Molecular Cytogenetics | Home page

Molecular Cytogenetics | Home page

Molecular Cytogenetics

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1. Prenatal diagnosis of cri-du-chat syndrome by SNP array: report of twelve cases and review of the literature

   Authors:Jiasun Su, Huayu Fu, Bobo Xie, Weiliang Lu, Wei Li, Yuan Wei, Qiang Zhang, Shengkai Wei, Qiuli Chen, Yingchi Lu, Tingting Jiang, Jingsi Luo and Zailong Qin

   Content type:Case Report

   9 December 2019

2. Targeted capture enrichment followed by NGS: development and validation of a single comprehensive NIPT for chromosomal aneuploidies, microdeletion syndromes and monogenic diseases

   Authors:George Koumbaris, Achilleas Achilleos, Michalis Nicolaou, Charalambos Loizides, Kyriakos Tsangaras, Elena Kypri, Petros Mina, Carolina Sismani, Voula Velissariou, Georgia Christopoulou, Pantelis Constantoulakis, Emmanouil Manolakos, Ioannis Papoulidis, Danai Stambouli, Marios Ioannides and Philippos Patsalis

   Content type:Research

   21 November 2019

3. Jumping translocations of chromosome 1q occurring by a multi-stage process in an acute myeloid leukemia progressed from myelodysplastic syndrome with a TET2 mutation

   Authors:Ina Lee, Mary A. Gudipati, Elizabeth Waters, Vu H. Duong, Maria R. Baer and Ying Zou

   Content type:Case Report

   19 November 2019

4. Nonclonal chromosomal alterations and poor survival in cytopenic patients without hematological malignancies

   Authors:Osamu Imataki, Hiroyuki Kubo, Akihiro Takeuchi, Makiko Uemura and Norimitsu Kadowaki

   Content type:Research

   12 November 2019

5. Prenatal diagnosis of 4953 pregnant women with indications for genetic amniocentesis in Northeast China

   Authors:Rulin Dai, Yang Yu, Qi Xi, Xiaonan Hu, Haibo Zhu, Ruizhi Liu and Ruixue Wang

   Content type:Research

   6 November 2019