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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
 
 
 
 
 
APPARENTLY HEALTHY INDIVIDUAL
 
DNA
 
LCL
 
 
 
 
OBESITY
 
DNA
 
LCL
 
 
 
 
OBESITY
 
DNA
 
LCL
 
 
 
 
OBESITY
 
DNA
 
LCL
 
 
 
 
OBESITY
 
DNA
 
LCL
 
 
 
 
OBESITY
 
DNA
 
LCL
 
 
 
 
OBESITY
 
DNA
 
LCL
 
 
 
 
OBESITY
 
DNA
 
LCL
 
 
 
 
OBESITY
 
DNA
 
LCL
 
 
 
 
CYSTIC FIBROSIS; CF
 
LCL
 
B-Lymphocyte
 
 
 
 
RETT SYNDROME, CONGENITAL VARIANT
 
LCL
 
B-Lymphocyte
 
 
 
 
EOSINOPHILIC FASCITIS
 
Fibroblast
 
 
 
 
 
OBESITY
 
LCL
 
B-Lymphocyte
 
 
 
 
OBESITY
 
DNA
 
LCL
 
 
 
 
PROPIONIC ACIDEMIA
 
DNA
 
Fibroblast
 
 
 
 
OBESITY
 
LCL
 
B-Lymphocyte
 
 
 
 
RETT SYNDROME; RTT
 
DNA
 
LCL
 
 
 
 
CENTRONUCLEAR MYOPATHY - TYPE UNKNOWN
 
LCL
 
B-Lymphocyte
 
 
 
 
ALLERGIC ASTHMATIC
 
LCL
 
B-Lymphocyte
 
 
 
 
PROPIONIC ACIDEMIA
 
DNA
 
LCL
 
 
 
 
LESCH-NYHAN SYNDROME; LNS
 
Fibroblast
 
 
 
 
 
CYSTIC FIBROSIS; CF
 
LCL
 
B-Lymphocyte
 
 
 
 
CYSTIC FIBROSIS; CF
 
Fibroblast
 
 
 
 
 
DYSTONIA MUSCULORUM DEFORMANS: TYPE UNKNOWN
 
Fibroblast
 
 
 
 
 
OSTEOGENESIS IMPERFECTA: GENETICS UNCERTAIN; NON-LETHAL
 
Fibroblast
 
 
 
 
 
APPARENTLY HEALTHY INDIVIDUAL
 
LCL
 
B-Lymphocyte
 
 
 
 
MACROGLOSSIA
 
Fibroblast
 
 
 
 
 
PARANA HARD-SKIN SYNDROME
 
Fibroblast
 
 
 
 
 
CEPH/VENEZUELAN PEDIGREE 102
 
DNA
 
LCL
 
 
 
 
CYSTIC FIBROSIS; CF
 
DNA
 
Fibroblast
 
 
 
 
DYSTONIA MUSCULORUM DEFORMANS: TYPE UNKNOWN
 
Fibroblast
 
 
 
 
 
DYSTONIA MUSCULORUM DEFORMANS: TYPE UNKNOWN
 
Fibroblast
 
 
 
 
 
CYSTIC FIBROSIS; CF
 
Fibroblast
 
 
 
 
 
CYSTIC FIBROSIS; CF
 
Fibroblast
 
 
 
 
 
HOLOPROSENCEPHALY
 
LCL
 
B-Lymphocyte
 
 
 
 
DYSTONIA MUSCULORUM DEFORMANS: TYPE UNKNOWN
 
Fibroblast
 
 
 
 
 
HYPER IGM, TYPE UNKNOWN
 
LCL
 
B-Lymphocyte
 
 
 
 
OSTEOGENESIS IMPERFECTA: GENETICS UNCERTAIN; NON-LETHAL
 
Fibroblast
 
 
 
 
 
OSTEOGENESIS IMPERFECTA: GENETICS UNCERTAIN; LETHAL
 
Fibroblast
 
 
 
 
 
OBESITY
 
DNA
 
LCL
 
 
 
 
OBESITY
 
DNA
 
LCL
 
 
 
 
EPIDERMOLYSIS BULLOSA: DYSTROPHIC, JUNCTIONAL, OR SIMPLEX TYPES
 
LCL
 
B-Lymphocyte
 
 
 
 
TRIOSEPHOSPHATE ISOMERASE DEFICIENCY; TPID
 
Fibroblast
 
 
 
 
 
SITOSTEROLEMIA
 
Fibroblast
 
 
 
 
 
RETT SYNDROME, CONGENITAL VARIANT
 
Fibroblast
 
Skin, Skin
 
 
 
 
APPARENTLY HEALTHY INDIVIDUAL
 
LCL
 
B-Lymphocyte
 
 
 
 
TUBEROUS SCLEROSIS 2; TSC2
 
DNA
 
LCL
 
 
 
 
OBESITY
 
DNA
 
LCL

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