Prenatal diagnosis and molecular cytogenetic analyses of a rare 15q21.3 and 16p11.2 microduplication family by Fei Zhang, Gaoqi Liao, Xin Wen, Chengcheng Zhang

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Molecular diagnosis and preimplantation genetic testing for chromosome 1q21.1 recurrent microduplication by Cuiting Peng, Cuiting Peng, Han Chen, Han Chen, Fan Zhou, Fan Zhou, Hong Yang, Hong Yang, Yutong Li, Yutong Li, Yuezhi Keqie, Yuezhi Keqie, Xu Zhao, Xu Zhao, He Wang, He Wang, Ting Hu, Ting Hu, Shanling Liu, Shanling Liu, Jun Ren, Jun Ren, Xinlian Chen, Xinlian Chen

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A novel approach to detecting microduplication in split hand/foot malformation type 3 at the single-cell level: SHFM as a case study by Yaqian Wang, Yang Li, Lidong Zeng, Wenbo Li, Xin Dong, Jia Guo, Xiangrui Meng, Jiacheng Lu, Jiawei Xu

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Case report: Recurrent catatonia in a patient with 17p13.3 microduplication syndrome by Ilya Querter, Ilya Querter, Nika Schuermans, Nele Van de Velde, Cisse Geleyn, Annelies Dheedene, Kurt Audenaert, Kurt Audenaert, Chris Baeken, Chris Baeken, Bert Callewaert, Gilbert Lemmens, Gilbert Lemmens

Subjects: “…17p13.3 microduplication syndrome…”
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The efficacy of expanded non‐invasive prenatal testing (NIPT) in a high‐risk twin pregnancies cohort by Meng Meng, Jianping Chen, Yingjun Yang, Yun Zhang, Gang Zou, Fenhe Zhou, Xing Wei, Yuchun Ge, Jia Zhou, Luming Sun

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A rare intrauterine onset growth retardation syndrome caused by mosaic 19p13.3 microduplication: evaluation of GH/IGF- 1 axis and GH therapy response by Emre Özer, Birsen Karaman, Nilay Güneş, Olcay Evliyaoğlu, Beyhan Tüysüz

Subjects: “…19p13.3 microduplication…”
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Mayer-Rokitansky-Küster-Hauser syndrome associated with 7q11.23 microduplication: A case report by Gabriela Corassa Rodrigues da Cunha, Vanessa Sodré de Souza, Marcus Von Zuben, Mara Santos Córdoba, Mayra Veloso Ayrimoraes Soares, Raphael Severino Bonadio, Daniela Mara de Oliveira, Silviene Fabiana de Oliveira, Juliana Forte de Mazzeu Araújo, Aline Pic-Taylor

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