AB097. Clinical and molecular characterization of patients with 6p25 deletion syndrome

OBJECTIVE: Chromosomal imbalances and rearrangements have been implicated in the etiology of intellectual disability and congenital anomalies. Many of these imbalances are caused by submicroscopic deletions or duplications not detected through conventional cytogenetic analysis. The advances in techn...

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Bibliografski detalji
Izdano u:Ann Transl Med
Glavni autori: Lim, Jiin Ying, Jamuar, Saumya Shekhar, Cham, Breana Wen Min, Brett, Maggie, Tan, Ee Shien, Ng, Ivy, Law, Hai Yang, Tan, Ene Choo, Lai, Angeline Hwei Meeng
Format: Artigo
Jezik:Inglês
Izdano: AME Publishing Company 2015
Teme:
Part 4: Oral/poster
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4563479/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3978/j.issn.2305-5839.2015.AB097
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