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Molecular evidence for full mutations in the FMR1 gene and fragile X syndrome in the Bantu-speaking population in Central Africa
Lubala K., Tonic; Lumaka Zola, Aimé; Shongo, Mick et al.
20152nd Congress of the Congolese Society for Human Genetics
 

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Disciplines :
Neurology
Laboratory medicine & medical technology
Pediatrics
Author, co-author :
Lubala K., Tonic
Lumaka Zola, Aimé  ;  Université de Liège - ULiège > Cancer-Human Genetics
Shongo, Mick
Mbuyi-Musanzayi, Sébastien
Ndua-Musole, M.
Mukuku, Olivier
Yogolelo Asani, Bienvenu
Lubala N.
Kayembe-Kitenge, Tony
Lalamba-Lez
uboya
Devriendt, Koenraad
Lukusa-Tshilobo, Prosper
More authors (3 more) Less
Language :
English
Title :
Molecular evidence for full mutations in the FMR1 gene and fragile X syndrome in the Bantu-speaking population in Central Africa
Publication date :
2015
Event name :
2nd Congress of the Congolese Society for Human Genetics
Event organizer :
Congolese Society for Human Genetics
Event place :
Lubumbashi, Congo - Brazzaville
Event date :
May 11-14, 2015
Available on ORBi :
since 22 January 2020

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