| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/AJMG.A.33445 |
| P698 | PubMed publication ID | 20803646 |
| P50 | author | Shirley Hodgson | Q15995134 |
| Pia Ostergaard | Q41928183 | ||
| Colin Steward | Q42685096 | ||
| P2093 | author name string | Inderjeet Dokal | |
| Tom Vulliamy | |||
| Victoria Murday | |||
| Sarah Smithson | |||
| Ghulam Mufti | |||
| Brenda Gibson | |||
| Glen Brice | |||
| Kamini Kalidas | |||
| Sahar Mansour | |||
| Steve Jeffery | |||
| Peter Lunt | |||
| Lorna Tinworth | |||
| Peter Mortimer | |||
| Fiona Connell | |||
| Russell Keenan | |||
| Jackie Cornish | |||
| Sally Cottrell | |||
| Louise Kiely | |||
| P433 | issue | 9 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 2287-2296 | |
| P577 | publication date | 2010-08-20 | |
| P1433 | published in | American Journal of Medical Genetics | Q4744254 |
| P1476 | title | Emberger syndrome-Primary lymphedema with myelodysplasia: Report of seven new cases | |
| P478 | volume | 152A |
| Q48504653 | Allogeneic Hematopoietic Stem-Cell Transplantation for GATA2 Deficiency Using a Busulfan-Based Regimen. |
| Q55514852 | Bacille Calmette–Guerin Complications in Newly Described Primary Immunodeficiency Diseases: 2010–2017. |
| Q38180646 | Cancer genomics and inherited risk |
| Q52597254 | Differential effects on gene transcription and hematopoietic differentiation correlate with GATA2 mutant disease phenotypes. |
| Q43089162 | First Korean case of Emberger syndrome (primary lymphedema with myelodysplasia) with a novel GATA2 gene mutation |
| Q50027819 | GATA-2 anomaly and clinical phenotype of a sporadic case of lymphedema, dendritic cell, monocyte, B- and NK-cell (DCML) deficiency, and myelodysplasia |
| Q40163308 | GATA2 deficiency and related myeloid neoplasms |
| Q37564756 | GATA2 deficiency: a protean disorder of hematopoiesis, lymphatics, and immunity. |
| Q36040456 | GATA2 is required for lymphatic vessel valve development and maintenance. |
| Q85009395 | GATA2 mutations lead to MDS and AML |
| Q40303868 | GATA2 null mutation associated with incomplete penetrance in a family with Emberger syndrome. |
| Q33428604 | Genetic predisposition to myelodysplastic syndrome and acute myeloid leukemia in children and young adults |
| Q40641835 | Haploidentical hematopoietic stem cell transplantation in children with high-risk hematologic malignancies: outcomes with two different strategies for GvHD prevention. Ex vivo T-cell depletion and post-transplant cyclophosphamide: 10 years of experi |
| Q47649061 | Hdac3 regulates lymphovenous and lymphatic valve formation. |
| Q26828941 | Heritable GATA2 mutations associated with familial AML-MDS: a case report and review of literature |
| Q35249294 | Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia |
| Q37023060 | High frequency of GATA2 mutations in patients with mild chronic neutropenia evolving to MonoMac syndrome, myelodysplasia, and acute myeloid leukemia. |
| Q38518485 | Host susceptibility to non-tuberculous mycobacterial infections |
| Q35510477 | Inherited and acquired immunodeficiencies underlying tuberculosis in childhood |
| Q35750366 | Loss-of-function germline GATA2 mutations in patients with MDS/AML or MonoMAC syndrome and primary lymphedema reveal a key role for GATA2 in the lymphatic vasculature |
| Q26782052 | Master regulatory GATA transcription factors: mechanistic principles and emerging links to hematologic malignancies |
| Q37674302 | Mechanism governing a stem cell-generating cis-regulatory element |
| Q45829967 | MonoMAC and GATA2 deficiency: overlapping clinical and pathological features with aplastic anemia and idiopathic CD4+ lymphocytopenia. Reply to Haematologica 2012;97(4):058669. |
| Q55671562 | Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome) |
| Q34619834 | Nonmyeloablative allogeneic hematopoietic stem cell transplantation for GATA2 deficiency |
| Q51022410 | Severe disseminated primary herpes simplex infection as skin manifestation of GATA2 deficiency. |
| Q38896796 | Successful umbilical cord blood hematopoietic stem cell transplantation in pediatric patients with MDS/AML associated with underlying GATA2 mutations: two case reports and review of literature |
| Q38102064 | The classification and diagnostic algorithm for primary lymphatic dysplasia: an update from 2010 to include molecular findings. |
| Q37564769 | The evolution of cellular deficiency in GATA2 mutation |
| Q33848134 | The role of GATA2 in lethal prostate cancer aggressiveness |
| Q36455030 | Warts and all: human papillomavirus in primary immunodeficiencies |
Search more.