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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Dades bibliogràfiques
Publicat a:Ann Transl Med
Autors principals: 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
Idioma:Inglês
Publicat: AME Publishing Company 2015
Matèries:
Part 4: Oral/poster
Accés en línia: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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