martes, 14 de abril de 2020

Recommendations from Springer Nature

Recommended

Hello Victor Norberto Cerasale Morteo

Here are the latest recommendations for you.
1

Functional study on a novel missense mutation of the transcription factor FOXL2 causes blepharophimosis-ptosis-epicanthus inversus syndrome (BPES)

Fan, J.-Y. ... Fan, X.-Q.
Mutagenesis (2011)
2

Novel FOXL2 mutations in two Chinese families with blepharophimosis-ptosis-epicanthus inversus syndrome

Xue, Min ... Li, Shouling
BMC Medical Genetics (2015)
3

FOXL2 mutations in Indian families with blepharophimosis-ptosis-epicanthus inversus syndrome

Nallathambi, Jeyabalan ... Sundaresan, Periasamy
Journal of Genetics (2007)
4

FOXL2-mutations in blepharophimosis-ptosis-epicanthus inversus syndrome (BPES); challenges for genetic counseling in female patients

Fokstuen, Siv ... Blouin, Jean-Louis
American Journal of Medical Genetics Part A (2002)
5

Heterozygous 17-bp deletion in the forkhead transcription factor gene, FOXL2 , in a Japanese family with blepharophimosis-ptosis-epicanthus inversus syndrome

Yamada, T. ... Endo, M.
Journal of Human Genetics (2001)

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