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On page 83 showing 1641 ~ 1660 out of 117,735 results
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  • RRID:CVCL_GY28

https://web.expasy.org/cellosaurus/CVCL_GY28

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

Proper citation: Coriell Cat# GM11328, RRID:CVCL_GY28 Copy   


  • RRID:CVCL_V231

https://web.expasy.org/cellosaurus/CVCL_V231

Organism: Homo sapiens (Human)
Disease: Cystic fibrosis
Category: Transformed cell line
Comments: Part of: Genetic Testing Reference Material (GeT-RM) samples.

Proper citation: RRID:CVCL_V231 Copy   


  • RRID:CVCL_4F32

https://web.expasy.org/cellosaurus/CVCL_4F32

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

Proper citation: Coriell Cat# GM11315, RRID:CVCL_4F32 Copy   


  • RRID:CVCL_N171

https://web.expasy.org/cellosaurus/CVCL_N171

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Chinese., Part of: Yale-Stanford Collection from NIGMS Human Genetic Cell Repository., Part of: Human variation panel.

Proper citation: Coriell Cat# GM11322, RRID:CVCL_N171 Copy   


  • RRID:CVCL_U883

https://web.expasy.org/cellosaurus/CVCL_U883

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

Proper citation: RRID:CVCL_U883 Copy   


  • RRID:CVCL_AM56

https://web.expasy.org/cellosaurus/CVCL_AM56

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

Proper citation: RRID:CVCL_AM56 Copy   


  • RRID:CVCL_2U03

https://web.expasy.org/cellosaurus/CVCL_2U03

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XY,t(7;17)(7pter->7p10::17p13.3->17pter;17qter->17p13.3::7q10->7qter) (Coriell=GM11251)., Population: Caucasian.

Proper citation: RRID:CVCL_2U03 Copy   


  • RRID:CVCL_4F29

https://web.expasy.org/cellosaurus/CVCL_4F29

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

Proper citation: Coriell Cat# GM11312, RRID:CVCL_4F29 Copy   


  • RRID:CVCL_N170

https://web.expasy.org/cellosaurus/CVCL_N170

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Chinese., Part of: Yale-Stanford Collection from NIGMS Human Genetic Cell Repository., Part of: Human variation panel.

Proper citation: RRID:CVCL_N170 Copy   


  • RRID:CVCL_N174

https://web.expasy.org/cellosaurus/CVCL_N174

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Chinese., Part of: Yale-Stanford Collection from NIGMS Human Genetic Cell Repository., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples.

Proper citation: RRID:CVCL_N174 Copy   


  • RRID:CVCL_U882

https://web.expasy.org/cellosaurus/CVCL_U882

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

Proper citation: RRID:CVCL_U882 Copy   


  • RRID:CVCL_V221

https://web.expasy.org/cellosaurus/CVCL_V221

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

Proper citation: RRID:CVCL_V221 Copy   


  • RRID:CVCL_GY28

https://web.expasy.org/cellosaurus/CVCL_GY28

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

Proper citation: RRID:CVCL_GY28 Copy   


  • RRID:CVCL_2U06

https://web.expasy.org/cellosaurus/CVCL_2U06

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 45,XY,der(14)(14qter->14p12::18q11->18qter),-18 (Coriell=GM11346)., Population: Caucasian.

Proper citation: RRID:CVCL_2U06 Copy   


  • RRID:CVCL_AJ48

https://web.expasy.org/cellosaurus/CVCL_AJ48

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian., Part of: R-W pedigree MODY cell line collection.

Proper citation: Coriell Cat# GM11333, RRID:CVCL_AJ48 Copy   


  • RRID:CVCL_5P52

https://web.expasy.org/cellosaurus/CVCL_5P52

Organism: Homo sapiens (Human)
Disease: Angelman syndrome
Category: Transformed cell line
Comments:

Proper citation: Coriell Cat# GM11404, RRID:CVCL_5P52 Copy   


  • RRID:CVCL_N179

https://web.expasy.org/cellosaurus/CVCL_N179

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Jewish; Ashkenazi., Part of: Human variation panel.

Proper citation: RRID:CVCL_N179 Copy   


  • RRID:CVCL_5P46

https://web.expasy.org/cellosaurus/CVCL_5P46

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

Proper citation: Coriell Cat# GM11387, RRID:CVCL_5P46 Copy   


  • RRID:CVCL_GS78

https://web.expasy.org/cellosaurus/CVCL_GS78

Organism: Homo sapiens (Human)
Disease: Adenosine deaminase deficiency
Category: Transformed cell line
Comments: Population: Caucasian; Amish.

Proper citation: RRID:CVCL_GS78 Copy   


  • RRID:CVCL_U532

https://web.expasy.org/cellosaurus/CVCL_U532

Organism: Homo sapiens (Human)
Disease: Prader-Willi syndrome
Category: Transformed cell line
Comments:

Proper citation: RRID:CVCL_U532 Copy   



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