Clear Filter
  • (1767)
  • (61)
  • (786)
  • (521)
  • (376)
  • (49)
  • (20)
  • (12)
  • (2)
  • (1)
  • (797)
  • (366)
  • (175)
  • (83)
  • (51)
  • (35)
  • (15)
  • (12)
  • (3)
  • (2)
  • (2)
  • (2)
  • (2)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1525)
  • (220)
  • (20)
  • (2)
  • (1010)
  • (748)
  • (4)
  • (1297)
  • (81)
  • (34)
  • (21)
  • (21)
  • (20)
  • (12)
  • (9)
  • (9)
  • (7)
  • (5)
  • (3)
  • (3)
  • (2)
  • (2)
  • (1)
  • (1)
  • (1)
  • (1204)
  • (344)
  • (11)
  • (8)
  • (1080)
  • (687)
  • (350)
  • (278)
  • (181)
  • (177)
  • (204)
  • (145)
  • (145)
  • (89)
  • (49)
  • (1352)
  • (595)
  • (335)
  • (285)
  • (223)
  • (217)
  • (97)
  • (93)
  • (86)
  • (10)
  • (6)
  • (5)
  • (4)
  • (4)
  • (2)
  • (2)
  • (2)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1765)
  • (2)
  • (1474)
  • (293)
  Clear Filter

Search Results for - FUKUYAMA CONGENITAL MUSCULAR DYSTROPHY

 Use filters to refine search | Additional fields available - click "Fields" button
Loading ...
1 - 50 of 1767 Results
Selected Items: 0
Page Size:
 
 
Quick View
 
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, PROGRESSIVE WITH CNS INVOLVEMENT & RECESSIVE INHERITANCE
 
Fibroblast
 
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
Fibroblast
 
Skin, Unspecified
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
Fibroblast
 
Skin, Unspecified
 
 
 
 
ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD1
 
LCL
 
B-Lymphocyte
 
 
 
 
SELENON-RELATED MYOPATHY; RIGID SPINE MUSCULAR DYSTROPHY 1; RSMD1
 
LCL
 
B-Lymphocyte
 
 
 
 
SELENON-RELATED MYOPATHY; RIGID SPINE MUSCULAR DYSTROPHY 1; RSMD1
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
Fibroblast
 
Skin, Skin
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A | LAMININ, ALPHA-2; LAMA2
 
Fibroblast
 
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD1
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
DNA
 
Fibroblast
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A | LAMININ, ALPHA-2; LAMA2
 
Fibroblast
 
Skin, Skin
 
 
 
 
ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD1
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
Fibroblast
 
Skin, Skin
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
Fibroblast
 
Skin, Skin
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
Fibroblast
 
Skin, Skin
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
DNA
 
LCL
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
Fibroblast
 
Skin, Skin
 
 
 
 
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
 
 
 
 
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)
 
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, 1; MDDGA1 (WALKER-WARBURG SYNDROME INCLUDED)
 
DNA
 
LCL
 
 
 
 
SELENON-RELATED MYOPATHY; RIGID SPINE MUSCULAR DYSTROPHY 1; RSMD1 | SELENOPROTEIN N, 1; SEPN1
 
LCL
 
B-Lymphocyte
 
 
 
 
SELENON-RELATED MYOPATHY; RIGID SPINE MUSCULAR DYSTROPHY 1; RSMD1
 
LCL
 
B-Lymphocyte
 
 
 
 
SELENON-RELATED MYOPATHY; RIGID SPINE MUSCULAR DYSTROPHY 1; RSMD1 | SELENOPROTEIN N, 1; SEPN1
 
LCL
 
B-Lymphocyte
 
 
 
 
ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD1 | COLLAGEN, TYPE VI, ALPHA-2; COL6A2
 
LCL
 
B-Lymphocyte
 
 
 
 
ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD1 | COLLAGEN, TYPE VI, ALPHA-2; COL6A2
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7
 
Fibroblast
 
Skin, Unspecified
 
 
 
 
ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD1 | COLLAGEN, TYPE II, ALPHA-1; COL2A1
 
LCL
 
B-Lymphocyte

No Results were Found

1 - 50 of 1767 Results
Selected Items: 0
Page Size:

CORIELL RESEARCH SERVICES



Apart from our online Catalog, Coriell also offers the greater scientific community a wide range of laboratory services. Our custom services include iPSC services, R&D services, assay development, custom lab services, genomic services, bioinformatic analysis, etc., to name a few. 


Learn More 
(Open in New Tab)
Footer

Our mission is to prevent and cure disease through biomedical research.

CONTACT US

CUSTOMER SERVICE
customerservice@coriell.org (800) 752-3805 ● (856) 757-4848
Subscribe to our newsletter here

Coriell Institute for Medical Research
403 Haddon Avenue Camden, NJ 08103, USA (856) 966-7377

Ⓒ 2025 Coriell Institute. All rights reserved.