A citation-based method for searching scientific literature

A novel nonsense mutation in the TCOF1 gene in one Chinese newborn with Treacher Collins syndrome.
Haisheng Zeng, Mingyu Xie, Jianbo Li, Haoqiang Xie, Xiaomei Lu. Int J Pediatr Otorhinolaryngol 2021
Times Cited: 2



First Report of a Single Exon Deletion in TCOF1 Causing Treacher Collins Syndrome.
J Beygo, K Buiting, S Seland, H-J Lüdecke, U Hehr, C Lich, B Prager, D R Lohmann, D Wieczorek. Mol Syndromol 2012
Times Cited: 13




List of shared articles



Times cited

Treacher Collins Syndrome: Genetics, Clinical Features and Management.
Bożena Anna Marszałek-Kruk, Piotr Wójcicki, Krzysztof Dowgierd, Robert Śmigiel. Genes (Basel) 2021
1

Identification of three novel TCOF1 mutations in patients with Treacher Collins Syndrome.
Bożena Anna Marszałek-Kruk, Piotr Wójcicki. Hum Genome Var 2021
1


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