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Search Results for - heritable

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ID
 
Description
 
Product
 
Source
(Showing Items: 50)
 
 
 
 
HUMAN GENE MUTATION PANEL - HEMOCHROMATOSIS
 
gene mutation panel
 
 
 
 
 
HUMAN GENE MUTATION PANEL - DISORDERS OF THROMBOSIS
 
gene mutation panel
 
 
 
 
 
OBESITY
 
DNA
 
LCL
 
 
 
 
OBESITY
 
DNA
 
LCL
 
 
 
 
NIA AGING CELL REPOSITORY DNA PANEL - EARLY ONSET FAMILIAL ALZHEIMER DISEASE
 
aging mapping panel
 
 
 
 
 
NIA AGING CELL REPOSITORY DNA PANEL - CHARACTERIZED MUTATIONS
 
aging mapping panel
 
 
 
 
 
NIA AGING CELL REPOSITORY DNA PANEL - LATE ONSET FAMILIAL ALZHEIMER DISEASE
 
aging mapping panel
 
 
 
 
 
APPARENTLY HEALTHY INDIVIDUAL
 
DNA
 
LCL
 
 
 
 
OBESITY
 
DNA
 
LCL
 
 
 
 
OBESITY
 
DNA
 
LCL
 
 
 
 
OBESITY
 
DNA
 
LCL
 
 
 
 
OBESITY
 
DNA
 
LCL
 
 
 
 
OBESITY
 
DNA
 
LCL
 
 
 
 
OBESITY
 
DNA
 
LCL
 
 
 
 
CYSTIC FIBROSIS; CF
 
Fibroblast
 
 
 
 
 
CEPH/VENEZUELAN PEDIGREE 102
 
DNA
 
LCL
 
 
 
 
TRISOMY 21 | ANEUPLOID CHROMOSOME NUMBER - TRISOMY
 
DNA
 
Fibroblast
 
 
 
 
PROPIONIC ACIDEMIA
 
DNA
 
LCL
 
 
 
 
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA
 
DNA
 
LCL
 
 
 
 
APPARENTLY HEALTHY INDIVIDUAL
 
DNA
 
LCL
 
 
 
 
OSTEOGENESIS IMPERFECTA: GENETICS UNCERTAIN; NON-LETHAL
 
Fibroblast
 
 
 
 
 
CENTRONUCLEAR MYOPATHY - TYPE UNKNOWN
 
LCL
 
B-Lymphocyte
 
 
 
 
EPIDERMOLYSIS BULLOSA: DYSTROPHIC, JUNCTIONAL, OR SIMPLEX TYPES
 
Fibroblast
 
 
 
 
 
OBESITY
 
LCL
 
B-Lymphocyte
 
 
 
 
MACROGLOSSIA
 
Fibroblast
 
 
 
 
 
OBESITY
 
LCL
 
B-Lymphocyte
 
 
 
 
MUCOPOLYSACCHARIDOSIS TYPE IIIA
 
DNA
 
Fibroblast
 
 
 
 
OSTEOGENESIS IMPERFECTA: GENETICS UNCERTAIN; NON-LETHAL
 
Fibroblast
 
 
 
 
 
GLUT1 DEFICIENCY SYNDROME 1; GLUT1DS1
 
LCL
 
B-Lymphocyte
 
 
 
 
DYSTONIA MUSCULORUM DEFORMANS: TYPE UNKNOWN
 
Fibroblast
 
 
 
 
 
OSTEOGENESIS IMPERFECTA: GENETICS UNCERTAIN; LETHAL
 
Fibroblast
 
 
 
 
 
HOLOPROSENCEPHALY
 
LCL
 
B-Lymphocyte
 
 
 
 
TRIOSEPHOSPHATE ISOMERASE DEFICIENCY; TPID
 
Fibroblast
 
 
 
 
 
CYSTIC FIBROSIS; CF
 
DNA
 
Fibroblast
 
 
 
 
EPIDERMOLYSIS BULLOSA: DYSTROPHIC, JUNCTIONAL, OR SIMPLEX TYPES
 
Fibroblast
 
 
 
 
 
XERODERMA PIGMENTOSUM: COMPLEMENTATION GROUP UNDETERMINED
 
DNA
 
Fibroblast
 
 
 
 
PARANA HARD-SKIN SYNDROME
 
Fibroblast
 
 
 
 
 
CEREBRAL CREATINE DEFICIENCY SYNDROME 1; CCDS1
 
Fibroblast
 
Skin, Skin
 
 
 
 
CYSTIC FIBROSIS; CF
 
DNA
 
LCL
 
 
 
 
SITOSTEROLEMIA
 
Fibroblast
 
 
 
 
 
ALLERGIC ASTHMATIC
 
LCL
 
B-Lymphocyte
 
 
 
 
DYSTONIA MUSCULORUM DEFORMANS: TYPE UNKNOWN
 
Fibroblast
 
 
 
 
 
APPARENTLY HEALTHY INDIVIDUAL
 
LCL
 
B-Lymphocyte
 
 
 
 
XERODERMA PIGMENTOSUM: COMPLEMENTATION GROUP UNDETERMINED
 
Fibroblast
 
 
 
 
 
APPARENTLY HEALTHY INDIVIDUAL
 
DNA
 
LCL
 
 
 
 
DYSTONIA MUSCULORUM DEFORMANS: TYPE UNKNOWN
 
Fibroblast
 
 
 
 
 
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA
 
DNA
 
LCL
 
 
 
 
OBESITY
 
LCL
 
B-Lymphocyte
 
 
 
 
SENSORY NEUROPATHY TYPE UNKNOWN
 
Fibroblast
 
 
 
 
 
HUMAN GENE MUTATION PANEL - CYSTIC FIBROSIS (VERSION 2)
 
gene mutation panel
 

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