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On page 92 showing 1821 ~ 1840 out of 20,547 results
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  • RRID:CVCL_9N93

https://web.expasy.org/cellosaurus/CVCL_9N93

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XY,t(4;12)(q32.2;21.2)mat (ECACC=98082509)., Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 98082509, RRID:CVCL_9N93 Copy   


  • RRID:CVCL_9N97

https://web.expasy.org/cellosaurus/CVCL_9N97

Organism: Homo sapiens (Human)
Disease: Aortic valve stenosis
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.

Proper citation: RRID:CVCL_9N97 Copy   


  • RRID:CVCL_9N93

https://web.expasy.org/cellosaurus/CVCL_9N93

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XY,t(4;12)(q32.2;21.2)mat (ECACC=98082509)., Part of: ECACC chromosomal abnormality collection.

Proper citation: RRID:CVCL_9N93 Copy   


  • RRID:CVCL_9P03

https://web.expasy.org/cellosaurus/CVCL_9P03

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(1;4)(q23;p15.3)mat (ECACC=98102201)., Part of: ECACC chromosomal abnormality collection.

Proper citation: RRID:CVCL_9P03 Copy   


  • RRID:CVCL_9P03

https://web.expasy.org/cellosaurus/CVCL_9P03

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(1;4)(q23;p15.3)mat (ECACC=98102201)., Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 98102201, RRID:CVCL_9P03 Copy   


  • RRID:CVCL_9N89

https://web.expasy.org/cellosaurus/CVCL_9N89

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.

Proper citation: RRID:CVCL_9N89 Copy   


  • RRID:CVCL_9P04

https://web.expasy.org/cellosaurus/CVCL_9P04

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XY,der(11)t(3;11)(q27.3;q24.2)pat (ECACC=98102202)., Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 98102202, RRID:CVCL_9P04 Copy   


  • RRID:CVCL_9N83

https://web.expasy.org/cellosaurus/CVCL_9N83

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 98072204, RRID:CVCL_9N83 Copy   


  • RRID:CVCL_9M70

https://web.expasy.org/cellosaurus/CVCL_9M70

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.

Proper citation: RRID:CVCL_9M70 Copy   


  • RRID:CVCL_9M85

https://web.expasy.org/cellosaurus/CVCL_9M85

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,del(17)(qter->p13.3).ish del(17) (ECACC=98110617)., Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 98110617, RRID:CVCL_9M85 Copy   


  • RRID:CVCL_9M87

https://web.expasy.org/cellosaurus/CVCL_9M87

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,inv(17)(p?11;q?12) (ECACC=98111707)., Part of: ECACC chromosomal abnormality collection.

Proper citation: RRID:CVCL_9M87 Copy   


  • RRID:CVCL_9P36

https://web.expasy.org/cellosaurus/CVCL_9P36

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 98121013, RRID:CVCL_9P36 Copy   


  • RRID:CVCL_IJ35

https://web.expasy.org/cellosaurus/CVCL_IJ35

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

Proper citation: Coriell Cat# GM02438, RRID:CVCL_IJ35 Copy   


  • RRID:CVCL_JD75

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_JD75

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

Proper citation: Coriell Cat# GM02364, RRID:CVCL_JD75 Copy   


  • RRID:CVCL_CZ14

https://web.expasy.org/cellosaurus/CVCL_CZ14

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

Proper citation: RRID:CVCL_CZ14 Copy   


  • RRID:CVCL_D869

https://web.expasy.org/cellosaurus/CVCL_D869

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

Proper citation: Coriell Cat# GM02338, RRID:CVCL_D869 Copy   


  • RRID:CVCL_X263

https://web.expasy.org/cellosaurus/CVCL_X263

Organism: Homo sapiens (Human)
Disease: Trisomy 9
Category: Finite cell line
Comments: Karyotypic information: 47,XX,+9 [5]; 46,XX [45] (Coriell=GM02329)., Population: Caucasian.

Proper citation: Coriell Cat# GM02329, RRID:CVCL_X263 Copy   


  • RRID:CVCL_AK22

https://web.expasy.org/cellosaurus/CVCL_AK22

Organism: Homo sapiens (Human)
Disease: Fanconi anemia, complementation group G
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_AK22 Copy   


  • RRID:CVCL_GR98

https://web.expasy.org/cellosaurus/CVCL_GR98

Organism: Homo sapiens (Human)
Disease: Type 1 diabetes mellitus
Category: Finite cell line
Comments: Population: Native Central American; Pima.

Proper citation: RRID:CVCL_GR98 Copy   


  • RRID:CVCL_AA18

https://web.expasy.org/cellosaurus/CVCL_AA18

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

Proper citation: RRID:CVCL_AA18 Copy   



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