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Cell
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September 28, 2000
Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the Hyper-IgM syndrome (HIGM2)
P Revy, T Muto, Y Levy, et al.
Journal of Medical Genetics
|
September 26, 2007
Clinical spectrum of immunodeficiency, centromeric instability and facial dysmorphism (ICF syndrome)
M M Hagleitner, A Lankester, P Maraschio, et al.
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of 3
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Showing results (21-30 of 22) with videos related to
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This site can display upto 22 results.
Cell
|
September 28, 2000
Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the Hyper-IgM syndrome (HIGM2)
P Revy, T Muto, Y Levy, et al.
Journal of Medical Genetics
|
September 26, 2007
Clinical spectrum of immunodeficiency, centromeric instability and facial dysmorphism (ICF syndrome)
M M Hagleitner, A Lankester, P Maraschio, et al.
Page
of 3