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Search Results for - GSD V

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Description
 
Product
 
Source
(Showing Items: 50)
 
 
 
 
GLYCOGEN STORAGE DISEASE V
 
DNA
 
Fibroblast
 
 
 
 
GLYCOGEN STORAGE DISEASE V
 
Fibroblast
 
 
 
 
 
GLYCOGEN STORAGE DISEASE V
 
LCL
 
B-Lymphocyte
 
 
 
 
GLYCOGEN STORAGE DISEASE V
 
LCL
 
B-Lymphocyte
 
 
 
 
GLYCOGEN STORAGE DISEASE V | GLYCOGEN PHOSPHORYLASE, MUSCLE; PYGM
 
LCL
 
B-Lymphocyte
 
 
 
 
EPSTEIN BARR VIRUS (EBV)
 
Virus
 
 
 
 
 
GLYCOGEN STORAGE DISEASE VIII (IX, INCLUDED) | EHLERS-DANLOS SYNDROME, TYPE III
 
LCL
 
B-Lymphocyte
 
 
 
 
FACTOR V DEFICIENCY
 
DNA
 
LCL
 
 
 
 
GLYCOGEN STORAGE DISEASE VIII (IX, INCLUDED) | EHLERS-DANLOS SYNDROME, TYPE III | APPARENTLY HEALTHY INDIVIDUAL
 
LCL
 
B-Lymphocyte
 
 
 
 
GERSTMANN-STRAUSSLER DISEASE; GSD
 
LCL
 
B-Lymphocyte
 
 
 
 
GLYCOGEN STORAGE DISEASE VIII (IX, INCLUDED) | EHLERS-DANLOS SYNDROME, TYPE III | APPARENTLY HEALTHY INDIVIDUAL
 
Fibroblast
 
Skin, Thigh
 
 
 
 
GERSTMANN-STRAUSSLER DISEASE; GSD
 
DNA
 
LCL
 
 
 
 
CRICETULUS
 
Fibroblast
 
 
 
 
 
FACTOR V DEFICIENCY | HUMAN GENE MUTATION PANEL - DISORDERS OF THROMBOSIS
 
DNA
 
LCL
 
 
 
 
GLYCOGEN STORAGE DISEASE VIII (IX, INCLUDED) | EHLERS-DANLOS SYNDROME, TYPE III
 
Fibroblast
 
Skin, Thigh
 
 
 
 
GLYCOGEN STORAGE DISEASE VIII (IX, INCLUDED) | EHLERS-DANLOS SYNDROME, TYPE III
 
Fibroblast
 
Skin, Thigh
 
 
 
 
GLYCOGEN STORAGE DISEASE VIII (IX, INCLUDED) | EHLERS-DANLOS SYNDROME, TYPE III
 
LCL
 
B-Lymphocyte
 
 
 
 
GLYCOGEN STORAGE DISEASE VIII (IX, INCLUDED) | EHLERS-DANLOS SYNDROME, TYPE III
 
LCL
 
B-Lymphocyte
 
 
 
 
GLYCOGEN STORAGE DISEASE VIII (IX, INCLUDED) | EHLERS-DANLOS SYNDROME, TYPE III
 
DNA
 
LCL
 
 
 
 
FACTOR V DEFICIENCY
 
LCL
 
B-Lymphocyte
 
 
 
 
GLYCOGEN STORAGE DISEASE VIII (IX, INCLUDED) | EHLERS-DANLOS SYNDROME, TYPE III | APPARENTLY HEALTHY INDIVIDUAL
 
Fibroblast
 
Skin, Thigh
 
 
 
 
GLYCOGEN STORAGE DISEASE VIII (IX, INCLUDED) | EHLERS-DANLOS SYNDROME, TYPE III
 
DNA
 
LCL
 
 
 
 
CRICETULUS
 
Fibroblast
 
 
 
 
 
CRICETULUS
 
Fibroblast
 
 
 
 
 
CRICETULUS
 
Fibroblast
 
 
 
 
 
FACTOR V DEFICIENCY | HUMAN GENE MUTATION PANEL - DISORDERS OF THROMBOSIS
 
LCL
 
B-Lymphocyte
 
 
 
 
CRICETULUS
 
Fibroblast
 
 
 
 
 
CRICETULUS
 
Fibroblast
 
 
 
 
 
CRICETULUS
 
Fibroblast
 
 
 
 
 
GLYCOGEN STORAGE DISEASE VIII (IX, INCLUDED) | EHLERS-DANLOS SYNDROME, TYPE III
 
DNA
 
LCL
 
 
 
 
GLYCOGEN STORAGE DISEASE VIII (IX, INCLUDED) | EHLERS-DANLOS SYNDROME, TYPE III
 
LCL
 
B-Lymphocyte
 
 
 
 
GLYCOGEN STORAGE DISEASE VIII (IX, INCLUDED) | EHLERS-DANLOS SYNDROME, TYPE III
 
Fibroblast
 
Skin, Arm
 
 
 
 
HEMOCHROMATOSIS; HFE | FACTOR V DEFICIENCY
 
DNA
 
LCL
 
 
 
 
REFSUM DISEASE | RETINITIS PIGMENTOSA 1; RP1
 
Fibroblast
 
Skin, Unspecified
 
 
 
 
5,10-@METHYLENETETRAHYDROFOLATE REDUCTASE; MTHFR | FACTOR V DEFICIENCY
 
DNA
 
LCL
 
 
 
 
ERYTHROCYTOSIS, FAMILIAL, 6; ECYT6 | HEMOGLOBIN--BETA LOCUS; HBB | FACTOR V DEFICIENCY
 
DNA
 
LCL
 
 
 
 
EHLERS-DANLOS SYNDROME, TYPE I; EDS1 | COLLAGEN, TYPE V, ALPHA-1; COL5A1
 
LCL
 
B-Lymphocyte
 
 
 
 
EHLERS-DANLOS SYNDROME, TYPE I; EDS1 | COLLAGEN, TYPE V, ALPHA-1; COL5A1
 
DNA
 
LCL
 
 
 
 
EHLERS-DANLOS SYNDROME, TYPE I; EDS1 | COLLAGEN, TYPE V, ALPHA-1; COL5A1
 
LCL
 
B-Lymphocyte
 
 
 
 
GLYCOGEN STORAGE DISEASE VIII (IX, INCLUDED) | EHLERS-DANLOS SYNDROME, TYPE III
 
LCL
 
B-Lymphocyte
 
 
 
 
EHLERS-DANLOS SYNDROME, TYPE II; EDS2 | COLLAGEN, TYPE V, ALPHA-1; COL5A1
 
Fibroblast
 
Skin, Arm
 
 
 
 
HEMOCHROMATOSIS; HFE | FACTOR V DEFICIENCY | HUMAN GENE MUTATION PANEL - HEMOCHROMATOSIS
 
DNA
 
LCL
 
 
 
 
EHLERS-DANLOS SYNDROME, TYPE II; EDS2 | COLLAGEN, TYPE V, ALPHA-1; COL5A1
 
LCL
 
B-Lymphocyte
 
 
 
 
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP E
 
LCL
 
B-Lymphocyte
 
 
 
 
CRICETULUS
 
Fibroblast
 
 
 
 
 
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP E
 
DNA
 
LCL
 
 
 
 
CRICETULUS
 
Fibroblast
 
 
 
 
 
GLYCOGEN STORAGE DISEASE II | GLUCOSIDASE, ALPHA, ACID; GAA
 
Fibroblast
 
Skin, Unspecified
 
 
 
 
GLYCOGEN STORAGE DISEASE II
 
LCL
 
B-Lymphocyte
 
 
 
 
GLYCOGEN STORAGE DISEASE II
 
LCL
 
B-Lymphocyte

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