Tetrasomy 18p: case report and review of literature

Tetrasomy 18p syndrome (Online Mendelian Inheritance in Man 614290) is a very rare chromosomal disorder that is caused by the presence of isochromosome 18p, which is a supernumerary marker composed of two copies of the p arm of chromosome 18. Most tetrasomy 18p cases are de novo cases; however, fami...

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Detalles Bibliográficos
Autores principales: Bawazeer, Shahad, Alshalan, Maha, Alkhaldi, Aziza, AlAtwi, Nasser, AlBalwi, Mohammed, Alswaid, Abdulrahman, Alfadhel, Majid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5811181/
https://www.ncbi.nlm.nih.gov/pubmed/29467581
http://dx.doi.org/10.2147/TACG.S153469

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5811181/
https://www.ncbi.nlm.nih.gov/pubmed/29467581
http://dx.doi.org/10.2147/TACG.S153469

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