Literature DB >> 10517681

Waardenburg syndrome.

A L Dourmishev1, L A Dourmishev, R A Schwartz, C K Janniger.   

Abstract

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Mesh：

Year:  1999        PMID： 10517681     DOI： 10.1046/j.1365-4362.1999.00750.x

Source DB:  PubMed          Journal:  Int J Dermatol        ISSN： 0011-9059            Impact factor:   2.736


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  17 in total

Review 1.  Don't it make my blue eyes brown: heterochromia and other abnormalities of the iris.

Authors:  I G Rennie
Journal:  Eye (Lond)       Date:  2011-10-07       Impact factor: 3.775

2.  Waardenburg syndrome: A rare case with bilateral congenital cataract: An unusual entity.

Authors:  Nitin Vichare; N Bhargava
Journal:  Med J Armed Forces India       Date:  2012-12-01

3.  Anisometropic amblyopia in a case of type 2 Waardenburg syndrome.

Authors:  Ali Akal; Tugba Göncü; Nurefsan Boyaci; Ömer Faruk Yılmaz
Journal:  BMJ Case Rep       Date:  2013-12-18

Review 4.  Genetic insights, disease mechanisms, and biological therapeutics for Waardenburg syndrome.

Authors:  Sida Huang; Jian Song; Chufeng He; Xinzhang Cai; Kai Yuan; Lingyun Mei; Yong Feng
Journal:  Gene Ther       Date:  2021-02-25       Impact factor: 4.184

5.  Waardenburg Shah syndrome: A rare case from India.

Authors:  Meenakshi Wadhwani; Yogesh Kumar Gupta; Kulbhushan Gangwani
Journal:  Oman J Ophthalmol       Date:  2015 Jan-Apr

6.  Syndrome in Question.

Authors:  Juliano Peruzzo; Fernanda Luca Nazar; Mariana Quirino Tubone; Gabriela Fortes Escobar; Tania Ferreira Cestari
Journal:  An Bras Dermatol       Date:  2015 Jul-Aug       Impact factor: 1.896

7.  Application of a New Genetic Deafness Microarray for Detecting Mutations in the Deaf in China.

Authors:  Hong Wu; Yong Feng; Lu Jiang; Qian Pan; Yalan Liu; Chang Liu; Chufeng He; Hongsheng Chen; Xueming Liu; Chang Hu; Yiqiao Hu; Lingyun Mei
Journal:  PLoS One       Date:  2016-03-28       Impact factor: 3.240

8.  A novel PAX3 mutation in a Japanese boy with Waardenburg syndrome type 1.

Authors:  Yu Yoshida; Rieko Doi; Kaori Adachi; Eiji Nanba; Isamu Kodani; Kazuo Ryoke
Journal:  Hum Genome Var       Date:  2016-03-03

9.  Analysis of genotype-phenotype relationships in 90 Chinese probands with Waardenburg syndrome.

Authors:  Guojian Wang; Xiaohong Li; Xue Gao; Yu Su; Mingyu Han; Bo Gao; Chang Guo; Dongyang Kang; Shasha Huang; Yongyi Yuan; Pu Dai
Journal:  Hum Genet       Date:  2021-06-17       Impact factor: 4.132

10.  A novel missense mutation of the paired box 3 gene in a Turkish family with Waardenburg syndrome type 1.

Authors:  Filiz Hazan; A Taylan Ozturk; Hamit Adibelli; Nurettin Unal; Ajlan Tukun
Journal:  Mol Vis       Date:  2013-01-29       Impact factor: 2.367
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