Journal of Genetic Medicine : eISSN 2383-8442 / pISSN 1226-1769

Cited by CrossRef (4)

  1. Kuntharee Traisrisilp, Yuri Yanase, Srimeunwai Ake-sittipaisarn, Theera Tongsong. Prenatal Sonographic Features of Cri-du-Chat Syndrome: A Case Report and Analytical Literature Review. Diagnostics 2022;12:421
    https://doi.org/10.3390/diagnostics12020421
  2. Didem Kaymak, Verda Alpay, Hakan Erenel, İbrahim Adaletli, Nil Comunoglu, Riza Madazli. Prenatal Diagnosis of 5p Deletion Syndrome with Brain Abnormalities by Ultrasonography and Fetal Magnetic Resonance Imaging: A Case Report. Fetal and Pediatric Pathology 2020;39:446
    https://doi.org/10.1080/15513815.2019.1669230
  3. Annisa S. L. Mak, Teresa W. L. Ma, Kelvin Y. K. Chan, Anita S. Y. Kan, Mary H. Y. Tang, Kwok Y. Leung. Prenatal diagnosis of 5p deletion syndrome: Report of five cases. J of Obstet and Gynaecol 2019;45:923
    https://doi.org/10.1111/jog.13911
  4. Jiasun Su, Huayu Fu, Bobo Xie, Weiliang Lu, Wei Li, Yuan Wei, Qiang Zhang, Shengkai Wei, Qiuli Chen, Yingchi Lu, Tingting Jiang, Jingsi Luo, Zailong Qin. Prenatal diagnosis of cri-du-chat syndrome by SNP array: report of twelve cases and review of the literature. Mol Cytogenet 2019;12
    https://doi.org/10.1186/s13039-019-0462-0