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Search Results for - WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, FKTN-RELATED

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1 - 50 of 44830 Results
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ID
 
Description
 
Product
 
Source
(Showing Items: 50)
 
 
 
 
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, 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, 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)
 
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)
 
DNA
 
LCL
 
 
 
 
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, 6; MDDGA6 (WALKER-WARBURG SYNDROME INCLUDED) | CHROMOSOME DELETION | ACETYLGLUCOSAMINYLTRANSFERASE-LIKE PROTEIN; LARGE1
 
Fibroblast
 
Skin, Unspecified
 
 
 
 
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3 | PROTEIN O-MANNOSE BETA-1,2-N-ACETYLGLUCOSAMINYLTRANSFERASE; POMGNT1
 
DNA
 
LCL
 
 
 
 
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3 | PROTEIN O-MANNOSE BETA-1,2-N-ACETYLGLUCOSAMINYLTRANSFERASE; POMGNT1
 
LCL
 
B-Lymphocyte
 
 
 
 
DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, BASAL GANGLIA DISEASE, AND SEIZURES
 
LCL
 
B-Lymphocyte
 
 
 
 
DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, BASAL GANGLIA DISEASE, AND SEIZURES
 
DNA
 
LCL
 
 
 
 
DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, BASAL GANGLIA DISEASE, AND SEIZURES
 
LCL
 
B-Lymphocyte
 
 
 
 
DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, BASAL GANGLIA DISEASE, AND SEIZURES
 
LCL
 
B-Lymphocyte
 
 
 
 
DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, BASAL GANGLIA DISEASE, AND SEIZURES
 
LCL
 
B-Lymphocyte
 
 
 
 
DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, BASAL GANGLIA DISEASE, AND SEIZURES
 
DNA
 
LCL
 
 
 
 
DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, BASAL GANGLIA DISEASE, AND SEIZURES
 
LCL
 
B-Lymphocyte
 
 
 
 
DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, BASAL GANGLIA DISEASE, AND SEIZURES
 
LCL
 
B-Lymphocyte
 
 
 
 
DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, BASAL GANGLIA DISEASE, AND SEIZURES
 
LCL
 
B-Lymphocyte
 
 
 
 
DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, BASAL GANGLIA DISEASE, AND SEIZURES
 
LCL
 
B-Lymphocyte
 
 
 
 
DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, BASAL GANGLIA DISEASE, AND SEIZURES
 
LCL
 
B-Lymphocyte
 
 
 
 
DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, BASAL GANGLIA DISEASE, AND SEIZURES
 
LCL
 
B-Lymphocyte
 
 
 
 
DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, BASAL GANGLIA DISEASE, AND SEIZURES
 
LCL
 
B-Lymphocyte
 
 
 
 
DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, BASAL GANGLIA DISEASE, AND SEIZURES
 
LCL
 
B-Lymphocyte
 
 
 
 
DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, BASAL GANGLIA DISEASE, AND SEIZURES
 
LCL
 
B-Lymphocyte
 
 
 
 
DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, BASAL GANGLIA DISEASE, AND SEIZURES
 
LCL
 
B-Lymphocyte
 
 
 
 
DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, BASAL GANGLIA DISEASE, AND SEIZURES
 
LCL
 
B-Lymphocyte
 
 
 
 
DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, BASAL GANGLIA DISEASE, AND SEIZURES
 
LCL
 
B-Lymphocyte
 
 
 
 
DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, BASAL GANGLIA DISEASE, AND SEIZURES
 
LCL
 
B-Lymphocyte
 
 
 
 
DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, BASAL GANGLIA DISEASE, AND SEIZURES
 
LCL
 
B-Lymphocyte
 
 
 
 
DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, BASAL GANGLIA DISEASE, AND SEIZURES
 
LCL
 
B-Lymphocyte
 
 
 
 
DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, BASAL GANGLIA DISEASE, AND SEIZURES
 
LCL
 
B-Lymphocyte
 
 
 
 
DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, BASAL GANGLIA DISEASE, AND SEIZURES
 
LCL
 
B-Lymphocyte
 
 
 
 
POTOCKI-LUPSKI SYNDROME; PTLS | CHARCOT-MARIE-TOOTH DISEASE, TYPE 1A; CMT1A
 
DNA
 
LCL
 
 
 
 
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7 | ISOPRENOID SYNTHASE DOMAIN-CONTAINING PROTEIN; ISPD
 
Fibroblast
 
Skin, Skin
 
 
 
 
MITOCHONDRIAL MYOPATHY
 
LCL
 
B-Lymphocyte
 
 
 
 
PITT-HOPKINS SYNDROME; PTHS
 
DNA
 
LCL
 
 
 
 
PITT-HOPKINS SYNDROME; PTHS
 
LCL
 
B-Lymphocyte
 
 
 
 
POTOCKI-LUPSKI SYNDROME; PTLS | CHARCOT-MARIE-TOOTH DISEASE, TYPE 1A; CMT1A
 
LCL
 
B-Lymphocyte
 
 
 
 
COCKAYNE SYNDROME TYPE UNSPECIFIED
 
Fibroblast
 
Skin, Unspecified
 
 
 
 
PERSONAL GENOME PROJECT
 
LCL
 
B-Lymphocyte
 
 
 
 
PERSONAL GENOME PROJECT
 
LCL
 
B-Lymphocyte
 
 
 
 
ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD1
 
LCL
 
B-Lymphocyte
 
 
 
 
SEA-BLUE HISTIOCYTE DISEASE
 
LCL
 
B-Lymphocyte
 
 
 
 
SEA-BLUE HISTIOCYTE DISEASE
 
Fibroblast
 

No Results were Found

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