Bery, Amandine
42  results:
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4

Recurrent RTTN mutation leading to severe microcephaly, pol..:

Cavallin, Mara ; Bery, Amandine ; Maillard, Camille...
European Journal of Medical Genetics.  61 (2018)  12 - p. 755-758 , 2018
 
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5

TLE1, a key player in neurogenesis, a new candidate gene fo..:

Cavallin, Mara ; Maillard, Camille ; Hully, Marie...
European Journal of Medical Genetics.  61 (2018)  12 - p. 729-732 , 2018
 
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6

Mutations in TBR1 gene leads to cortical malformations and ..:

Vegas, Nancy ; Cavallin, Mara ; Kleefstra, Tjitske...
European Journal of Medical Genetics.  61 (2018)  12 - p. 759-764 , 2018
 
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12

XLF/Cernunnos loss impairs mouse brain development by alter..:

Bery, Amandine ; Etienne, Olivier ; Mouton, Laura...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.celrep.2023.112342.  , 2023
 
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13

XLF/Cernunnos loss impairs mouse brain development by alter..:

Bery, Amandine ; Etienne, Olivier ; Mouton, Laura...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.celrep.2023.112342.  , 2023
 
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14

XLF/Cernunnos loss impairs mouse brain development by alter..:

Bery, Amandine ; Etienne, Olivier ; Mouton, Laura...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.celrep.2023.112342.  , 2023
 
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15

XLF/Cernunnos loss impairs mouse brain development by alter..:

Bery, Amandine ; Etienne, Olivier ; Mouton, Laura...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.celrep.2023.112342.  , 2023
 
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