Molecular Cytogenetics | Home page

Molecular Cytogenetics | Home page

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1. A chromosome 1q22 microdeletion including ASH1L is associated with intellectual disability in a Chinese family

   Authors:Hui Xi, Ying Peng, Wanqin Xie, Jialun Pang, Na Ma, Shuting Yang, Jinping Peng and Hua Wang

   Content type:Case Report

    

   4 June 2020

2. Molecular delineation of small supernumerary marker chromosomes using a single nucleotide polymorphism array

   Authors:Lili Zhou, Zhaoke Zheng, Lianpeng Wu, Chenyang Xu, Hao Wu, Xueqin Xu and Shaohua Tang

   Content type:Research

    

   27 May 2020

3. Potential influence of parental copy number variations on noninvasive prenatal testing (NIPT): two case reports

   Authors:Yiming Qi, Jiexia Yang, Yaping Hou, Rong Hu, Dongmei Wang, Haishan Peng and Aihua Yin

   Content type:Case Report

    

   25 May 2020

4. Report of trisomy 2q34-qter and monosomy 4q35.2-qter in a child with mild dysmorphic syndrome and karyotype 46,XY,der(4)t(2;4)(q34;q35.2)pat

   Authors:Juan Pablo Meza-Espinoza, Enrique Sáinz González, Christian J. N. León-León, Eliakym Arámbula-Meraz, José Alfredo Contreras-Gutiérrez, Noemí García-Magallanes, Jesús Madueña-Molina, Fred Luque-Ortega, Salvador Cervín-Serrano and Verónica Judith Picos-Cárdenas

   Content type:Case Report

    

   19 May 2020

5. Dynamic nature of somatic chromosomal mosaicism, genetic-environmental interactions and therapeutic opportunities in disease and aging

   Authors:Svetlana G. Vorsanova, Yuri B. Yurov and Ivan Y. Iourov

   Content type:Hypothesis

    

   7 May 2020