TY  - GEN
AU  - Ishida,Hiroyuki
AU  - Imai,Kosuke
AU  - Honma,Kenichi
AU  - Tamura,Shin-Ichi
AU  - Imamura,Toshihiko
AU  - Ito,Masafumi
AU  - Nonoyama,Shigeaki
TI  - GATA-2 anomaly and clinical phenotype of a sporadic case of lymphedema, dendritic cell, monocyte, B- and NK-cell (DCML) deficiency, and myelodysplasia
SN  - 1432-1076
PY  - 2012///1204
KW  - Female
KW  - GATA2 Transcription Factor
KW  - genetics
KW  - Genetic Markers
KW  - Humans
KW  - Immunologic Deficiency Syndromes
KW  - diagnosis
KW  - Lymphedema
KW  - Mutation, Missense
KW  - Myelodysplastic Syndromes
KW  - Phenotype
KW  - Syndrome
KW  - Young Adult
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1007/s00431-012-1715-7
ER  -