A New 3p Interstitial Deletion Including the Entire MITF Gene Causes a Variation of Tietz/Waardenburg Type IIA Syndromes

Thomas Schwarzbraun; Lisa Ofner; Gabriele Gillessen-Kaesbach; Barbara Schaperdoth

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A New 3p Interstitial Deletion Including the Entire MITF Gene Causes a Variation of Tietz/Waardenburg Type IIA Syndromes

机译：一个新的3p间隙删除，包括整个MITF基因导致Tietz / Waardenburg IIA型综合征的变异。

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How to cite this article: Schwarzbraun T, Qfner L, Gillessen-Kaesbach G, Schaperdoth B, Preisegger K-H,Windpassinger C, Wagner K, Petek E, Kroisel PM. 2007. A new 3p interstitial deletion including the entireMITFgene causes a variation of Tietz/Waardenburg type IIA syndromes.

机译：如何引用本文：Schwarzbraun T，Qfner L，Gillessen-Kaesbach G，Schaperdoth B，Preisegger K-H，Windpassinger C，Wagner K，Petek E，Kroisel PM。 2007。新的3p间质缺失，包括整个MITFgene，引起Tietz / Waardenburg IIA型综合征的变异。

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《American journal of medical genetics, Part A 》 |2007年第6期| 共6页
作者
Thomas Schwarzbraun; Lisa Ofner; Gabriele Gillessen-Kaesbach; Barbara Schaperdoth;
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正文语种 eng
中图分类医学遗传学 ;
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1. A New 3p Interstitial Deletion Including the Entire MITF Gene Causes a Variation of Tietz/Waardenburg Type IIA Syndromes [J] . Thomas Schwarzbraun, Lisa Ofner, Gabriele Gillessen-Kaesbach, American journal of medical genetics, Part A . 2007 ,第6期

机译：一个新的3p间隙删除，包括整个MITF基因导致Tietz / Waardenburg IIA型综合征的变异。
2. Studies on Pathogenesis of Waardenburg Syndrome Type II and Tietz Syndrome Resulting from MITF Gene Mutations [J] . Zhang Hua, Li Jiada, Luo Hunjin, Journal of Otology . 2013 ,第2期

机译：MITF基因突变导致Waardenburg综合征II型和Tietz综合征的发病机制研究
3. STUDIES ON PATHOGENESIS OF WAARDENBURG SYNDROME TYPE ⅡAND TIETZ SYNDROME RESULTING FROM MITF GENE MUTATIONS [J] . ZHANG Hua, LI Jiada, LUO Hunjin, 中华耳科学杂志（英文版） . 2013 ,第002期

机译：MITF基因突变产生的瓦登堡Ⅱ型综合征和蒂兹综合征的成因研究
4. GENETIC VARIATION AND PHYLOGENETIC RELATIONSHIPS OF PORCINE REPRODUCTIVE AND RESPIRATORY SYNDROME VIRUS (PRRSV) IN CANADA [C] . R. Larochelle, S. DAllaire, P. Raymond, Congress of the International Pig Veterinary Society . 2000

机译：加拿大猪生殖和呼吸综合征病毒（PRRSV）的遗传变异与系统发育关系
5. Chromosomal mapping of genes encoding human Pur-alpha and Pur-beta: Independent and simultaneous deletions in myelodysplastic syndromes and acute myelogenous leukemia. [D] . Lezon-Geyda, Kimberly Ann. 2001

机译：编码人Pur-alpha和Pur-beta的基因的染色体作图：骨髓增生异常综合症和急性骨髓性白血病的独立和同时缺失。
6. Novel mutations including deletions of the entire OFD1 gene in 30 families with type I orofaciodigital syndrome: a study of the extensive clinical variability [O] . Izak J Bisschoff, Christine Zeschnigk, Denise Horn, -1

机译：一种新的突变包括缺失30型orfaciodigital综合征的30个家族中的整个OFD1基因：对广泛的临床变异性的研究
7. Studies on Pathogenesis of Waardenburg Syndrome Type II and Tietz Syndrome Resulting from MITF Gene Mutations [O] . Hua Zhang, Jiada Li, Hunjin Luo, 2013

机译：MITF基因突变导致Waardenburg综合征II型和Tietz综合征的发病机制研究

A New 3p Interstitial Deletion Including the Entire MITF Gene Causes a Variation of Tietz/Waardenburg Type IIA Syndromes

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