Bone Marrow Failure Syndrome (BMFS) Research 
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This is an RSS file. You can use it to subscribe to this data in your favourite RSS reader or to display this data on your own website or blog.A novel Mecom gene mutation associated with amegakaryocytic thrombocytopenia in a premature infant
CONCLUSIONS: In this report, we present a patient with congenital bone marrow failure successfully treated with haploidentic BMT and describe a novel, de novo pathogenic variant in MECOM gene.PMID:36082647 | DOI:10.24953/turkjped.2021.4855 (Source: The Turkish Journal of Pediatrics)
Source: The Turkish Journal of Pediatrics - September 9, 2022 Category: Pediatrics Authors: Burak Delilo ğlu Özlem Tüfekçi Funda T üzün Ay ça Aykut Emine İpek Ceylan Asude Durmaz Şebnem Yılmaz Nuray Duman Hasan Özkan Hale Ören Source Type: research
A novel Mecom gene mutation associated with amegakaryocytic thrombocytopenia in a premature infant
CONCLUSIONS: In this report, we present a patient with congenital bone marrow failure successfully treated with haploidentic BMT and describe a novel, de novo pathogenic variant in MECOM gene.PMID:36082647 | DOI:10.24953/turkjped.2021.4855 (Source: The Turkish Journal of Pediatrics)
Source: The Turkish Journal of Pediatrics - September 9, 2022 Category: Pediatrics Authors: Burak Delilo ğlu Özlem Tüfekçi Funda T üzün Ay ça Aykut Emine İpek Ceylan Asude Durmaz Şebnem Yılmaz Nuray Duman Hasan Özkan Hale Ören Source Type: research
A novel Mecom gene mutation associated with amegakaryocytic thrombocytopenia in a premature infant
CONCLUSIONS: In this report, we present a patient with congenital bone marrow failure successfully treated with haploidentic BMT and describe a novel, de novo pathogenic variant in MECOM gene.PMID:36082647 | DOI:10.24953/turkjped.2021.4855 (Source: The Turkish Journal of Pediatrics)
Source: The Turkish Journal of Pediatrics - September 9, 2022 Category: Pediatrics Authors: Burak Delilo ğlu Özlem Tüfekçi Funda T üzün Ay ça Aykut Emine İpek Ceylan Asude Durmaz Şebnem Yılmaz Nuray Duman Hasan Özkan Hale Ören Source Type: research
A novel Mecom gene mutation associated with amegakaryocytic thrombocytopenia in a premature infant
CONCLUSIONS: In this report, we present a patient with congenital bone marrow failure successfully treated with haploidentic BMT and describe a novel, de novo pathogenic variant in MECOM gene.PMID:36082647 | DOI:10.24953/turkjped.2021.4855 (Source: The Turkish Journal of Pediatrics)
Source: The Turkish Journal of Pediatrics - September 9, 2022 Category: Pediatrics Authors: Burak Delilo ğlu Özlem Tüfekçi Funda T üzün Ay ça Aykut Emine İpek Ceylan Asude Durmaz Şebnem Yılmaz Nuray Duman Hasan Özkan Hale Ören Source Type: research
A novel Mecom gene mutation associated with amegakaryocytic thrombocytopenia in a premature infant
CONCLUSIONS: In this report, we present a patient with congenital bone marrow failure successfully treated with haploidentic BMT and describe a novel, de novo pathogenic variant in MECOM gene.PMID:36082647 | DOI:10.24953/turkjped.2021.4855 (Source: The Turkish Journal of Pediatrics)
Source: The Turkish Journal of Pediatrics - September 9, 2022 Category: Pediatrics Authors: Burak Delilo ğlu Özlem Tüfekçi Funda T üzün Ay ça Aykut Emine İpek Ceylan Asude Durmaz Şebnem Yılmaz Nuray Duman Hasan Özkan Hale Ören Source Type: research
A novel Mecom gene mutation associated with amegakaryocytic thrombocytopenia in a premature infant
CONCLUSIONS: In this report, we present a patient with congenital bone marrow failure successfully treated with haploidentic BMT and describe a novel, de novo pathogenic variant in MECOM gene.PMID:36082647 | DOI:10.24953/turkjped.2021.4855 (Source: The Turkish Journal of Pediatrics)
Source: The Turkish Journal of Pediatrics - September 9, 2022 Category: Pediatrics Authors: Burak Delilo ğlu Özlem Tüfekçi Funda T üzün Ay ça Aykut Emine İpek Ceylan Asude Durmaz Şebnem Yılmaz Nuray Duman Hasan Özkan Hale Ören Source Type: research
A novel Mecom gene mutation associated with amegakaryocytic thrombocytopenia in a premature infant
CONCLUSIONS: In this report, we present a patient with congenital bone marrow failure successfully treated with haploidentic BMT and describe a novel, de novo pathogenic variant in MECOM gene.PMID:36082647 | DOI:10.24953/turkjped.2021.4855 (Source: The Turkish Journal of Pediatrics)
Source: The Turkish Journal of Pediatrics - September 9, 2022 Category: Pediatrics Authors: Burak Delilo ğlu Özlem Tüfekçi Funda T üzün Ay ça Aykut Emine İpek Ceylan Asude Durmaz Şebnem Yılmaz Nuray Duman Hasan Özkan Hale Ören Source Type: research
A novel Mecom gene mutation associated with amegakaryocytic thrombocytopenia in a premature infant
CONCLUSIONS: In this report, we present a patient with congenital bone marrow failure successfully treated with haploidentic BMT and describe a novel, de novo pathogenic variant in MECOM gene.PMID:36082647 | DOI:10.24953/turkjped.2021.4855 (Source: The Turkish Journal of Pediatrics)
Source: The Turkish Journal of Pediatrics - September 9, 2022 Category: Pediatrics Authors: Burak Delilo ğlu Özlem Tüfekçi Funda T üzün Ay ça Aykut Emine İpek Ceylan Asude Durmaz Şebnem Yılmaz Nuray Duman Hasan Özkan Hale Ören Source Type: research
A novel Mecom gene mutation associated with amegakaryocytic thrombocytopenia in a premature infant
CONCLUSIONS: In this report, we present a patient with congenital bone marrow failure successfully treated with haploidentic BMT and describe a novel, de novo pathogenic variant in MECOM gene.PMID:36082647 | DOI:10.24953/turkjped.2021.4855 (Source: The Turkish Journal of Pediatrics)
Source: The Turkish Journal of Pediatrics - September 9, 2022 Category: Pediatrics Authors: Burak Delilo ğlu Özlem Tüfekçi Funda T üzün Ay ça Aykut Emine İpek Ceylan Asude Durmaz Şebnem Yılmaz Nuray Duman Hasan Özkan Hale Ören Source Type: research
A novel Mecom gene mutation associated with amegakaryocytic thrombocytopenia in a premature infant
CONCLUSIONS: In this report, we present a patient with congenital bone marrow failure successfully treated with haploidentic BMT and describe a novel, de novo pathogenic variant in MECOM gene.PMID:36082647 | DOI:10.24953/turkjped.2021.4855 (Source: The Turkish Journal of Pediatrics)
Source: The Turkish Journal of Pediatrics - September 9, 2022 Category: Pediatrics Authors: Burak Delilo ğlu Özlem Tüfekçi Funda T üzün Ay ça Aykut Emine İpek Ceylan Asude Durmaz Şebnem Yılmaz Nuray Duman Hasan Özkan Hale Ören Source Type: research
A novel Mecom gene mutation associated with amegakaryocytic thrombocytopenia in a premature infant
CONCLUSIONS: In this report, we present a patient with congenital bone marrow failure successfully treated with haploidentic BMT and describe a novel, de novo pathogenic variant in MECOM gene.PMID:36082647 | DOI:10.24953/turkjped.2021.4855 (Source: The Turkish Journal of Pediatrics)
Source: The Turkish Journal of Pediatrics - September 9, 2022 Category: Pediatrics Authors: Burak Delilo ğlu Özlem Tüfekçi Funda T üzün Ay ça Aykut Emine İpek Ceylan Asude Durmaz Şebnem Yılmaz Nuray Duman Hasan Özkan Hale Ören Source Type: research
A novel Mecom gene mutation associated with amegakaryocytic thrombocytopenia in a premature infant
CONCLUSIONS: In this report, we present a patient with congenital bone marrow failure successfully treated with haploidentic BMT and describe a novel, de novo pathogenic variant in MECOM gene.PMID:36082647 | DOI:10.24953/turkjped.2021.4855 (Source: The Turkish Journal of Pediatrics)
Source: The Turkish Journal of Pediatrics - September 9, 2022 Category: Pediatrics Authors: Burak Delilo ğlu Özlem Tüfekçi Funda T üzün Ay ça Aykut Emine İpek Ceylan Asude Durmaz Şebnem Yılmaz Nuray Duman Hasan Özkan Hale Ören Source Type: research
A novel Mecom gene mutation associated with amegakaryocytic thrombocytopenia in a premature infant
CONCLUSIONS: In this report, we present a patient with congenital bone marrow failure successfully treated with haploidentic BMT and describe a novel, de novo pathogenic variant in MECOM gene.PMID:36082647 | DOI:10.24953/turkjped.2021.4855 (Source: The Turkish Journal of Pediatrics)
Source: The Turkish Journal of Pediatrics - September 9, 2022 Category: Pediatrics Authors: Burak Delilo ğlu Özlem Tüfekçi Funda T üzün Ay ça Aykut Emine İpek Ceylan Asude Durmaz Şebnem Yılmaz Nuray Duman Hasan Özkan Hale Ören Source Type: research
A novel Mecom gene mutation associated with amegakaryocytic thrombocytopenia in a premature infant
CONCLUSIONS: In this report, we present a patient with congenital bone marrow failure successfully treated with haploidentic BMT and describe a novel, de novo pathogenic variant in MECOM gene.PMID:36082647 | DOI:10.24953/turkjped.2021.4855 (Source: The Turkish Journal of Pediatrics)
Source: The Turkish Journal of Pediatrics - September 9, 2022 Category: Pediatrics Authors: Burak Delilo ğlu Özlem Tüfekçi Funda T üzün Ay ça Aykut Emine İpek Ceylan Asude Durmaz Şebnem Yılmaz Nuray Duman Hasan Özkan Hale Ören Source Type: research
A novel Mecom gene mutation associated with amegakaryocytic thrombocytopenia in a premature infant
CONCLUSIONS: In this report, we present a patient with congenital bone marrow failure successfully treated with haploidentic BMT and describe a novel, de novo pathogenic variant in MECOM gene.PMID:36082647 | DOI:10.24953/turkjped.2021.4855 (Source: The Turkish Journal of Pediatrics)
Source: The Turkish Journal of Pediatrics - September 9, 2022 Category: Pediatrics Authors: Burak Delilo ğlu Özlem Tüfekçi Funda T üzün Ay ça Aykut Emine İpek Ceylan Asude Durmaz Şebnem Yılmaz Nuray Duman Hasan Özkan Hale Ören Source Type: research
