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Search Results - Novo-Filho, G M
Search Results - Novo-Filho, G M
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A Multicentric Brazilian Investigative Study of Copy Number Variations in Patients with Congenital Anomalies and Intellectual Disability
by
Ceroni, J R M
,
Dutra, R L
,
Honjo, R S
,
Llerena, Jr, J C
,
Acosta, A X
,
Medeiros, P F V
,
Galera, M F
,
Zanardo, É A
,
Piazzon, F B
,
Dias, A T
,
Novo-Filho, G M
,
Montenegro, M M
,
Madia, F A R
,
Bertola, D R
,
de Melo, J B
,
Kulikowski, L D
,
Kim, C A
Published in
Scientific reports
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Application of Whole-Exome Sequencing in Detecting Copy Number Variants in Patients with Developmental Delay and/or Multiple Congenital Malformations
by
Zanardo, Évelin A.
,
Monteiro, Fabíola P.
,
Chehimi, Samar N.
,
Oliveira, Yanca G.
,
Dias, Alexandre T.
,
Costa, Larissa A.
,
Ramos, Luiza L.
,
Novo-Filho, Gil M.
,
Montenegro, Marília M.
,
Nascimento, Amom M.
,
Kitajima, João P.
,
Kok, Fernando
,
Kulikowski, Leslie D.
Published in
The Journal of molecular diagnostics : JMD
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Identifying NAHR mechanism between two distinct Alu elements through breakpoint junction mapping by NGS
by
Novo-Filho, Gil M.
,
Carvalho, Gleyson F.S.
,
Nascimento, Amom M.
,
Montenegro, Marilia M.
,
Damasceno, Jullian G.
,
Zanardo, Évelin A.
,
Chehimi, Samar N.
,
Oliveira, Yanca G.
,
Dias, Alexandre T.
,
Kim, Chong A.
,
Kulikowski, Leslie D.
Published in
Meta Gene
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Alu Elements
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Congenital Defects
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Copy Number
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