A vulnerable point on human chromosome 3 in myeloproliferative disorders?

PHILIP; PREBEN

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A vulnerable point on human chromosome 3 in myeloproliferative disorders?

机译：骨髓增生性疾病中人类3号染色体上的弱点？

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《Hereditas》 |1975年第1期|共2页
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PHILIP; PREBEN;
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正文语种
中图分类遗传学;
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1. Chromosome 20 deletions in myelodysplastic syndromes and Philadelphia-chromosome-negative myeloproliferative disorders: characterization by molecular cytogenetics of commonly deleted and retained regions. [J] . De-Braekeleer M Annals of hematology . 2008,第7期

机译：骨髓增生异常综合症和费城染色体阴性的骨髓增生性疾病中的20号染色体缺失：通过分子细胞遗传学鉴定通常缺失和保留的区域。
2. Chromosome 20 deletions in myelodysplastic syndromes and Philadelphia-chromosome-negative myeloproliferative disorders: characterization by molecular cytogenetics of commonly deleted and retained regions [J] . Nathalie Douet-Guilbert, Audrey Basinko, Frédéric Morel, Annals of Hematology . 2008,第7期

机译：骨髓增生异常综合症和费城染色体阴性的骨髓增生性疾病中的20号染色体缺失：通过分子细胞遗传学鉴定通常缺失和保留的区域
3. Chromosome 21 Gain Is Dispensable for Transient Myeloproliferative Disorder (TMD) Development [J] . Lukes Julius Jr., Potuckova Eliska, Starkova Julia, Blood: The Journal of the American Society of Hematology . 2018,第NovaelaTreatmentAppr期

机译：染色体21增益可分配瞬时肌培养性疾病（TMD）发展
4. Identification of JAK2V617F Mutation on Myeloproliferative Disorders in Medan [C] . Dwi Rita Anggraini, Hidayat, Mega Sari Sitorus Public Health International Conference . 2017

机译：尼曼野生鳞型疾病鉴定JAK2V617F突变
5. Genetic and Epigenetic Alterations within Chromosome 15q11-13.3 Affect Gene Expression in Human Neurodevelopmental Disorders. [D] . Scoles, Haley Anne. 2011

机译：染色体15q11-13.3内的遗传和表观遗传学改变会影响人类神经发育障碍的基因表达。
6. Human tissue-type plasminogen activator gene located near chromosomal breakpoint in myeloproliferative disorder. [O] . T L Yang-Feng, G Opdenakker, G Volckaert, 1986

机译：人组织型纤溶酶原激活基因位于骨髓增生性疾病中的染色体断裂点附近。
7. JAK2V617F-positive polycythemia vera and Philadelphia chromosome-positive chronic myeloid leukemia: one patient with two distinct myeloproliferative disorders [O] . N Cambier, A Renneville, T Cazaentre, 2008

机译：JAK2V617F阳性多胆症Vera和费城染色体阳性慢性骨髓性白血病：一名患有两个不同的髓系紊乱的患者
8. Myeloproliferative Disorder with Unusual Marrow Chromosome Constitution [R] . Whaun, J. M., Lin, C. C., Biederman, B., 1980

机译：具有异常骨髓染色体组成的骨髓增生性疾病

A vulnerable point on human chromosome 3 in myeloproliferative disorders?

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