Papers: 10.1590/1678-4685-GMB-2016-0049

https://doi.org/10.1590/1678-4685-GMB-2016-0049

1p13.2 deletion displays clinical features overlapping Noonan syndrome, likely related to NRAS gene haploinsufficiency

Cited by: 5
Author(s): Natália Duarte Linhares, Maíra Cristina Menezes Freire, Raony Guimarães Corrêa Do Carmo Lisboa Cardenas, Heloísa B. Pena, Katherine Lachlan, Bruno Dallapiccola, Carlos A. Bacino, Bruno Delobel, Paul James, Ann‐Charlotte Thuresson, Göran Annerén, Sérgio D.J. Pena
Published: almost 9 years ago

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