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[HTML][HTML] Spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis

KG Ericson, B Fadeel, S Nilsson-Ardnor… - The American Journal of …, 2001 - cell.com
Familial hemophagocytic lymphohistiocytosis (FHL) is an autosomal recessive disease of
early childhood characterized by nonmalignant accumulation and multivisceral infiltration of …
被引用次数：333 相关文章
[HTML] nih.gov

[HTML][HTML] Spectrum of Perforin Gene Mutations in Familial Hemophagocytic Lymphohistiocytosis

KG Ericson, B Fadeel, S Nilsson-Ardnor… - American Journal of …, 2001 - ncbi.nlm.nih.gov
Familial hemophagocytic lymphohistiocytosis (FHL) is an autosomal recessive disease of
early childhood characterized by nonmalignant accumulation and multivisceral infiltration of …

Spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis

KG Ericson, B Fadeel… - … journal of human …, 2001 - pubmed.ncbi.nlm.nih.gov
Familial hemophagocytic lymphohistiocytosis (FHL) is an autosomal recessive disease of
early childhood characterized by nonmalignant accumulation and multivisceral infiltration of …

Spectrum of Perforin Gene Mutations in Familial Hemophagocytic Lymphohistiocytosis

KG Ericson, B Fadeel, S Nilsson-Ardnor… - The American Journal of …, 2001 - infona.pl
Familial hemophagocytic lymphohistiocytosis (FHL) is an autosomal recessive disease of
early childhood characterized by nonmalignant accumulation and multivisceral infiltration of …
[PDF] academia.edu

[PDF][PDF] Spectrum of Perforin Gene Mutations in Familial Hemophagocytic Lymphohistiocytosis

KG Ericson, B Fadeel, S Nilsson-Ardnor… - Am. J. Hum …, 2001 - academia.edu
Familial hemophagocytic lymphohistiocytosis (FHL) is an autosomal recessive disease of
early childhood characterized by nonmalignant accumulation and multivisceral infiltration of …
[PDF] core.ac.uk

[PDF][PDF] Spectrum of Perforin Gene Mutations in Familial Hemophagocytic Lymphohistiocytosis

KG Ericson, B Fadeel, S Nilsson-Ardnor… - Am. J. Hum …, 2001 - core.ac.uk
Familial hemophagocytic lymphohistiocytosis (FHL) is an autosomal recessive disease of
early childhood characterized by nonmalignant accumulation and multivisceral infiltration of …
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[HTML][HTML] Spectrum of Perforin Gene Mutations in Familial Hemophagocytic Lymphohistiocytosis

KG Ericson, B Fadeel, S Nilsson-Ardnor… - The American Journal of …, 2001 - Elsevier
Familial hemophagocytic lymphohistiocytosis (FHL) is an autosomal recessive disease of
early childhood characterized by nonmalignant accumulation and multivisceral infiltration of …

[引用][C] Spectrum of Perforin Gene Mutations in Familial Hemophagocytic Lymphohistiocytosis

KG Ericson, B Fadeel, S Nilsson-Ardnor… - The American Journal …, 2001 - cir.nii.ac.jp
Spectrum of Perforin Gene Mutations in Familial Hemophagocytic Lymphohistiocytosis |
CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] 詳細へ移動 検索フォーム …

Spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis.

B Fadeel, S Nilsson-Ardnor, C Söderhäll… - American Journal of …, 2001 - europepmc.org
Familial hemophagocytic lymphohistiocytosis (FHL) is an autosomal recessive disease of
early childhood characterized by nonmalignant accumulation and multivisceral infiltration of …

Spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis

KG Ericson, B Fadeel, S Nilsson-Ardnor… - AMERICAN …, 2001 - avesis.istanbul.edu.tr
Familial hemophagocytic lymphohistiocytosis (FHL) is an autosomal recessive disease of
early childhood characterized by nonmalignant accumulation and multivisceral infiltration of …