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Annales de genetique最新文献

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Abstracts of the 4th European Cytogenetics Conference. Bologna, Italy, September 6-9, 2003. 第四届欧洲细胞遗传学会议摘要。2003年9月6日至9日，意大利博洛尼亚。
Annales de genetique Pub Date : 2003-09-01
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引用次数: 0
A novel translocation, t(9;21)(q13;q22) rearranging the RUNX1 gene in acute myelomonocytic leukemia. 一个新的易位，t(9;21)(q13;q22)重排RUNX1基因在急性髓细胞白血病。
Annales de genetique Pub Date : 2002-04-01 DOI: 10.1016/S0003-3995(02)01113-9
S. Paulien, O. Maarek, M. Daniel, R. Berger
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引用次数: 6
Dysmorphic Syndromes And Constitutional Diseases Of The Skeleton 畸形综合征和骨骼的体质疾病
Annales de genetique Pub Date : 2002-03-31 DOI: 10.1016/S0003-3995(02)01108-5
C. Stoll
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引用次数: 0
Cytogenetic analysis in 139 Tunisian patients with de novo acute myeloid leukemia. 139例突尼斯新发急性髓性白血病患者的细胞遗传学分析。
Annales de genetique Pub Date : 2002-01-01 DOI: 10.1016/S0003-3995(02)01098-5
H. Sendi, H. Elghezal, Henda Temmi, Haifa Hichri, M. Gribaa, H. Elomri, B. Meddeb, T. Ben Othmane, M. Elloumi, A. Saâd
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引用次数: 16
Evaluation and evolution during time of prenatal diagnosis of congenital heart diseases by routine fetal ultrasonographic examination. 胎儿常规超声检查对先天性心脏病产前诊断的评价与演变。
Annales de genetique Pub Date : 2002-01-01 DOI: 10.1016/S0003-3995(02)01111-5
C. Stoll, B. Dott, Y. Alembik, B. de Geeter
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引用次数: 34
Rhabdomyosarcoma: cytogenetics of five cases using fine-needle aspiration samples and review of the literature. 横纹肌肉瘤:5例细针穿刺样本的细胞遗传学分析及文献复习。
Annales de genetique Pub Date : 2002-01-01 DOI: 10.1016/S0003-3995(02)01103-6
A. Udayakumar, T. Sundareshan, L. Appaji, S. Biswas, G. Mukherjee
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引用次数: 15
HLA polymorphism in type 1 diabetes Tunisians. 1型糖尿病突尼斯人HLA多态性
Annales de genetique Pub Date : 2002-01-01 DOI: 10.1016/S0003-3995(02)01104-8
H. Abid Kamoun, S. Hmida, H. Kaabi, A. Abid, H. Slimane Houissa, M. Maamar, N. Mojâat, L. Ben Hamed, A. Dridi, M. Kamoun Zribi, K. Nagati, A. Haddad, K. Boukef
{"title":"HLA polymorphism in type 1 diabetes Tunisians.","authors":"H. Abid Kamoun, S. Hmida, H. Kaabi, A. Abid, H. Slimane Houissa, M. Maamar, N. Mojâat, L. Ben Hamed, A. Dridi, M. Kamoun Zribi, K. Nagati, A. Haddad, K. Boukef","doi":"10.1016/S0003-3995(02)01104-8","DOIUrl":"https://doi.org/10.1016/S0003-3995(02)01104-8","url":null,"abstract":"","PeriodicalId":7908,"journal":{"name":"Annales de genetique","volume":"1 1","pages":"45-50"},"PeriodicalIF":0.0,"publicationDate":"2002-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89622859","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 24
Linkage disequilibrium and founder effect analysis of the NF1 gene in French Canadians from the Quebec population. 魁北克法裔加拿大人NF1基因连锁不平衡及奠基者效应分析。
Annales de genetique Pub Date : 2002-01-01 DOI: 10.1016/S0003-3995(02)01105-X
L. Fang, Wentian Li, N. Chalhoub, J. Feingold, J. Ortenberg, J. Thirion
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引用次数: 3
Prader-Willi syndrome and polygonosomal abnormalities in males:about a Prader-Willi/47,XYY patient. 普瑞德-威利综合征和男性多性腺体异常:约1名普瑞德-威利/47,XYY患者。
Annales de genetique Pub Date : 2001-01-01 DOI: 10.1016/S0003-3995(01)01039-5
S. Odent, S. Taque, J. Lucas, F. Le Mée, B. Le Marec
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引用次数: 3
Trisomy 5p. A case report and review. 三染色体细胞5 p。个案报告及检讨。
Annales de genetique Pub Date : 2000-12-01 DOI: 10.1016/S0003-3995(00)01030-3
G. Velagaleti, D. Morgan, V. Tonk
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引用次数: 25
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