Homo sapiens lymphocyte-predominant Hodgkin's disease case #4 immunogl - Nucleotide

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Analysis of somatic hypermutation in X-linked hyper-IgM syndrome shows specific deficiencies in mutational targeting. [Blood. 2009]
Analysis of somatic hypermutation in X-linked hyper-IgM syndrome shows specific deficiencies in mutational targeting.
Longo NS, Lugar PL, Yavuz S, Zhang W, Krijger PH, Russ DE, Jima DD, Dave SS, Grammer AC, Lipsky PE. Blood. 2009 Apr 16; 113(16):3706-15. Epub 2008 Nov 20.
Origin of nodular lymphocyte-predominant Hodgkin's disease from a clonal expansion of highly mutated germinal-center B cells. [N Engl J Med. 1997]
Origin of nodular lymphocyte-predominant Hodgkin's disease from a clonal expansion of highly mutated germinal-center B cells.
Marafioti T, Hummel M, Anagnostopoulos I, Foss HD, Falini B, Delsol G, Isaacson PG, Pileri S, Stein H. N Engl J Med. 1997 Aug 14; 337(7):453-8.
The repertoire of human germline VH sequences reveals about fifty groups of VH segments with different hypervariable loops. [J Mol Biol. 1992]
The repertoire of human germline VH sequences reveals about fifty groups of VH segments with different hypervariable loops.
Tomlinson IM, Walter G, Marks JD, Llewelyn MB, Winter G. J Mol Biol. 1992 Oct 5; 227(3):776-98.

IMGT, the international ImMunoGeneTics information system [IMGT, the international ImMun...]
IMGT, the international ImMunoGeneTics information system

Homo sapiens lymphocyte-predominant Hodgkin's disease case #4 immunoglobulin hea...
Homo sapiens lymphocyte-predominant Hodgkin's disease case #4 immunoglobulin heavy chain gene, variable region, partial cds
gi|2852420|gb|AF044592.1|

Nucleotide
ClinVar for MedGen (Select 78665) (182)
ClinVar
Osteogenesis imperfecta type 6
Osteogenesis imperfecta type 6

MedGen
Osteogenesis imperfecta type 14
Osteogenesis imperfecta type 14

MedGen

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Nucleotide