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Blanck, Véronique
24
results:
Search for persons
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Online (24)
Mediatypes
Articles (Online) (8)
OpenAccess-fulltext (16)
Sorted by: Relevance
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?
1
Retrospective analysis and reclassification of DYSF variant..:
Charnay, Théo
;
Blanck, Véronique
;
Cerino, Mathieu
...
Genetics in Medicine. 23 (2021) 8 - p. 1574-1577 , 2021
Link:
https://doi.org/10.1038/..
?
2
Autosomal dominant segregation of CAPN3 c.598_612del15 asso..:
Cerino, Mathieu
;
Bartoli, Marc
;
Riccardi, Florence
...
Annals of Clinical and Translational Neurology. 7 (2020) 12 - p. 2538-2540 , 2020
Link:
https://doi.org/10.1002/..
?
3
Outcomes of 4 years of molecular genetic diagnosis on a pan..:
Grelet, Maude
;
Blanck, Véronique
;
Sigaudy, Sabine
...
Orphanet Journal of Rare Diseases. 14 (2019) 1 - p. , 2019
Link:
https://doi.org/10.1186/..
?
4
Novel heterozygous mutation in ANO3 responsible for cranioc..:
Miltgen, Morgane
;
Blanchard, Arnaud
;
Mathieu, Hélène
...
Movement Disorders. 31 (2016) 8 - p. 1251-1252 , 2016
Link:
https://doi.org/10.1002/..
?
5
Comment on: A novel dysferlin‐mutant pseudoexon bypassed wi..:
Kergourlay, Virginie
;
Blandin, Gaëlle
;
Blanck, Véronique
...
Annals of Clinical and Translational Neurology. 2 (2015) 7 - p. 783-784 , 2015
Link:
https://doi.org/10.1002/..
?
6
Retrospective analysis and reclassification of DYSF variant..:
Charnay, Théo
;
Blanck, Véronique
;
Cerino, Mathieu
...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41436-021-01164-3. , 2021
Link:
https://hal.science/hal-..
?
7
Retrospective analysis and reclassification of DYSF variant..:
Charnay, Théo
;
Blanck, Véronique
;
Cerino, Mathieu
...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41436-021-01164-3. , 2021
Link:
https://hal.science/hal-..
?
8
Retrospective analysis and reclassification of DYSF variant..:
Charnay, Théo
;
Blanck, Véronique
;
Cerino, Mathieu
...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41436-021-01164-3. , 2021
Link:
https://hal.archives-ouv..
?
9
Retrospective analysis and reclassification of DYSF variant..:
Charnay, Théo
;
Blanck, Véronique
;
Cerino, Mathieu
...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41436-021-01164-3. , 2021
Link:
https://amu.hal.science/..
?
10
Novel heterozygous mutation in ANO3 responsible for cranioc..:
Miltgen, Morgane
;
Blanchard, Arnaud
;
Mathieu, Hélène
...
info:eu-repo/semantics/altIdentifier/doi/10.1002/mds.26717. , 2016
Link:
https://hal.science/hal-..
?
11
Novel heterozygous mutation in ANO3 responsible for cranioc..:
Miltgen, Morgane
;
Blanchard, Arnaud
;
Mathieu, Hélène
...
info:eu-repo/semantics/altIdentifier/doi/10.1002/mds.26717. , 2016
Link:
https://hal.science/hal-..
?
12
Novel heterozygous mutation in ANO3 responsible for cranioc..:
Miltgen, Morgane
;
Blanchard, Arnaud
;
Mathieu, Hélène
...
info:eu-repo/semantics/altIdentifier/pmid/27392807. , 2016
Link:
https://hal.archives-ouv..
?
13
Novel heterozygous mutation in ANO3 responsible for cranioc..:
Miltgen, Morgane
;
Blanchard, Arnaud
;
Mathieu, Hélène
...
info:eu-repo/semantics/altIdentifier/doi/10.1002/mds.26717. , 2016
Link:
https://hal.science/hal-..
?
14
Novel heterozygous mutation in ANO3 responsible for cranioc..:
Miltgen, Morgane
;
Blanchard, Arnaud
;
Mathieu, Hélène
...
info:eu-repo/semantics/altIdentifier/doi/10.1002/mds.26717. , 2016
Link:
https://hal.science/hal-..
?
15
Comment on: A novel dysferlin-mutant pseudoexon bypassed wi..:
Kergourlay, Virginie
;
Blandin, Gaëlle
;
Blanck, Veronique
...
info:eu-repo/semantics/altIdentifier/doi/10.1002/acn3.216. , 2015
Link:
https://hal.science/hal-..
1-15