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On page 97 showing 1921 ~ 1940 out of 20,547 results
Snippet view Table view Download Top 1000 Results
Click the to add this resource to an Authentication Report or Collection
  • RRID:CVCL_GS68

https://web.expasy.org/cellosaurus/CVCL_GS68

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

Proper citation: RRID:CVCL_GS68 Copy   


  • RRID:CVCL_X314

https://web.expasy.org/cellosaurus/CVCL_X314

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

Proper citation: RRID:CVCL_X314 Copy   


  • RRID:CVCL_5N00

https://web.expasy.org/cellosaurus/CVCL_5N00

Organism: Homo sapiens (Human)
Disease: Dyggve-Melchior-Clausen syndrome
Category: Finite cell line
Comments: Population: Lebanese.

Proper citation: Coriell Cat# GM04997, RRID:CVCL_5N00 Copy   


  • RRID:CVCL_IJ36

https://web.expasy.org/cellosaurus/CVCL_IJ36

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

Proper citation: Coriell Cat# GM05076, RRID:CVCL_IJ36 Copy   


  • RRID:CVCL_AB35

https://web.expasy.org/cellosaurus/CVCL_AB35

Organism: Homo sapiens (Human)
Disease: Triploidy syndrome
Category: Finite cell line
Comments: Karyotypic information: 69,XXX (Coriell=GM04939)., Population: Caucasian.

Proper citation: Coriell Cat# GM04939, RRID:CVCL_AB35 Copy   


  • RRID:CVCL_V479

https://web.expasy.org/cellosaurus/CVCL_V479

Organism: Homo sapiens (Human)
Disease: Down syndrome
Category: Finite cell line
Comments: Population: Asian.

Proper citation: RRID:CVCL_V479 Copy   


  • RRID:CVCL_5N29

https://web.expasy.org/cellosaurus/CVCL_5N29

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

Proper citation: Coriell Cat# GM05173, RRID:CVCL_5N29 Copy   


  • RRID:CVCL_DS13

https://web.expasy.org/cellosaurus/CVCL_DS13

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

Proper citation: Coriell Cat# GM05091, RRID:CVCL_DS13 Copy   


  • RRID:CVCL_5N16

https://web.expasy.org/cellosaurus/CVCL_5N16

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

Proper citation: RRID:CVCL_5N16 Copy   


  • RRID:CVCL_AW57

https://web.expasy.org/cellosaurus/CVCL_AW57

Organism: Homo sapiens (Human)
Disease: Dystrophia myotonica 1
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM05142, RRID:CVCL_AW57 Copy   


  • RRID:CVCL_5N08

https://web.expasy.org/cellosaurus/CVCL_5N08

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

Proper citation: RRID:CVCL_5N08 Copy   


  • RRID:CVCL_AX80

https://web.expasy.org/cellosaurus/CVCL_AX80

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

Proper citation: RRID:CVCL_AX80 Copy   


  • RRID:CVCL_DD78

https://web.expasy.org/cellosaurus/CVCL_DD78

Organism: Homo sapiens (Human)
Disease: Osteogenesis imperfecta type I
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM05181, RRID:CVCL_DD78 Copy   


  • RRID:CVCL_DS13

https://web.expasy.org/cellosaurus/CVCL_DS13

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

Proper citation: RRID:CVCL_DS13 Copy   


  • RRID:CVCL_X317

https://web.expasy.org/cellosaurus/CVCL_X317

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,XY,der(14)(14qter->14p11.2::20p11.1->20pter)mat (Coriell=GM05133)., Population: African American.

Proper citation: Coriell Cat# GM05133, RRID:CVCL_X317 Copy   


  • RRID:CVCL_1K28

https://web.expasy.org/cellosaurus/CVCL_1K28

Organism: Homo sapiens (Human)
Disease: Charcot-Marie-Tooth disease type 1A
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM05167, RRID:CVCL_1K28 Copy   


  • RRID:CVCL_AW62

https://web.expasy.org/cellosaurus/CVCL_AW62

Organism: Homo sapiens (Human)
Disease: Dystrophia myotonica 1
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM05208, RRID:CVCL_AW62 Copy   


  • RRID:CVCL_1K28

https://web.expasy.org/cellosaurus/CVCL_1K28

Organism: Homo sapiens (Human)
Disease: Charcot-Marie-Tooth disease type 1A
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_1K28 Copy   


  • RRID:CVCL_1Q24

https://web.expasy.org/cellosaurus/CVCL_1Q24

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,XY,t(6;7)(q21;q21.2) (Coriell=GM05183)., Population: Caucasian; Italian.

Proper citation: RRID:CVCL_1Q24 Copy   


  • RRID:CVCL_5N18

https://web.expasy.org/cellosaurus/CVCL_5N18

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

Proper citation: RRID:CVCL_5N18 Copy   



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