Fenestra ovalis （oval window）是什么意思，中文意思 | 卵圆窗英文怎么说医学英语中英文词汇翻译

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Inactivation of Bardet-Biedl syndrome genes causes kidney defects

DF Guo, AM Beyer, B Yang… - American Journal of …, 2011 - Am Physiological Soc
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Primary cilia membrane assembly is initiated by Rab11 and transport protein particle II (TRAPPII) complex-dependent trafficking of Rabin8 to the centrosome

[HTML] from pnas.orgCJ Westlake, LM Baye… - Proceedings of the …, 2011 - National Acad Sciences
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Early Decline in Cancer Antigen 125 as a Surrogate for Progression-Free Survival in Recurrent Ovarian Cancer

[HTML] from oxfordjournals.orgCK Lee, M Friedlander, C Brown… - Journal of the …, 2011 - jnci.oxfordjournals.org
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Val/Val genotype of brain-derived neurotrophic factor (BDNF) Val66Met polymorphism is associated with a better response to OROS-MPH in Korean ADHD children

BN Kim, TDR Cummins, JW Kim… - The International …, 2011 - Cambridge Univ Press
... Research Article. Val/Val genotype of brain-derived neurotrophic factor (BDNF) Val
66 Met polymorphism is associated with a better response to OROS-MPH in Korean
ADHD children. Article author query; kim bn [PubMed] [Google ...
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Functional analysis of BBS3 A89V that results in non-syndromic retinal degeneration

[HTML] from nih.govPR Pretorius, MA Aldahmesh… - Human molecular …, 2011 - Oxford Univ Press
... Tel: +1 3193356898; Fax: +1 3193357588; Email: val-sheffield{at}uiowa.edu. Received
December 21, 2010. Accepted January 25, 2011. Next Section. Abstract. Bardet–Biedl
syndrome (BBS) is a syndromic form of retinal degeneration. ...
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Inactivation of Bardet-Biedl syndrome genes causes kidney defects

Primary cilia membrane assembly is initiated by Rab11 and transport protein particle II (TRAPPII) complex-dependent trafficking of Rabin8 to the centrosome

Early Decline in Cancer Antigen 125 as a Surrogate for Progression-Free Survival in Recurrent Ovarian Cancer

Val/Val genotype of brain-derived neurotrophic factor (BDNF) Val66Met polymorphism is associated with a better response to OROS-MPH in Korean ADHD children

Functional analysis of BBS3 A89V that results in non-syndromic retinal degeneration