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A Novel 4q32.3 Deletion in a Child: Additional Signs and the Role of MARCH1
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| | Xena Giada Pappalardo, Martino Ruggieri, Raffaele Falsaperla, Salvatore Savasta, Umberto Raucci, Piero Pavone | | | Journal of Pediatric Genetics. 2021; 10(04): 259 | | | [Pubmed] [Google Scholar] [DOI] | | | 2 |
Prenatal diagnosis of a 4.5-Mb deletion at chromosome 4q35.1q35.2: Case report and literature review |
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| | Gefei Xiao, Xianrong Qiu, Yuqiu Zhou, Gongjun Tan, Yao Shen | | | Molecular Cytogenetics. 2021; 14(1) | | | [Pubmed] [Google Scholar] [DOI] | | | 3 |
De novo terminal 4q deletion syndrome with new ocular findings in Turkish twins: Case report |
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| | Sandal, G., Ormeci, A.R., Oztas, S. | | | Genetic Counseling. 2013; | | | [Pubmed] [Google Scholar] | | | 4 |
Genotype-phenotype analysis of recombinant chromosome 4 syndrome: an array-CGH study and literature review |
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| | Morteza Hemmat,Omid Hemmat,Arturo Anguiano,Fatih Z Boyar,Mohammed El Naggar,Jia-Chi Wang,Borris T Wang,Trilochan Sahoo,Renius Owen,Mary Haddadin | | | Molecular Cytogenetics. 2013; 6(1): 17 | | | [Pubmed] [Google Scholar] [DOI] | |
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