525-00154
Familial dysplastic nevus Skin x80
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525-00154
Familial dysplastic nevus Skin x80
525-00155
Familial dysplastic nevus Skin x80
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525-00155
Familial dysplastic nevus Skin x80
525-00156
Familial dysplastic nevus Skin x200
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525-00156
Familial dysplastic nevus Skin x200
525-00157
Familial dysplastic nevus Skin x200 Color Enhanced
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525-00157
Familial dysplastic nevus Skin x200 Color Enhanced
349-00155
3D Artwork Abnornal RBC, Elliptocyte
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349-00155
3D Artwork Abnornal RBC, Elliptocyte
349-00169
3D Artwork Abnornal RBC, Elliptocyte
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349-00169
3D Artwork Abnornal RBC, Elliptocyte
360-00583
RETINITIS PIGMENTOSA DEGENERATION OF RETINA
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360-00583
RETINITIS PIGMENTOSA DEGENERATION OF RETINA
360-00584
RETINITIS PIGMENTOSA DEGENERATION OF RETINA
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360-00584
RETINITIS PIGMENTOSA DEGENERATION OF RETINA
156-02322
Niemann-Pick disease, Liver tissue section Micrograph
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156-02322
Niemann-Pick disease, Liver tissue section Micrograph
038-00266
Eczema
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038-00266
Eczema
038-00268
Eczema
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038-00268
Eczema
038-00108
Rare disease Neurofibroma associated neuroma
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038-00108
Rare disease Neurofibroma associated neuroma
038-00109
Rare disease Neurofibroma associated neuroma
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038-00109
Rare disease Neurofibroma associated neuroma
313-03753
XRAY OSTEOGENESIS LEGS IMPERFECTA INFANT X RAY
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313-03753
XRAY OSTEOGENESIS LEGS IMPERFECTA INFANT X RAY
366-00868
STATUE SIMON BOLIVAR PARIS FRANCE REBEL LEADER PERU
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366-00868
STATUE SIMON BOLIVAR PARIS FRANCE REBEL LEADER PERU
195-08066
PHOTOMICROGRAPH SICKLE CELL DISEASE RBC GENES
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195-08066
PHOTOMICROGRAPH SICKLE CELL DISEASE RBC GENES
195-08067
PHOTOMICROGRAPH SICKLE CELL DISEASE RBC GENES
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195-08067
PHOTOMICROGRAPH SICKLE CELL DISEASE RBC GENES
195-08069
TRIPLE X SYNDROME X40 PHOTOMICROGRAPH
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195-08069
TRIPLE X SYNDROME X40 PHOTOMICROGRAPH
600-02264
CHARLES V EMPEROR BORN IN FLANDERS RULED EUROPE
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600-02264
CHARLES V EMPEROR BORN IN FLANDERS RULED EUROPE
377-00001
SICKLE CELL ANEMIA BLOOD INHERITED DISORDER BLACK
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377-00001
SICKLE CELL ANEMIA BLOOD INHERITED DISORDER BLACK
366-00245
HALLUX VALGUS FEMALE AFTER BUNIONECTOMY GENETIC
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366-00245
HALLUX VALGUS FEMALE AFTER BUNIONECTOMY GENETIC
366-00246
HALLUX VALGUS FEMALE AFTER BUNIONECTOMY GENETIC
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366-00246
HALLUX VALGUS FEMALE AFTER BUNIONECTOMY GENETIC
366-00247
HALLUX VALGUS FEMALE AFTER BUNIONECTOMY CORRECTIVE
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366-00247
HALLUX VALGUS FEMALE AFTER BUNIONECTOMY CORRECTIVE
366-00248
HALLUX VALGUS FEMALE AFTER BUNNIONECTOMY CORRECTIVE
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366-00248
HALLUX VALGUS FEMALE AFTER BUNNIONECTOMY CORRECTIVE
366-00249
HALLUX VALGUS LEFT PRE RIGHT POST BUNIONECTOMY
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366-00249
HALLUX VALGUS LEFT PRE RIGHT POST BUNIONECTOMY
157-00117
ICHTHYSOSIS INHERITED DISEASE GENETIC DISORDER
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157-00117
ICHTHYSOSIS INHERITED DISEASE GENETIC DISORDER
157-00121
KERATOSIS DIFFUSA FOETALIS ICHTHYOSIS GENETIC SCALE
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157-00121
KERATOSIS DIFFUSA FOETALIS ICHTHYOSIS GENETIC SCALE
157-00122
KERATOSIS FOLLICULARIS DARIER DISEASE GENODERMATO
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157-00122
KERATOSIS FOLLICULARIS DARIER DISEASE GENODERMATO
353-05368
NORMAL AND SICKLE BLOOD CELLS CHART COMPARISON
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353-05368
NORMAL AND SICKLE BLOOD CELLS CHART COMPARISON
313-03661
ICHTHYOSIS RARE CONDITION DISEASE DRY EPIDERMIS
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313-03661
ICHTHYOSIS RARE CONDITION DISEASE DRY EPIDERMIS
195-07495
MEASURING HAIR LOSS MALE TECHNIAN & PATIENT
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195-07495
MEASURING HAIR LOSS MALE TECHNIAN & PATIENT
181-00275
DENTINOGENESIS IMPERFECTA CONGENITAL DISEASE
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181-00275
DENTINOGENESIS IMPERFECTA CONGENITAL DISEASE
181-00276
DENTINOGENESIS IMPERFECTA CONGENITAL DISEASE
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181-00276
DENTINOGENESIS IMPERFECTA CONGENITAL DISEASE
181-00277
DENTINOGENESIS IMPERFECTA CONGENITAL DISEASE
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181-00277
DENTINOGENESIS IMPERFECTA CONGENITAL DISEASE
035-00943
SICKLE CELL - ANEMIA DISFORMED RED BLOOD CELL
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035-00943
SICKLE CELL - ANEMIA DISFORMED RED BLOOD CELL
035-00931
SICKLE CELL MAG X650 INHERITED ANEMIA
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035-00931
SICKLE CELL MAG X650 INHERITED ANEMIA
249-00043
CYSTIC FIBROSIS ILLUSTRATION
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249-00043
CYSTIC FIBROSIS ILLUSTRATION
274-00004
YOUNG WOMAN ROLLING TONGUE INHERITED TRAIT.
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274-00004
YOUNG WOMAN ROLLING TONGUE INHERITED TRAIT.
220-00366
CULTURED CHROMOSOMES FRAGILE X CHROMOSOME
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220-00366
CULTURED CHROMOSOMES FRAGILE X CHROMOSOME
220-00158
KIDNEY, POLYCYSTIC DISEASE X.S. OF INFANTILE KIDNEY
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220-00158
KIDNEY, POLYCYSTIC DISEASE X.S. OF INFANTILE KIDNEY
500-13820
MARFAN'S SYNDROME CLOSEUP OF EYE
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500-13820
MARFAN'S SYNDROME CLOSEUP OF EYE
093-00017
SPASTIC CHILD FROM BOOK BY DR.WILLIAM J. LITTLE
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093-00017
SPASTIC CHILD FROM BOOK BY DR.WILLIAM J. LITTLE