Case report of a novel phenotype in 18q deletion syndrome-Reference-Cited by-同舟云学术

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Case report of a novel phenotype in 18q deletion syndrome

Published:2021-04-01 Issue:3 Volume:61 Page:905-910
ISSN:1220-0522
Container-title:Romanian Journal of Morphology and Embryology
language:
Short-container-title:Rom J Morphol Embryol

Author:

Bohîlţea Roxana Elena, ,Cîrstoiu Monica Mihaela,Nedelea Florina Mihaela,Turcan Natalia,Georgescu Tiberiu Augustin,Munteanu Octavian,Baroş Alexandru,Istrate-Ofiţeru Anca-Maria,Berceanu Costin, , , , , , , , ,

Publisher

Societatea Romana de Morfologie

Subject

Cell Biology,Developmental Biology,Embryology,General Medicine,Pathology and Forensic Medicine

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Terminal microdeletion of chromosome 18 in a Malaysian boy characterized with few features of typical 18q- deletion syndrome: a case report;Journal of Medical Case Reports;2023-06-10

2. Cytogenetic status of patients with congenital malformations or suspected chromosomal abnormalities in Turkey: a comprehensive cytogenetic survey of 11,420 patients;Chromosoma;2022-10-11

3. Prenatal diagnosis of chromosome 18 long arm deletion syndrome by high-throughput sequencing;Medicine;2021-12-17

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