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Mualla Cetin

Showing results (101-110 of 108) with videos related to

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The Turkish Journal of Pediatrics|March 25, 2011
Hematological consequences of pandemic influenza H1N1 infection: a single center experienceSule Unal, Müge Gökçe, Selin Aytaç-Elmas, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 2, 2005
Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor geneStephan M Tanner, Zhongyuan Li, James D Perko, et al.
Human Mutation|March 17, 2004
Genetically heterogeneous selective intestinal malabsorption of vitamin B12: founder effects, consanguinity, and high clinical awareness explain aggregations in Scandinavia and the Middle EastStephan M Tanner, Zhongyuan Li, Ryan Bisson, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|February 14, 2017
Hematopoietic Stem Cell Transplantation Using Preimplantation Genetic Diagnosis and Human Leukocyte Antigen Typing for Human Leukocyte Antigen-Matched Sibling Donor: A Turkish Multicenter StudyEmin Kurekci, Alphan Küpesiz, Sema Anak, et al.
Blood|June 2, 2005
The mutational spectrum of PTPN11 in juvenile myelomonocytic leukemia and Noonan syndrome/myeloproliferative diseaseChristian P Kratz, Charlotte M Niemeyer, Robert P Castleberry, et al.
Blood|December 10, 2008
LAD-1/variant syndrome is caused by mutations in FERMT3Taco W Kuijpers, Edith van de Vijver, Marian A J Weterman, et al.
Nature Genetics|July 19, 2011
NBEAL2 is mutated in gray platelet syndrome and is required for biogenesis of platelet α-granulesMeral Gunay-Aygun, Tzipora C Falik-Zaccai, Thierry Vilboux, et al.
Blood|August 17, 2010
Gray platelet syndrome: natural history of a large patient cohort and locus assignment to chromosome 3pMeral Gunay-Aygun, Yifat Zivony-Elboum, Fatma Gumruk, et al.
Pageof 11

Showing results (101-110 of 108) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 108 results.
The Turkish Journal of Pediatrics|March 25, 2011
Hematological consequences of pandemic influenza H1N1 infection: a single center experienceSule Unal, Müge Gökçe, Selin Aytaç-Elmas, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 2, 2005
Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor geneStephan M Tanner, Zhongyuan Li, James D Perko, et al.
Human Mutation|March 17, 2004
Genetically heterogeneous selective intestinal malabsorption of vitamin B12: founder effects, consanguinity, and high clinical awareness explain aggregations in Scandinavia and the Middle EastStephan M Tanner, Zhongyuan Li, Ryan Bisson, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|February 14, 2017
Hematopoietic Stem Cell Transplantation Using Preimplantation Genetic Diagnosis and Human Leukocyte Antigen Typing for Human Leukocyte Antigen-Matched Sibling Donor: A Turkish Multicenter StudyEmin Kurekci, Alphan Küpesiz, Sema Anak, et al.
Blood|June 2, 2005
The mutational spectrum of PTPN11 in juvenile myelomonocytic leukemia and Noonan syndrome/myeloproliferative diseaseChristian P Kratz, Charlotte M Niemeyer, Robert P Castleberry, et al.
Blood|December 10, 2008
LAD-1/variant syndrome is caused by mutations in FERMT3Taco W Kuijpers, Edith van de Vijver, Marian A J Weterman, et al.
Nature Genetics|July 19, 2011
NBEAL2 is mutated in gray platelet syndrome and is required for biogenesis of platelet α-granulesMeral Gunay-Aygun, Tzipora C Falik-Zaccai, Thierry Vilboux, et al.
Blood|August 17, 2010
Gray platelet syndrome: natural history of a large patient cohort and locus assignment to chromosome 3pMeral Gunay-Aygun, Yifat Zivony-Elboum, Fatma Gumruk, et al.
Pageof 11