Intrauterine phenotype features of fetuses with 7q11.23 microduplication syndrome

OBJECTIVE: To share our experience on prenatal diagnosis of 7q11.23 microduplication syndrome and to further delineate the fetal phenotypes of the syndrome. METHODS: A retrospective study was conducted to evaluate seven cases of dup7q11.23 syndrome diagnosed prenatally by chromosomal microarray (CMA...

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Detalles Bibliográficos
Autores principales: Wang, Yunan, Liu, Chang, Hu, Rong, Geng, Juan, Lu, Jian, Zhao, Xin, Xiong, Ying, Wu, Jing, Yin, Aihua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10523695/
https://www.ncbi.nlm.nih.gov/pubmed/37759207
http://dx.doi.org/10.1186/s13023-023-02923-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10523695/
https://www.ncbi.nlm.nih.gov/pubmed/37759207
http://dx.doi.org/10.1186/s13023-023-02923-y

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