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Blood Cells Molecules And Diseases
(BLOOD CELL MOL DIS) 《血细胞、分子和疾病 》

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Published 2012年10月,Volume 49,Issue 3-4

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Thalassemia
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A novel 506 kb deletion causing εγδβ thalassemia

 Original Research Article
Pages 121-127
Helen Rooks, Barnaby Clark, Steve Best, Peter Rushton, Matthew Oakley, Onn Shaun Thein, Ann C. Cuthbert, Alison Britland, Afruj Ruf, Swee Lay Thein
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Development of a fluorescence immunochromatographic assay for the detection of zeta globin in the blood of (−−SEA) α-thalassemia carriers

 Original Research Article
Pages 128-132
Liyan Wen, Ping Zhu, Yanjun Liu, Qingjun Pan, Yanxia Qu, Xiangmin Xu, Xueli Li, Ning Fu
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Splenectomy is a risk factor for developing hyperuricemia and nephrolithiasis in patients with thalassemia intermedia: A retrospective study

 Original Research Article
Pages 133-135
Paolo Ricchi, Massimiliano Ammirabile, Silvia Costantini, Tiziana Di Matola, Anna Spasiano, Maria Ludovica Genna, Patrizia Cinque, Luciano Prossomariti
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Longitudinal changes in serum ferritin levels correlate with measures of hepatic stiffness in transfusion-independent patients with β-thalassemia intermedia

 Original Research Article
Pages 136-139
Khaled M. Musallam, Irene Motta, Marta Salvatori, Mirella Fraquelli, Alessia Marcon, Ali T. Taher, Maria Domenica Cappellini
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Genetic Disorders
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High resolution melting analysis for the identification of novel mutations in DKC1 and TERT genes in patients with dyskeratosis congenita

 Original Research Article
Pages 140-146
J. Carrillo, P. Martínez, J. Solera, C. Moratilla, A. González, C. Manguán-García, M. Aymerich, L. Canal, M. del Campo, J.L. Dapena, L. Escoda, J.M. García-Sagredo, S. Martín-Sala, S. Rives, J. Sevilla, L. Sastre, R. Perona
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Seven novel genetic mutations within the 5′UTR and the housekeeping promoter of HMBS gene responsible for the non-erythroid form of acute intermittent porphyria

 Original Research Article
Pages 147-151
Valentina Brancaleoni, Francesca Granata, Alessandra Colancecco, Dario Tavazzi, Maria Domenica Cappellini, Elena Di Pierro
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Molecular heterogeneity of glucose-6-phosphate dehydrogenase deficiency in Gaza Strip Palestinians

 Original Research Article
Pages 152-158
Mahmoud Sirdah, N. Scott Reading, Hariprasad Vankayalapati, Sherrie L. Perkins, Mohammad E. Shubair, Lina Aboud, David Roper, Josef T. Prchal
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Umbilical Cord Cell Biology
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A study on mutual interaction between cytokine induced killer cells and umbilical cord-derived mesenchymal cells: Implication for their in-vivo use

 Original Research Article
Pages 159-165
Katia Chieregato, Elena Albiero, Silvia Castegnaro, Martina Bernardi, Emanuele S.G. d'Amore, Cristina Zanon, Domenico Madeo, Francesco Rodeghiero, Giuseppe Astori
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Acute maternal cytomegalovirus infection is associated with significantly decreased numbers of CD34+ cells in umbilical cord blood

 Original Research Article
Pages 166-169
José C. Jaime-Pérez, Julia E. Colunga-Pedraza, Roberto Monreal-Robles, Perla R. Colunga-Pedraza, Nereida Méndez-Ramírez, Rosario Salazar-Riojas, David Gómez-Almaguer
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Myeloproliferative Diseases
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Long term follow up of 93 families with myeloproliferative neoplasms: life expectancy and implications of JAK2V617F in the occurrence of complications

 Original Research Article
Pages 170-176
Sandra Malak, Myriam Labopin, Cecile Saint-Martin, Christine Bellanne-Chantelot, Albert Najman, The French Group of Familial Myeloproliferative Disorders
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