ECTRODACTYLY IN CHARGE SYNDROME: A RARE PHENOTYPIC FEATURE LINKS CHD7, NIPBL, AND TP63 TO A DEVELOPMENTAL FIELD DEFECT

Martinez-Agosto Julian A.

首页> 外文期刊>American journal of medical genetics, Part A >ECTRODACTYLY IN CHARGE SYNDROME: A RARE PHENOTYPIC FEATURE LINKS CHD7, NIPBL, AND TP63 TO A DEVELOPMENTAL FIELD DEFECT

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ECTRODACTYLY IN CHARGE SYNDROME: A RARE PHENOTYPIC FEATURE LINKS CHD7, NIPBL, AND TP63 TO A DEVELOPMENTAL FIELD DEFECT

机译：电荷综合征中的异常现象：罕见的表型特征将CHD7，NIPBL和TP63链接到发育场缺陷

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《American journal of medical genetics, Part A》 |2015年第8期|共1页
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Martinez-Agosto Julian A.;
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正文语种 eng
中图分类医学遗传学;
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1. ECTRODACTYLY IN CHARGE SYNDROME: A RARE PHENOTYPIC FEATURE LINKS CHD7, NIPBL, AND TP63 TO A DEVELOPMENTAL FIELD DEFECT [J] . Martinez-Agosto Julian A. American journal of medical genetics, Part A . 2015,第8期

机译：电荷综合征中的异常现象：罕见的表型特征将CHD7，NIPBL和TP63链接到发育场缺陷
2. Molecular and phenotypic aspects of CHD7 mutation in CHARGE syndrome. [J] . Zentner GE, Layman WS, Martin DM, American journal of medical genetics, Part A . 2010,第3期

机译：CHARGE综合征中CHD7突变的分子和表型方面。
3. CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene. [J] . Jongmans MC, Admiraal RJ, van der Donk KP, Journal of Medical Genetics . 2006,第4期

机译：CHARGE综合征：CHD7基因突变的表型谱。
4. Charging of PE and XLPE specimens: effect of antioxidant and cross-linking on luminescence features, space charge and conduction current measurements [C] . Montanari, G.C., Teyssedre, Electrical Insulation and Dielectric Phenomena, 2004. CEIDP '04 . 2004

机译：PE和XLPE样品的充电：抗氧化剂和交联对发光特性，空间电荷和传导电流测量的影响
5. Phenotypic Plasticity, Behavioral Syndromes and Their Evolutionary Implications in Pacific Field Cricket Females [D] . Dimitrova, Nadya Dimitrova. 2015

机译：太平洋田Female女性的表型可塑性，行为综合征及其进化意义
6. CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene [O] . M C J Jongmans, R J Admiraal, K P van der Donk, 2006

机译：CHARGE综合征：CHD7基因突变的表型谱
7. Molecular and phenotypic aspects of CHD7 mutation in CHARGE syndrome [O] . Zentner, Gabriel E., Layman, Wanda S., Martin, Donna M., 2010

机译：CHaRGE综合征中CHD7突变的分子和表型方面

ECTRODACTYLY IN CHARGE SYNDROME: A RARE PHENOTYPIC FEATURE LINKS CHD7, NIPBL, AND TP63 TO A DEVELOPMENTAL FIELD DEFECT

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