Prenatal diagnosis of chromosome 18 long arm deletion syndrome by high-throughput sequencing: Two case reports

RATIONALE: Chromosome 18 long arm deletion syndrome is a group of clinical syndromes caused by partial or total genetic material deletion of the long arm of chromosome 18 (18q), whose clinical manifestations are related to presentation and developmental abnormalities in various aspects such as intel...

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Detalles Bibliográficos
Autores principales: Bai, Xuechun, Zheng, Lianwen, Ma, Shuai, Kan, Xun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
3500
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8677896/
https://www.ncbi.nlm.nih.gov/pubmed/34918667
http://dx.doi.org/10.1097/MD.0000000000028143

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8677896/
https://www.ncbi.nlm.nih.gov/pubmed/34918667
http://dx.doi.org/10.1097/MD.0000000000028143

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