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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2003 2
2004 3
2005 5
2006 3
2007 1
2008 3
2009 1
2010 2
2011 1
2012 1
2014 1
2015 4
2016 3
2017 4
2018 4
2019 7
2020 10
2021 3
2022 15
2023 7
2024 7

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84 results

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Page 1
Genotype-Phenotype Correlations in Angelman Syndrome.
Yang L, Shu X, Mao S, Wang Y, Du X, Zou C. Yang L, et al. Among authors: zou c. Genes (Basel). 2021 Jun 28;12(7):987. doi: 10.3390/genes12070987. Genes (Basel). 2021. PMID: 34203304 Free PMC article. Review.
13q22.1-q32.1 Microdeletion Syndrome.
Li MW, Zou XY, Zou CC. Li MW, et al. Indian J Pediatr. 2019 Mar;86(3):303-305. doi: 10.1007/s12098-018-2789-7. Epub 2018 Nov 7. Indian J Pediatr. 2019. PMID: 30406597 No abstract available.
Recommendations for the diagnosis and management of childhood Prader-Willi syndrome in China.
Yang-Li D, Fei-Hong L, Hui-Wen Z, Ming-Sheng M, Xiao-Ping L, Li L, Yi W, Qing Z, Yong-Hui J, Chao-Chun Z; PWS Cooperation Group of Rare Diseases Branch of Chinese Pediatric Society; Zhejiang Expert Group for PWS. Yang-Li D, et al. Orphanet J Rare Dis. 2022 Jun 13;17(1):221. doi: 10.1186/s13023-022-02302-z. Orphanet J Rare Dis. 2022. PMID: 35698200 Free PMC article. Review.
Prader-Willi Syndrome Coincident with DiGeorge Syndrome.
Zou XY, Chao YQ, Zeng LH, Zou CC. Zou XY, et al. Indian J Pediatr. 2020 Jun;87(6):471-472. doi: 10.1007/s12098-019-03137-6. Epub 2019 Dec 20. Indian J Pediatr. 2020. PMID: 31863392 No abstract available.
84 results