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Sushree Sangita Sahoo

6 cilt bulundu.

Cilt sonuçları

CiltCharacterization of Genes Predisposing to Bone Marrow Failure in ChildrenSushree Sangita Sahoo

Characterization of Genes Predisposing to Bone Marrow Failure in Children

Sushree Sangita Sahoo · Yayınevi bilinmiyor

Sayfa sayısı yok · 2018

Kategori yok

CiltCorrigendum: Clinical and Molecular Heterogeneity of RTEL1 DeficiencyCarsten Speckmann, Sushree Sangita Sahoo, Marta Rizzi, Shinsuke Hirabayashi, Liliana Annette Rindle, Maximilian Seidl, Anne Rensing-Ehl, Ekkehart Lausch, Brigitte Strahm, Stephan Ehl, Charlotte Niemeyer, Marcin W. Wlodarski

Corrigendum: Clinical and Molecular Heterogeneity of RTEL1 Deficiency

Carsten Speckmann, Sushree Sangita Sahoo, Marta Rizzi, Shinsuke Hirabayashi, Liliana Annette Rindle, Maximilian Seidl, Anne Rensing-Ehl, Ekkehart Lausch, Brigitte Strahm, Stephan Ehl, Charlotte Niemeyer, Marcin W. Wlodarski · Yayınevi bilinmiyor

Sayfa sayısı yok · 2017

Kategori yok

CiltGermline Predisposition in Myeloid Neoplasms: Unique Genetic and Clinical Features of GATA2 Deficiency and SAMD9/SAMD9L SyndromesSushree Sangita Sahoo, Emilia J. Kozyra, Marcin W. Wlodarski

Germline Predisposition in Myeloid Neoplasms: Unique Genetic and Clinical Features of GATA2 Deficiency and SAMD9/SAMD9L Syndromes

Sushree Sangita Sahoo, Emilia J. Kozyra, Marcin W. Wlodarski · Yayınevi bilinmiyor

Sayfa sayısı yok · 2020

Kategori yok

CiltClinical and Molecular Heterogeneity of RTEL1 DeficiencyCarsten Speckmann, Sushree Sangita Sahoo, Marta Rizzi, Shinsuke Hirabayashi, Liliana Annette Rindle, Maximilian Seidl, Anne Rensing-Ehl, Ekkehart Lausch, Brigitte Strahm, Stephan Ehl, Charlotte Niemeyer, Marcin W. Wlodarski

Clinical and Molecular Heterogeneity of RTEL1 Deficiency

Carsten Speckmann, Sushree Sangita Sahoo, Marta Rizzi, Shinsuke Hirabayashi, Liliana Annette Rindle, Maximilian Seidl, Anne Rensing-Ehl, Ekkehart Lausch, Brigitte Strahm, Stephan Ehl, Charlotte Niemeyer, Marcin W. Wlodarski · Yayınevi bilinmiyor

Sayfa sayısı yok · 2017

Kategori yok

CiltSynonymous GATA2 Mutations Result in Selective Loss of Mutated RNA and are Common in Patients with GATA2 DeficiencyEmilia J. Kozyra, Victor Bengt Pastor Loyola, Stylianos Lefkopoulos, Sushree Sangita Sahoo, Hauke Busch, Rebecca K. Voss, Miriam Erlacher, Dirk Lebrecht, Amina Szvetnik, Shinsuke Hirabayashi, Patrick Metzger, Melanie Börries, Christian Flotho, Brigitte Strahm, Marcin W. Wlodarski

Synonymous GATA2 Mutations Result in Selective Loss of Mutated RNA and are Common in Patients with GATA2 Deficiency

Emilia J. Kozyra, Victor Bengt Pastor Loyola, Stylianos Lefkopoulos, Sushree Sangita Sahoo, Hauke Busch, Rebecca K. Voss, Miriam Erlacher, Dirk Lebrecht, Amina Szvetnik, Shinsuke Hirabayashi, Patrick Metzger, Melanie Börries, Christian Flotho, · Yayınevi bilinmiyor

CiltConstitutional SAMD9L Mutations Cause Familial Myelodysplastic Syndrome and Transient Monosomy 7Victor Pastor, Sushree Sangita Sahoo, Jessica Boklan, Georg C. Schwabe, Ebru Saribeyoglu, Brigitte Strahm, Dirk Lebrecht, Matthias Voss, Yenan T. Bryceson, Miriam Erlacher, Gerhard Ehninger, Marena Rebekka Niewisch, Brigitte Schlegelberger, Irith Baumann, John C. Achermann, Akiko Shimamura, Jochen Hochrein, Ulf Tedgård, Lars Nilsson, Henrik Hasle, Melanie Börries, Hauke Busch, Charlotte Niemeyer, Marcin W. Wlodarski

Constitutional SAMD9L Mutations Cause Familial Myelodysplastic Syndrome and Transient Monosomy 7

Victor Pastor, · Yayınevi bilinmiyor

Brigitte Strahm,

Marcin W. Wlodarski

Sayfa sayısı yok · 2020

Kategori yok

Sushree Sangita Sahoo,

Jessica Boklan,

Georg C. Schwabe,

Ebru Saribeyoglu,

Brigitte Strahm,

Yenan T. Bryceson,

Miriam Erlacher,

Gerhard Ehninger,

Marena Rebekka Niewisch,

Brigitte Schlegelberger,

John C. Achermann,

Akiko Shimamura,

Jochen Hochrein,

Melanie Börries,

Charlotte Niemeyer,

Marcin W. Wlodarski

Sayfa sayısı yok · 2018

Kategori yok