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On page 205 showing 4081 ~ 4100 out of 20,547 results
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  • RRID:CVCL_AZ55

https://web.expasy.org/cellosaurus/CVCL_AZ55

Organism: Homo sapiens (Human)
Disease: Rigid spine muscular dystrophy 1
Category: Finite cell line

Proper citation: RRID:CVCL_AZ55 Copy   


  • RRID:CVCL_AZ54

https://web.expasy.org/cellosaurus/CVCL_AZ54

Organism: Homo sapiens (Human)
Disease: Bethlem myopathy 1
Category: Finite cell line

Proper citation: RRID:CVCL_AZ54 Copy   


  • RRID:CVCL_AZ54

https://web.expasy.org/cellosaurus/CVCL_AZ54

Organism: Homo sapiens (Human)
Disease: Bethlem myopathy 1
Category: Finite cell line

Proper citation: Coriell Cat# GM24406, RRID:CVCL_AZ54 Copy   


  • RRID:CVCL_AZ28

https://web.expasy.org/cellosaurus/CVCL_AZ28

Organism: Homo sapiens (Human)
Disease: Anencephaly
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_AZ28 Copy   


  • RRID:CVCL_AZ39

https://web.expasy.org/cellosaurus/CVCL_AZ39

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Jewish; Ashkenazi.

Proper citation: RRID:CVCL_AZ39 Copy   


  • RRID:CVCL_5T42

https://web.expasy.org/cellosaurus/CVCL_5T42

Organism: Homo sapiens (Human)
Category: Finite cell line

Proper citation: RRID:CVCL_5T42 Copy   


  • RRID:CVCL_AZ53

https://web.expasy.org/cellosaurus/CVCL_AZ53

Organism: Homo sapiens (Human)
Disease: Congenital muscular dystrophy-dystroglycanopathy with intellectual developmental disorder type B2
Category: Finite cell line
Comments: Population: Caucasian; German/Irish.

Proper citation: RRID:CVCL_AZ53 Copy   


  • RRID:CVCL_4T71

https://web.expasy.org/cellosaurus/CVCL_4T71

Organism: Homo sapiens (Human)
Disease: Ullrich congenital muscular dystrophy
Category: Finite cell line

Proper citation: RRID:CVCL_4T71 Copy   


  • RRID:CVCL_5T41

https://web.expasy.org/cellosaurus/CVCL_5T41

Organism: Homo sapiens (Human)
Category: Finite cell line

Proper citation: Coriell Cat# GM24586, RRID:CVCL_5T41 Copy   


  • RRID:CVCL_JF29

https://web.expasy.org/cellosaurus/CVCL_JF29

Organism: Homo sapiens (Human)
Disease: Galloway-Mowat syndrome
Category: Finite cell line

Proper citation: RRID:CVCL_JF29 Copy   


  • RRID:CVCL_CX84

https://web.expasy.org/cellosaurus/CVCL_CX84

Organism: Homo sapiens (Human)
Category: Finite cell line

Proper citation: RRID:CVCL_CX84 Copy   


  • RRID:CVCL_BW54

https://web.expasy.org/cellosaurus/CVCL_BW54

Organism: Homo sapiens (Human)
Disease: Choroideremia
Category: Finite cell line

Proper citation: RRID:CVCL_BW54 Copy   


  • RRID:CVCL_5K72

https://web.expasy.org/cellosaurus/CVCL_5K72

Organism: Homo sapiens (Human)
Disease: Smith-Magenis syndrome
Category: Finite cell line

Proper citation: Coriell Cat# GM25350, RRID:CVCL_5K72 Copy   


  • RRID:CVCL_HQ18

https://web.expasy.org/cellosaurus/CVCL_HQ18

Organism: Homo sapiens (Human)
Disease: Nemaline myopathy 3
Category: Finite cell line

Proper citation: RRID:CVCL_HQ18 Copy   


  • RRID:CVCL_BA19

https://web.expasy.org/cellosaurus/CVCL_BA19

Organism: Homo sapiens (Human)
Disease: Smith-Magenis syndrome
Category: Finite cell line

Proper citation: RRID:CVCL_BA19 Copy   


  • RRID:CVCL_BW52

https://web.expasy.org/cellosaurus/CVCL_BW52

Organism: Homo sapiens (Human)
Disease: Choroideremia
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_BW52 Copy   


  • RRID:CVCL_5K89

https://web.expasy.org/cellosaurus/CVCL_5K89

Organism: Homo sapiens (Human)
Disease: Smith-Magenis syndrome
Category: Finite cell line

Proper citation: Coriell Cat# GM25374, RRID:CVCL_5K89 Copy   


  • RRID:CVCL_5K92

https://web.expasy.org/cellosaurus/CVCL_5K92

Organism: Homo sapiens (Human)
Disease: Smith-Magenis syndrome
Category: Finite cell line

Proper citation: Coriell Cat# GM25378, RRID:CVCL_5K92 Copy   


  • RRID:CVCL_5K84

https://web.expasy.org/cellosaurus/CVCL_5K84

Organism: Homo sapiens (Human)
Disease: Smith-Magenis syndrome
Category: Finite cell line

Proper citation: Coriell Cat# GM25367, RRID:CVCL_5K84 Copy   


  • RRID:CVCL_5K87

https://web.expasy.org/cellosaurus/CVCL_5K87

Organism: Homo sapiens (Human)
Disease: Smith-Magenis syndrome
Category: Finite cell line

Proper citation: Coriell Cat# GM25372, RRID:CVCL_5K87 Copy   



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