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On page 1 showing 1 ~ 20 out of 1,669 results
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  • RRID:CVCL_X222

https://web.expasy.org/cellosaurus/CVCL_X222

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: African American.

Proper citation: Coriell Cat# GM00017, RRID:CVCL_X222 Copy   


  • RRID:CVCL_7267

https://web.expasy.org/cellosaurus/CVCL_7267

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: African American.

Proper citation: RRID:CVCL_7267 Copy   


  • RRID:CVCL_X224

https://web.expasy.org/cellosaurus/CVCL_X224

Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,X,i(X)(p11.21) (PubMed=10377420)., Population: Caucasian.

Proper citation: Coriell Cat# GM00088, RRID:CVCL_X224 Copy   


  • RRID:CVCL_V746

https://web.expasy.org/cellosaurus/CVCL_V746

Organism: Homo sapiens (Human)
Disease: Wolf-Hirschhorn syndrome
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM00072, RRID:CVCL_V746 Copy   


  • RRID:CVCL_H959

https://web.expasy.org/cellosaurus/CVCL_H959

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

Proper citation: RRID:CVCL_H959 Copy   


  • RRID:CVCL_X225

https://web.expasy.org/cellosaurus/CVCL_X225

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

Proper citation: Coriell Cat# GM00137, RRID:CVCL_X225 Copy   


  • RRID:CVCL_H959

https://web.expasy.org/cellosaurus/CVCL_H959

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

Proper citation: Coriell Cat# GM00090, RRID:CVCL_H959 Copy   


  • RRID:CVCL_X224

https://web.expasy.org/cellosaurus/CVCL_X224

Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,X,i(X)(p11.21) (PubMed=10377420)., Population: Caucasian.

Proper citation: RRID:CVCL_X224 Copy   


  • RRID:CVCL_V756

https://web.expasy.org/cellosaurus/CVCL_V756

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

Proper citation: Coriell Cat# GM00214, RRID:CVCL_V756 Copy   


  • RRID:CVCL_V753

https://web.expasy.org/cellosaurus/CVCL_V753

Organism: Homo sapiens (Human)
Disease: 49,XXXXY syndrome
Category: Finite cell line
Comments: Karyotypic information: 49,XXXXY,t(4;11)(q35;q23).arr(X)x4,(Y)x1 (Coriell=GM00157)., Population: Caucasian.

Proper citation: RRID:CVCL_V753 Copy   


  • RRID:CVCL_V756

https://web.expasy.org/cellosaurus/CVCL_V756

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

Proper citation: RRID:CVCL_V756 Copy   


  • RRID:CVCL_V766

https://web.expasy.org/cellosaurus/CVCL_V766

Organism: Homo sapiens (Human)
Disease: Wolf-Hirschhorn syndrome
Category: Finite cell line
Comments:

Proper citation: Coriell Cat# GM00343, RRID:CVCL_V766 Copy   


  • RRID:CVCL_V766

https://web.expasy.org/cellosaurus/CVCL_V766

Organism: Homo sapiens (Human)
Disease: Wolf-Hirschhorn syndrome
Category: Finite cell line
Comments:

Proper citation: RRID:CVCL_V766 Copy   


  • RRID:CVCL_V774

https://web.expasy.org/cellosaurus/CVCL_V774

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

Proper citation: Coriell Cat# GM00501, RRID:CVCL_V774 Copy   


  • RRID:CVCL_0P86

https://web.expasy.org/cellosaurus/CVCL_0P86

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,X,t(X;9)(q13.1;p24) (PubMed=10377420)., Population: Caucasian.

Proper citation: RRID:CVCL_0P86 Copy   


  • RRID:CVCL_0P86

https://web.expasy.org/cellosaurus/CVCL_0P86

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,X,t(X;9)(q13.1;p24) (PubMed=10377420)., Population: Caucasian.

Proper citation: Coriell Cat# GM00705, RRID:CVCL_0P86 Copy   


  • RRID:CVCL_X235

https://web.expasy.org/cellosaurus/CVCL_X235

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

Proper citation: Coriell Cat# GM00692, RRID:CVCL_X235 Copy   


  • RRID:CVCL_X076

https://web.expasy.org/cellosaurus/CVCL_X076

Organism: Homo sapiens (Human)
Disease: Isodicentric chromosome
Category: Finite cell line
Comments: Karyotypic information: 46,X,i(X)(p11) (PubMed=10377420)., Population: Caucasian.

Proper citation: RRID:CVCL_X076 Copy   


  • RRID:CVCL_4E27

https://web.expasy.org/cellosaurus/CVCL_4E27

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

Proper citation: Coriell Cat# GM00782, RRID:CVCL_4E27 Copy   


  • RRID:CVCL_V784

https://web.expasy.org/cellosaurus/CVCL_V784

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

Proper citation: RRID:CVCL_V784 Copy   



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