The genotype and phenotype of chromosome 18p deletion syndrome: Case series

RATIONALE: The chromosome 18p deletion syndrome is a syndrome with a deletion of all or a portion of the short arm of the chromosome 18. The phenotypes of the chromosome 18p deletion syndrome vary widely among individuals due to differences in size and breakpoints and the involved genes on the delet...

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Detalles Bibliográficos
Autores principales: Jin, Qiujie, Qiang, Rong, Cai, Bo, Wang, Xiaobin, Cai, Na, Zhen, Shuai, Zhai, Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
3500
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8104293/
https://www.ncbi.nlm.nih.gov/pubmed/33950970
http://dx.doi.org/10.1097/MD.0000000000025777

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8104293/
https://www.ncbi.nlm.nih.gov/pubmed/33950970
http://dx.doi.org/10.1097/MD.0000000000025777

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