Prenatal diagnosis of 6pter-p24 deletion syndrome in a fetus from a Han Chinese family: A case report

INTRODUCTION: Chromosome 6pter-p24 deletion syndrome (OMIM #612582) is a rare genetic disorder characterized by deletion of the distal part of 6p. Human 6p deletion syndromes result in a variety of congential malformations. PATIENT CONCERNS: The fetus was the fourth child born to healthy non-consang...

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Detalles Bibliográficos
Autores principales: Shi, Qing-yang, Liu, Yan-hong, Zhang, Yong-sheng, Yu, Xiao-wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2020
Materias:
6700
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7034732/
https://www.ncbi.nlm.nih.gov/pubmed/32080128
http://dx.doi.org/10.1097/MD.0000000000019246

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7034732/
https://www.ncbi.nlm.nih.gov/pubmed/32080128
http://dx.doi.org/10.1097/MD.0000000000019246

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