Deignan, Emily
10  Ergebnisse:
Personensuche X
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1

In vivo analysis of a proprietary glass-based adhesive for ..:

Mehrvar, Cina ; Deignan, Emily ; Hurtig, Mark...
Journal of Materials Science: Materials in Medicine.  32 (2021)  5 - p. , 2021
 
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3

Identification of novel PIEZO1 variants using prenatal exom..:

Datkhaeva, Ilina ; Arboleda, Valerie A. ; Senaratne, T. Niroshi...
American Journal of Medical Genetics Part A.  176 (2018)  12 - p. 2829-2834 , 2018
 
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4

Mutations in ACTL6B Cause Neurodevelopmental Deficits and E..:

Bell, Scott ; Rousseau, Justine ; Peng, Huashan...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ajhg.2019.03.022.  , 2019
 
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5

Mutations in ACTL6B Cause Neurodevelopmental Deficits and E..:

Bell, Scott ; Rousseau, Justine ; Peng, Huashan...
Bell , S , Rousseau , J , Peng , H , Aouabed , Z , Priam , P , Theroux , J-F , Jefri , M , Tanti , A , Wu , H , Kolobova , I , Silviera , H , Manzano-Vargas , K , Ehresmann , S , Hamdan , F F , Hettige , N , Zhang , X , Antonyan , L , Nassif , C , Ghaloul-Gonzalez , L , Sebastian , J , Vockley , J , Begtrup , A G , Wentzensen , I M , Crunk , A , Nicholls , R D , Herman , K C , Deignan , J L , Al-Hertani , W , Efthymiou , S , Salpietro , V , Miyake , N , Makita , Y , Matsumoto , N , Ostern , R , Houge , G , Hafstrom , M , Fassi , E , Houlden , H , Wassink-Ruiter , J S K , Nelson , D , Goldstein , A , Dabir , T , van Gils , J , Bourgeron , T , Delorme , R , Cooper , G M , Martinez , J E , Finnila , C R , Carmant , L , Lortie , A , Oegema , R , van Gassen , K , Mehta , S G , Huhle , D , Abou Jamra , R , Martin , S , Brunner , H G , Lindhout , D , Au , M , Graham , J M , Coubes , C , Turecki , G , Gravel , S , Mechawar , N , Rossignol , E , Michaud , J L , Lessard , J , Ernst ....  , 2019
 
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6

Mutations in ACTL6B Cause Neurodevelopmental Deficits and E..:

Bell, Scott ; Rousseau, Justine ; Peng, Huashan...
https://research.rug.nl/en/publications/fb6a9bbb-1052-4346-8cf3-23b5111f6525.  , 2019
 
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7

Mutations in ACTL6B Cause Neurodevelopmental Deficits and E..:

Bell, Scott ; Rousseau, Justine ; Peng, Huashan...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ajhg.2019.03.022.  , 2019
 
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9

Mutations in ACTL6B Cause Neurodevelopmental Deficits and E..:

Bell, Scott ; Rousseau, Justine ; Peng, Huashan...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ajhg.2019.03.022.  , 2019
 
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