A citation-based method for searching scientific literature

M G Butler. J Intellect Disabil Res 2017
Times Cited: 39

Chih-Ping Chen, Shuan-Pei Lin, Chung-Lin Lee, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Wayseen Wang. Taiwan J Obstet Gynecol 2017
Times Cited: 10

List of shared articles

Times cited

Prenatal diagnosis of a de novo 15q11.2 microdeletion in a maternal inv(4)(p15q31) fetus with increased nuchal translucency: A case report and literature review.
Meiling Sun, Fagui Yue, Yang Yu, Leilei Li, Yuting Jiang, Hongguo Zhang, Ruizhi Liu. Medicine (Baltimore) 2020

Rare missense TUBGCP5 gene variant in a patient with primary microcephaly.
Aleš Maver, Goran Čuturilo, Anja Kovanda, Aleksandra Miletić, Borut Peterlin. Eur J Med Genet 2019

Prenatal diagnosis of a familial 15q11.2 (BP1-BP2) microdeletion encompassing TUBGCP5, CYFIP1, NIPA2 and NIPA1 in a fetus with ventriculomegaly, microcephaly and intrauterine growth restriction on prenatal ultrasound.
Chih-Ping Chen, Shu-Yuan Chang, Liang-Kai Wang, Tung-Yao Chang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Chien-Wen Yang,[...]. Taiwan J Obstet Gynecol 2018

Parent-of-Origin Effects in 15q11.2 BP1-BP2 Microdeletion (Burnside-Butler) Syndrome.
Kyle W Davis, Moises Serrano, Sara Loddo, Catherine Robinson, Viola Alesi, Bruno Dallapiccola, Antonio Novelli, Merlin G Butler. Int J Mol Sci 2019