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ID
 
Description
 
Product
 
Source
(Showing Items: 35)
 
 
 
 
SALLA DISEASE | SOLUTE CARRIER FAMILY 17, MEMBER 5; SLC17A5
 
LCL
 
B-Lymphocyte
 
 
 
 
SALLA DISEASE | SOLUTE CARRIER FAMILY 17, MEMBER 5; SLC17A5
 
DNA
 
LCL
 
 
 
 
SALLA DISEASE | SOLUTE CARRIER FAMILY 17, MEMBER 5; SLC17A5
 
DNA
 
LCL
 
 
 
 
SALLA DISEASE | SOLUTE CARRIER FAMILY 17, MEMBER 5; SLC17A5
 
DNA
 
LCL
 
 
 
 
SALLA DISEASE | SOLUTE CARRIER FAMILY 17, MEMBER 5; SLC17A5
 
LCL
 
B-Lymphocyte
 
 
 
 
SALLA DISEASE | SOLUTE CARRIER FAMILY 17, MEMBER 5; SLC17A5
 
LCL
 
B-Lymphocyte
 
 
 
 
SIALIC ACID STORAGE DISEASE; SIASD
 
Fibroblast
 
 
 
 
 
SIALIC ACID STORAGE DISEASE; SIASD
 
Fibroblast
 
 
 
 
 
SIALIC ACID STORAGE DISEASE; SIASD
 
LCL
 
B-Lymphocyte
 
 
 
 
SIALIC ACID STORAGE DISEASE; SIASD
 
LCL
 
B-Lymphocyte
 
 
 
 
SIALIC ACID STORAGE DISEASE; SIASD
 
Fibroblast
 
 
 
 
 
SIALIC ACID STORAGE DISEASE; SIASD
 
Fibroblast
 
 
 
 
 
SIALIC ACID STORAGE DISEASE; SIASD
 
Fibroblast
 
 
 
 
 
SIALIC ACID STORAGE DISEASE; SIASD
 
Fibroblast
 
 
 
 
 
SIALIC ACID STORAGE DISEASE; SIASD
 
Fibroblast
 
 
 
 
 
SIALIC ACID STORAGE DISEASE; SIASD
 
Fibroblast
 
 
 
 
 
SIALIC ACID STORAGE DISEASE; SIASD
 
Fibroblast
 
 
 
 
 
DUPLICATED CHROMOSOME
 
DNA
 
LCL
 
 
 
 
LANGER MESOMELIC DYSPLASIA | SHORT STATURE HOMEOBOX; SHOX
 
DNA
 
LCL
 
 
 
 
DUPLICATED CHROMOSOME
 
LCL
 
B-Lymphocyte
 
 
 
 
SECKEL SYNDROME | ATAXIA-TELANGIECTASIA AND RAD3-RELATED; ATR
 
DNA
 
Fibroblast
 
 
 
 
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD | TRICHOTHIODYSTROPHY; TTD ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH RETARDATION, INCLUDED | EXCISION-REPAIR, COMPLEMENTING DEFECTIVE, IN CHINESE HAMSTER, 2; ERCC2
 
Fibroblast
 
 
 
 
 
LANGER MESOMELIC DYSPLASIA | SHORT STATURE HOMEOBOX; SHOX
 
LCL
 
B-Lymphocyte
 
 
 
 
SECKEL SYNDROME | ATAXIA-TELANGIECTASIA AND RAD3-RELATED; ATR
 
Fibroblast
 
 
 
 
 
LANGER MESOMELIC DYSPLASIA | SHORT STATURE HOMEOBOX; SHOX
 
DNA
 
LCL
 
 
 
 
LANGER MESOMELIC DYSPLASIA | SHORT STATURE HOMEOBOX; SHOX
 
DNA
 
LCL
 
 
 
 
LANGER MESOMELIC DYSPLASIA | SHORT STATURE HOMEOBOX; SHOX
 
DNA
 
LCL
 
 
 
 
LANGER MESOMELIC DYSPLASIA | SHORT STATURE HOMEOBOX; SHOX
 
LCL
 
B-Lymphocyte
 
 
 
 
LANGER MESOMELIC DYSPLASIA | SHORT STATURE HOMEOBOX; SHOX
 
LCL
 
B-Lymphocyte
 
 
 
 
LANGER MESOMELIC DYSPLASIA | SHORT STATURE HOMEOBOX; SHOX
 
LCL
 
B-Lymphocyte
 
 
 
 
LANGER MESOMELIC DYSPLASIA | SHORT STATURE HOMEOBOX; SHOX
 
LCL
 
B-Lymphocyte
 
 
 
 
MYOPATHY, CENTRONUCLEAR, 1; CNM1 | MYOPATHY, PROXIMAL, WITH EARLY RESPIRATORY MUSCLE INVOLVEMENT; MPRM | TITIN; TTN | GAP JUNCTION PROTEIN, BETA-2; GJB2 (CONNEXIN 26; CX26)
 
LCL
 
B-Lymphocyte
 
 
 
 
MYOPATHY, CENTRONUCLEAR, 1; CNM1 | MYOPATHY, PROXIMAL, WITH EARLY RESPIRATORY MUSCLE INVOLVEMENT; MPRM | TITIN; TTN | GAP JUNCTION PROTEIN, BETA-2; GJB2 (CONNEXIN 26; CX26)
 
DNA
 
LCL
 
 
 
 
MYOPATHY, CENTRONUCLEAR, 1; CNM1 | MYOPATHY, PROXIMAL, WITH EARLY RESPIRATORY MUSCLE INVOLVEMENT; MPRM | TITIN; TTN | GAP JUNCTION PROTEIN, BETA-2; GJB2 (CONNEXIN 26; CX26)
 
High Molecular Weight DNA
 
B-Lymphocyte
 
 
 
 
MYOPATHY, CENTRONUCLEAR, 1; CNM1 | MYOPATHY, PROXIMAL, WITH EARLY RESPIRATORY MUSCLE INVOLVEMENT; MPRM | TITIN; TTN | GAP JUNCTION PROTEIN, BETA-2; GJB2 (CONNEXIN 26; CX26)
 
Fibroblast
 
Skin, Arm

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