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Search Results for - CEREBROOCULAR DYSPLASIA-MUSCULAR DYSTROPHY SYNDROME

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Description
 
Product
 
Source
(Showing Items: 50)
 
 
 
 
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 1; MDDGA1 (WALKER-WARBURG SYNDROME INCLUDED)
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 1; MDDGA1 (WALKER-WARBURG SYNDROME INCLUDED)
 
DNA
 
LCL
 
 
 
 
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 1; MDDGA1 (WALKER-WARBURG SYNDROME INCLUDED)
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 1; MDDGA1 (WALKER-WARBURG SYNDROME INCLUDED)
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 1; MDDGA1 (WALKER-WARBURG SYNDROME INCLUDED)
 
DNA
 
LCL
 
 
 
 
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 1; MDDGA1 (WALKER-WARBURG SYNDROME INCLUDED)
 
DNA
 
LCL
 
 
 
 
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4 (WALKER-WARBURG SYNDROME INCLUDED) | FUKUTIN; FKTN
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6; MDDGA6 (WALKER-WARBURG SYNDROME INCLUDED) | CHROMOSOME DELETION | ACETYLGLUCOSAMINYLTRANSFERASE-LIKE PROTEIN; LARGE1
 
DNA
 
Fibroblast
 
 
 
 
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4 (WALKER-WARBURG SYNDROME INCLUDED) | FUKUTIN; FKTN
 
Fibroblast
 
 
 
 
 
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4 (WALKER-WARBURG SYNDROME INCLUDED) | FUKUTIN; FKTN
 
DNA
 
Fibroblast
 
 
 
 
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6; MDDGA6 (WALKER-WARBURG SYNDROME INCLUDED) | CHROMOSOME DELETION | ACETYLGLUCOSAMINYLTRANSFERASE-LIKE PROTEIN; LARGE1
 
Fibroblast
 
Skin, Unspecified
 
 
 
 
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1 | TURNER SYNDROME
 
LCL
 
B-Lymphocyte
 
 
 
 
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1 | TURNER SYNDROME
 
DNA
 
LCL
 
 
 
 
ASPHYXIATING THORACIC DYSTROPHY; ATD
 
Fibroblast
 
 
 
 
 
ASPHYXIATING THORACIC DYSTROPHY; ATD
 
Fibroblast
 
 
 
 
 
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1
 
LCL
 
B-Lymphocyte
 
 
 
 
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1
 
LCL
 
B-Lymphocyte
 
 
 
 
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1
 
LCL
 
B-Lymphocyte
 
 
 
 
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1
 
LCL
 
B-Lymphocyte
 
 
 
 
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1
 
LCL
 
B-Lymphocyte
 
 
 
 
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1
 
LCL
 
B-Lymphocyte
 
 
 
 
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1
 
DNA
 
LCL
 
 
 
 
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1
 
DNA
 
LCL
 
 
 
 
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1
 
DNA
 
LCL
 
 
 
 
EMERY-DREIFUSS MUSCULAR DYSTROPHY, 1; EDMD1 | EMERIN; EMD
 
DNA
 
LCL
 
 
 
 
EMERY-DREIFUSS MUSCULAR DYSTROPHY, 1; EDMD1 | EMERIN; EMD
 
LCL
 
B-Lymphocyte
 
 
 
 
EMERY-DREIFUSS MUSCULAR DYSTROPHY, 1; EDMD1 | EMERIN; EMD
 
DNA
 
LCL
 
 
 
 
EMERY-DREIFUSS MUSCULAR DYSTROPHY, 1; EDMD1 | EMERIN; EMD
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2A; LGMD2A
 
Fibroblast
 
 
 
 
 
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2A; LGMD2A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD
 
Fibroblast
 
Skin, Unspecified
 
 
 
 
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2A; LGMD2A
 
DNA
 
LCL
 
 
 
 
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1 | APPARENTLY HEALTHY INDIVIDUAL
 
LCL
 
B-Lymphocyte
 
 
 
 
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1 | APPARENTLY HEALTHY INDIVIDUAL
 
LCL
 
B-Lymphocyte
 
 
 
 
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1
 
LCL
 
B-Lymphocyte
 
 
 
 
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1 | FSHD GENE 1; FRG1
 
DNA
 
LCL
 
 
 
 
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1 | FSHD GENE 1; FRG1
 
DNA
 
LCL
 
 
 
 
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; TYPE UNKNOWN (FSHD)
 
Fibroblast
 
Skin, Unspecified
 
 
 
 
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1 | FSHD GENE 1; FRG1
 
DNA
 
LCL
 
 
 
 
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B; LGMD2B
 
LCL
 
B-Lymphocyte
 
 
 
 
EMERY-DREIFUSS MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT; EDMD2
 
LCL
 
B-Lymphocyte
 
 
 
 
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1 | FSHD GENE 1; FRG1
 
DNA
 
LCL
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
Fibroblast
 
Skin, Unspecified
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
SELENON-RELATED MYOPATHY; RIGID SPINE MUSCULAR DYSTROPHY 1; RSMD1
 
LCL
 
B-Lymphocyte
 
 
 
 
ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD1
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
Fibroblast
 
Skin, Unspecified
 
 
 
 
SELENON-RELATED MYOPATHY; RIGID SPINE MUSCULAR DYSTROPHY 1; RSMD1
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD | CHRONIC GRANULOMATOUS DISEASE (XK-RELATED; CGD) - 306400 OR 314850 | DYSTROPHIN; DMD
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD
 
DNA
 
LCL

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