HIDEA syndrome: A new case report highlighting similarities with ROHHAD syndrome
Harvengt, J, Lumaka, A, Fasquelle, C, Caberg, J H, Mastouri, M, Janssen, A, Palmeira, L, Bours, V
Published in Frontiers in genetics (22.03.2023)
Published in Frontiers in genetics (22.03.2023)
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Facial dysmorphism is influenced by ethnic background of the patient and of the evaluator
Lumaka, A., Cosemans, N., Lulebo Mampasi, A., Mubungu, G., Mvuama, N., Lubala, T., Mbuyi‐Musanzayi, S., Breckpot, J., Holvoet, M., de Ravel, T., Van Buggenhout, G., Peeters, H., Donnai, D., Mutesa, L., Verloes, A., Lukusa Tshilobo, P., Devriendt, K.
Published in Clinical genetics (01.08.2017)
Published in Clinical genetics (01.08.2017)
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Werdnig-Hoffmann disease: report of the first case clinically identified and genetically confirmed in central Africa (Kinshasa-Congo)
Lumaka, A, Bone, D, Lukoo, R, Mujinga, N, Senga, I, Tady, B, Matthijs, G, Lukusa, T P
Published in Genetic counseling (01.01.2009)
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Published in Genetic counseling (01.01.2009)
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GREB1L variants in familial and sporadic hereditary urogenital adysplasia and Mayer‐Rokitansky‐Kuster‐Hauser syndrome
Jacquinet, Adeline, Boujemla, Bouchra, Fasquelle, Corinne, Thiry, Jerôme, Josse, Claire, Lumaka, Aimé, Brischoux‐Boucher, Elise, Dubourg, Christèle, David, Véronique, Pasquier, Laurent, Lehman, Anna, Morcel, Karine, Guerrier, Daniel, Bours, Vincent
Published in Clinical genetics (01.08.2020)
Published in Clinical genetics (01.08.2020)
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Screening of germline mutations in young Rwandan patients with breast cancers
Uyisenga, Jeanne P., Segers, Karin, Lumaka, Aimé Z., Mugenzi, Pacifique, Fasquelle, Corinne, Boujemila, Bouchra, Josse, Claire, Mutesa, Leon, Bours, Vincent
Published in Molecular genetics & genomic medicine (01.11.2020)
Published in Molecular genetics & genomic medicine (01.11.2020)
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