS21336554
RM
Nature's Faces
Pelger-Huet anomaly, LM
Pelger-Huet anomaly, LM
SS21336524
RM
Nature's Faces
Pelger-Huet anomaly, LM
Pelger-Huet anomaly, LM
SS21336523
RM
Nature's Faces
Pelger-Huet anomaly, LM
Hereditary elliptocytosis, LM
SS21335825
RM
Nature's Faces
Hereditary elliptocytosis, LM
Elliptocytosis, LM
SS21337165
RM
Nature's Faces
Elliptocytosis, LM
Hereditary pyropoikilocytosis, LM
SS21335827
RM
Nature's Faces
Hereditary pyropoikilocytosis, LM
Down Syndrome Human Karyotype
SS2871921
JG8056
RM
Wellcome Images
Down Syndrome Human Karyotype
Dupuytren's contracture
SS2790347
JG3334
RM
Clinical Photography, Central Manchester University Hospitals NHS Foundation Trust, UK
Dupuytren's contracture
Occular Albinism
SS2777612
JF7053
RM
Clinical Photography, Central Manchester University Hospitals NHS Foundation Trust, UK
Occular Albinism
Occular Albinism
SS2777611
JF7052
RM
Clinical Photography, Central Manchester University Hospitals NHS Foundation Trust, UK
Occular Albinism
Tay-sachs Disease, illustration
SS2726873
JD4229
RM
Evan Oto
Tay-sachs Disease, illustration
Tay-sachs Disease, Brain Anatomy
SS2726872
JD4227
RM
Evan Oto
Tay-sachs Disease, Brain Anatomy
Tay-sachs Disease, illustration
SS2726871
JD4228
RM
Evan Oto
Tay-sachs Disease, illustration
Albino Burmese Python
SS2569395
4N3136
RM
Tom McHugh
Albino Burmese Python
Karyotype, Normal Female Chromosomes
SS2482162
BU8915
RM
Omikron
Karyotype, Normal Female Chromosomes
Karyotype, Normal Female Chromosomes
SS2482161
BU8914
RM
Omikron
Karyotype, Normal Female Chromosomes
Karyotype, Normal Female Chromosomes
SS2482160
BU8913
RM
Omikron
Karyotype, Normal Female Chromosomes
Karyotype, Normal Male Chromosomes
SS2482154
BU8907
RM
Omikron
Karyotype, Normal Male Chromosomes
Karyotype, Normal Male Chromosomes
SS2475931
BU8905
RM
Omikron
Karyotype, Normal Male Chromosomes
Karyotype, Normal Male Chromosomes
SS2475930
BU8904
RM
Omikron
Karyotype, Normal Male Chromosomes
Karyotype, Normal Male Chromosomes
SS2475929
BU8903
RM
Omikron
Karyotype, Normal Male Chromosomes
Karyotype, Normal Male Chromosomes
SS2475927
BU8901
RM
Omikron
Karyotype, Normal Male Chromosomes
Karyotype, Normal Male Chromosomes
SS2475925
BU8899
RM
Science Source
Karyotype, Normal Male Chromosomes
Karyotype, Normal Male Chromosomes
SS2475923
BU8897
RM
Science Source
Karyotype, Normal Male Chromosomes
Karyotype, Normal Male Chromosomes
SS2475922
BU8896
RM
Science Source
Karyotype, Normal Male Chromosomes
Fragile X Chromosome, Illustration
SS2729808
JD7133
RM
Monica Schroeder
Fragile X Chromosome, Illustration
Personal genetic variants
SS21459202
RM
Martin Shields
Personal genetic variants
 Hemochromatosis test result
SS21459073
RM
Martin Shields
Hemochromatosis test result
Karyotype, Normal Female Chromosomes
SS2843019
9B0914
RM
Omikron
Karyotype, Normal Female Chromosomes
Karyotype, Normal Male Chromosomes
SS2843009
9A6580
RM
Omikron
Karyotype, Normal Male Chromosomes
Karyotype, Normal Male Chromosomes
SS2843008
9A5846
RM
Omikron
Karyotype, Normal Male Chromosomes
Karyotype, Normal Male Chromosomes
SS2843006
9A3161
RM
Omikron
Karyotype, Normal Male Chromosomes
Apert Syndrome
SS2777668
JF7109
RM
Clinical Photography, Central Manchester University Hospitals NHS Foundation Trust, UK
Apert Syndrome
Fragile X Chromosome, Illustration
SS2729844
JD7131
RM
Monica Schroeder
Fragile X Chromosome, Illustration
Fragile X Chromosome, Illustration
SS2729813
JD7132
RM
Monica Schroeder
Fragile X Chromosome, Illustration
Fragile X Chromosome, Illustration
SS2729809
JD7134
RM
Monica Schroeder
Fragile X Chromosome, Illustration
Fragile X Inheritance, Illustration
SS2729804
JD7136
RM
Monica Schroeder
Fragile X Inheritance, Illustration
Fragile X Chromosome, Illustration
SS2729802
JD7135
RM
Monica Schroeder
Fragile X Chromosome, Illustration
Fragile X Inheritance, Illustration
SS2729803
JD7138
RM
Monica Schroeder
Fragile X Inheritance, Illustration
Fragile X Inheritance, Illustration
SS2729801
JD7137
RM
Monica Schroeder
Fragile X Inheritance, Illustration
Tay-sachs Disease, illustration
SS2726870
JD4226
RM
Evan Oto
Tay-sachs Disease, illustration
Tay-sachs Disease, illustration
SS2726869
JD4230
RM
Evan Oto
Tay-sachs Disease, illustration
Normal Female Chromosomes, SKY
SS2700676
JC5130
RM
NCI/Thomas Ried
Normal Female Chromosomes, SKY
Male Karyotype
SS2681086
JB9134
RM
Spencer Sutton
Male Karyotype
Retinitis Pigmentosa
SS2570673
BY2646
RM
Paul Whitten
Retinitis Pigmentosa
Retinitis Pigmentosa
SS2570672
BY2645
RM
Paul Whitten
Retinitis Pigmentosa
Cystic fibrosis
SS2504652
BU6279
RM
Carol and Mike Werner
Cystic fibrosis
Heterochromia Iridum
SS2482272
BU9054
RM
Gwen Shockey
Heterochromia Iridum
Karyotype, Normal Male Chromosomes
SS2482155
BU8908
RM
Omikron
Karyotype, Normal Male Chromosomes
Karyotype, Normal Male Chromosomes
SS2482153
BU8906
RM
Omikron
Karyotype, Normal Male Chromosomes
Karyotype, Normal Female Chromosomes
SS2475932
BU8916
RM
Omikron
Karyotype, Normal Female Chromosomes
Karyotype, Normal Male Chromosomes
SS2475928
BU8902
RM
Omikron
Karyotype, Normal Male Chromosomes
Karyotype, Normal Male Chromosomes
SS2475924
BU8898
RM
Science Source
Karyotype, Normal Male Chromosomes
Pelger-Huet Anomaly (LM)
SS2405760
BQ6866
RM
Garry DeLong
Pelger-Huet Anomaly (LM)
Pelger-Huet Anomaly (LM)
SS2405759
BQ6865
RM
Garry DeLong
Pelger-Huet Anomaly (LM)
Karyotype, Normal Male Chromosomes
SS2402559
BQ3377
RM
Omikron
Karyotype, Normal Male Chromosomes
Karyotype, Normal Male Chromosomes
SS2402558
BQ3376
RM
Omikron
Karyotype, Normal Male Chromosomes
Plaque psoriasis on elbow
SS2294565
BG0539
RM
Martin Shields
Plaque psoriasis on elbow
Plaque psoriasis on leg
SS2294564
BG0538
RM
Martin Shields
Plaque psoriasis on leg
Down's syndrome
SS2143023
5P8695
RM
Richard Hutchings
Down's syndrome
Down Syndrome
SS2143019
3H5549
RM
Lawrence Migdale
Down Syndrome
Down Syndrome
SS2143017
2D1875
RM
Robin Laurance
Down Syndrome
Down's Syndrome
SS2137009
3L5269
RM
Ken Lax
Down's Syndrome
Karyotype, Normal Male Chromosomes
SS2105935
5R8072
RM
Omikron
Karyotype, Normal Male Chromosomes
Down Syndrome
SS298593
6A6702
RM
Bruce Roberts
Down Syndrome
Woman's hands tied with double helix string
SS21938512
RM
Jens Magnusson
Woman's hands tied with double helix string
Personal genetic variants
SS21459201
RM
Martin Shields
Personal genetic variants
Macular degeneration gene
SS21459140
RM
Martin Shields
Macular degeneration gene
Macular degeneration gene
SS21459139
RM
Martin Shields
Macular degeneration gene
APOE gene results
SS21459138
RM
Martin Shields
APOE gene results
APOE gene results
SS21459135
RM
Martin Shields
APOE gene results
 Hemochromatosis test result
SS21459137
RM
Martin Shields
Hemochromatosis test result
 Hemochromatosis test result
SS21459136
RM
Martin Shields
Hemochromatosis test result
BRCA1/BRCA2 results
SS21459074
RM
Martin Shields
BRCA1/BRCA2 results
BRCA1/BRCA2 results
SS21459072
RM
Martin Shields
BRCA1/BRCA2 results
BRCA1/BRCA2 results
SS21459071
RM
Martin Shields
BRCA1/BRCA2 results
BRCA1/BRCA2 results
SS21459069
RM
Martin Shields
BRCA1/BRCA2 results
BRCA1/BRCA2 results
SS21459070
RM
Martin Shields
BRCA1/BRCA2 results
Sickle Cell Anemia, Human RBCs, SEM
SS2761183
JF0517
RM
CDC/Janice Haney Carr
Sickle Cell Anemia, Human RBCs, SEM
Sickle Cell Anemia, Human RBCs, SEM
SS2761182
JF0518
RM
CDC/Janice Haney Carr
Sickle Cell Anemia, Human RBCs, SEM
Sickle Cell Anemia, Human RBCs, SEM
SS2761181
JF0515
RM
CDC/Janice Haney Carr
Sickle Cell Anemia, Human RBCs, SEM
Sickle Cell Anemia, Human RBCs, SEM
SS2761180
JF0516
RM
CDC/Janice Haney Carr
Sickle Cell Anemia, Human RBCs, SEM
Sickle Cell Anemia, Human RBCs, SEM
SS2761179
JF0513
RM
CDC/Janice Haney Carr
Sickle Cell Anemia, Human RBCs, SEM
Sickle Cell Anemia, Human RBCs, SEM
SS2761178
JF0514
RM
CDC/Janice Haney Carr
Sickle Cell Anemia, Human RBCs, SEM
Sickle Cell Anemia, Human RBCs, SEM
SS2761177
JF0511
RM
CDC/Janice Haney Carr
Sickle Cell Anemia, Human RBCs, SEM
Sickle Cell Anemia, Human RBCs, SEM
SS2761176
JF0512
RM
CDC/Janice Haney Carr
Sickle Cell Anemia, Human RBCs, SEM
Fragile X Syndrome, Illustration
SS2729812
JD7142
RM
Monica Schroeder
Fragile X Syndrome, Illustration
Fragile X Syndrome, Illustration
SS2729811
JD7143
RM
Monica Schroeder
Fragile X Syndrome, Illustration
Fragile X Syndrome, Illustration
SS2729810
JD7144
RM
Monica Schroeder
Fragile X Syndrome, Illustration
Fragile X Syndrome, Illustration
SS2729807
JD7141
RM
Monica Schroeder
Fragile X Syndrome, Illustration
Fragile X Syndrome, Illustration
SS2729806
JD7140
RM
Monica Schroeder
Fragile X Syndrome, Illustration
Fragile X Syndrome, Illustration
SS2729805
JD7139
RM
Monica Schroeder
Fragile X Syndrome, Illustration
Early Onset AD: DNA, Chromosomes and Genes
SS2727402
JD3495
RM
National Institute on Aging/NIH
Early Onset AD: DNA, Chromosomes and Genes
Breast Cancer, Genetics Research
SS2726875
JD3448
RM
Ernesto del Aguila III/NHGRI
Breast Cancer, Genetics Research
Mendel's Peas
SS2502487
BU5187
RM
Spencer Sutton
Mendel's Peas
Mendel's Peas
SS2502486
BU5186
RM
Spencer Sutton
Mendel's Peas
Historical Criminal Typing by Class: "Manly and Intelligent"
SS2502413
BU3978
RM
New York Public Library
Historical Criminal Typing by Class: "Manly and Intelligent"
Historical Criminal Typing by Class: "Dullards"
SS2502412
BU3977
RM
New York Public Library
Historical Criminal Typing by Class: "Dullards"
Historical Criminal Typing by Class: "Sexual Perverts"
SS2502410
BU3976
RM
New York Public Library
Historical Criminal Typing by Class: "Sexual Perverts"
Genetic sequence
SS21339574
RM
ALFRED PASIEKA
Genetic sequence
Genetic sequence
SS21339573
RM
ALFRED PASIEKA
Genetic sequence
Artwork of philosophers sitting and thinking
SS21314483
RM
ANDRZEJ DUDZINSKI
Artwork of philosophers sitting and thinking
Blue sclera of eye in osteogenesis imperfecta
SS2755063
ST8766
RM
James Stevenson
Blue sclera of eye in osteogenesis imperfecta
Male karyotype
SS2377799
D0428
RM
VĂ©ronique Estiot
Male karyotype
Cafe au lait spot
SS2175123
SC9852
RM
Dr P. Marazzi
Cafe au lait spot
Eye color genetics, computer artwork
SS294117
SB6469
RM
Tim Vernon, LTH NHS Trust
Eye color genetics, computer artwork
Down's Syndrome student
SS298594
6E3030
RM
Richard Hutchings
Down's Syndrome student
X-ray of Thalassemia
SS2529049
9E2533
RM
Biophoto Associates
X-ray of Thalassemia
Chromosomes
SS21313871
RM
MEHAU KULYK
Chromosomes
Chromosomes
SS21313874
RM
MEHAU KULYK
Chromosomes
Chromosomes
SS21313872
RM
MEHAU KULYK
Chromosomes
Chromosomes
SS21313873
RM
MEHAU KULYK
Chromosomes
Chromosomes
SS21313870
RM
MEHAU KULYK
Chromosomes
Chromosome
SS21313875
RM
MEHAU KULYK
Chromosome
Chromosomes
SS21313868
RM
MEHAU KULYK
Chromosomes
Chromosomes
SS21313867
RM
MEHAU KULYK
Chromosomes
Chromosome
SS21313866
RM
MEHAU KULYK
Chromosome
Chromosomes
SS21313865
RM
ALFRED PASIEKA
Chromosomes
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