Genetic heterogeneity and exclusion of a modifying locus at 17p11.2-p11.1 in Finnish families with van der Woude syndrome.

Wong FK; Koillinen H; Rautio J; Teh BT; Ranta R; Karsten A; Larson O; Linder-Aronson S; Huggare J; Larsson C; Kere J

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Genetic heterogeneity and exclusion of a modifying locus at 17p11.2-p11.1 in Finnish families with van der Woude syndrome.

机译：遗传异质性和17p11.2-p11.1的范德沃德综合征芬兰家庭的修饰位点被排除在外。

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来源
《Journal of Medical Genetics》 |2001年第3期|共5页
作者
Wong FK; Koillinen H; Rautio J; Teh BT; Ranta R; Karsten A; Larson O; Linder-Aronson S; Huggare J; Larsson C; Kere J;
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正文语种 eng
中图分类基础医学;
关键词
Chromosomes; Human; Pair 17; Cleft Lip; 染色体; 人; 17对; 唇裂;

机译：Chromosomes;Human;Pair 17;Cleft Lip;染色体;人;17对;唇裂;

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1. Genetic heterogeneity and exclusion of a modifying locus at 17p11.2-p11.1 in Finnish families with van der Woude syndrome. [J] . Wong FK, Koillinen H, Rautio J, Journal of Medical Genetics . 2001,第3期

机译：遗传异质性和17p11.2-p11.1的范德沃德综合征芬兰家庭的修饰位点被排除在外。
2. Genetic heterogeneity in Van der Woude syndrome: identification of NOL4 and IRF6 haplotype from the noncoding region as candidates in two families [J] . PRIYANKA KUMARI, AKHTAR ALI, SUBODH KUMAR SINGH, Journal of genetics . 2018,第1期

机译：Van der Woude综合征的遗传异质性：从非编码区确定NOL4和IRF6单倍型作为两个家族的候选者
3. Genetic heterogeneity in Van der Woude syndrome: identification of NOL4 and IRF6 haplotype from the noncoding region as candidates in two families [J] . Kumari Priyanka, Ali Akhtar, Singh Subodh Kumar, Journal of genetics . 2018,第1期

机译：Van der Woude综合征的遗传异质性：从非分量区域鉴定NOL4和IRF6单倍型，作为两个家庭的候选者
4. Cardiac Pulse Modeling Using a Modified van der Pol Oscillator and Genetic Algorithms [C] . Fabian M. Lopez-Chamorro, Andres F. Arciniegas-Mejia, David Esteban Imbajoa-Ruiz, International work-conference on bioinformatics and biomedical engineering . 2018

机译：使用改进的van der Pol振荡器和遗传算法的心搏脉冲建模
5. The genetics of insulin resistance in families with polycystic ovary syndrome. [D] . Matar, Jocelyne. 2006

机译：多囊卵巢综合征家庭胰岛素抵抗的遗传学。
6. Genetic heterogeneity and exclusion of a modifying locus at 17p11.2-p11.1 in Finnish families with van der Woude syndrome [O] . F. K. WONG, H. KOILLINEN, J. RAUTIO, 2001

机译：范德沃德综合症芬兰家庭的遗传异质性和17p11.2-p11.1修饰位点的排除
7. Genetic heterogeneity and exclusion of a modifying locus at 17p11.2-p11.1 in Finnish families with van der Woude syndrome [O] . WONG, F. K., KOILLINEN, H., RAUTIO, J., 2001

机译：范德沃德综合症芬兰家庭的遗传异质性和17p11.2-p11.1修饰位点的排除

Genetic heterogeneity and exclusion of a modifying locus at 17p11.2-p11.1 in Finnish families with van der Woude syndrome.

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