Literature DB >> 15355442

Genetic basis of Prader-Willi syndrome in Korea: less uniparental disomy than has been recognized?

H-J Kim, H-J Cho, D-K Jin, E-K Kwon, C-S Ki, J-W Kim, S-H Kim.   

Abstract

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Year:  2004        PMID： 15355442     DOI： 10.1111/j.1399-0004.2004.00323.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  4 in total

Review 1.  Recommendations for the diagnosis and management of childhood Prader-Willi syndrome in China.

Authors:  Dai Yang-Li; Luo Fei-Hong; Zhang Hui-Wen; Ma Ming-Sheng; Luo Xiao-Ping; Liu Li; Wang Yi; Zhou Qing; Jiang Yong-Hui; Zou Chao-Chun
Journal:  Orphanet J Rare Dis       Date:  2022-06-13       Impact factor: 4.303

2.  Clinical and genetic features of Prader-Willi syndrome in China.

Authors:  Wei Lu; Yan Qi; Bing Cui; Xiu-Li Chen; Bing-Bing Wu; Chao Chen; Yun Cao; Wen-Hao Zhou; Hong Xu; Fei-Hong Luo
Journal:  Eur J Pediatr       Date:  2013-08-11       Impact factor: 3.183

3.  Sleep-disordered breathing and genetic findings in children with Prader-Willi syndrome in China.

Authors:  Aizhen Lu; Feihong Luo; Chengjun Sun; Xiaobo Zhang; Libo Wang; Wei Lu
Journal:  Ann Transl Med       Date:  2020-08

4.  Clinical Utility of Methylation-Specific Multiplex Ligation-Dependent Probe Amplification for the Diagnosis of Prader-Willi Syndrome and Angelman Syndrome.

Authors:  Boram Kim; Yongsook Park; Sung Im Cho; Man Jin Kim; Jong-Hee Chae; Ji Yeon Kim; Moon-Woo Seong; Sung Sup Park
Journal:  Ann Lab Med       Date:  2022-01-01       Impact factor: 3.464
  4 in total

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