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Pingault, V.
70
results:
Search for persons
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Online (70)
Mediatypes
Articles (Online) (19)
OpenAccess-fulltext (51)
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english (58)
french (3)
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?
1
SATB2-associated syndrome: characterization of skeletal fea..:
Mouillé, M.
;
Rio, M.
;
Breton, S.
...
Orphanet Journal of Rare Diseases. 17 (2022) 1 - p. , 2022
Link:
https://doi.org/10.1186/..
?
2
The association of severe encephalopathy and question mark ..:
Gordon, C.T.
;
Tessier, A.
;
Demir, Z.
...
Clinical Genetics. 93 (2017) 2 - p. 356-359 , 2017
Link:
https://doi.org/10.1111/..
?
3
SOX10 mutations mimic isolated hearing loss:
Pingault, V.
;
Faubert, E.
;
Baral, V.
...
Clinical Genetics. 88 (2014) 4 - p. 352-359 , 2014
Link:
https://doi.org/10.1111/..
?
4
Les mutations SOX10 responsables de l'association des syndr..:
Pingault, V.
;
Bodereau, V.
;
Baral, V.
...
Annales d'Endocrinologie. 74 (2013) 4 - p. 281 , 2013
Link:
https://doi.org/10.1016/..
?
5
Troubles pigmentaires liés à des mutations non tronquantes ..:
Leger, S.
;
Balguerie, X.
;
Goldenberg, A.
...
Annales de Dermatologie et de Vénéréologie. 138 (2011) 12 - p. A70 , 2011
Link:
https://doi.org/10.1016/..
?
6
The SOX10 transcription factor: evaluation as a candidate g..:
Pingault, V.
;
Bondurand, N.
;
Le Caignec, C.
...
Journal of Neurology. 248 (2001) 6 - p. 496-499 , 2001
Link:
https://doi.org/10.1007/..
?
7
A Molecular Analysis of the Yemenite Deaf-Blind Hypopigment..:
Bondurand, N.
;
Kuhlbrodt, K.
;
Pingault, V.
...
Human Molecular Genetics. 8 (1999) 9 - p. 1785-1789 , 1999
Link:
https://doi.org/10.1093/..
?
8
SATB2-associated syndrome: characterization of skeletal fea..:
Mouillé, M
;
Rio, M
;
Breton, S
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8895909/. , 2022
Link:
http://www.ncbi.nlm.nih...
?
9
Spectrum of Temporal Bone Abnormalities in Patients with Wa..:
Elmaleh-Bergès, M
;
Baumann, C
;
Noël-Pétroff, N
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7964579/. , 2013
Link:
http://www.ncbi.nlm.nih...
?
10
Molecular Study of Three Lebanese and Syrian Patients with ..:
Haddad, N.M
;
Ente, D
;
Chouery, E
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3042120. , 2011
Link:
http://www.ncbi.nlm.nih...
?
11
A heterozygous endothelin 3 mutation in Waardenburg-Hirschs..:
PINGAULT, V
;
BONDURAND, N
;
LEMORT, N
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1734825. , 2001
Link:
http://www.ncbi.nlm.nih...
?
12
Neurological phenotype in Waardenburg syndrome type 4 corre..:
Touraine, R L
;
Attié-Bitach, T
;
Manceau, E
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1378013. , 2000
Link:
http://www.ncbi.nlm.nih...
?
13
SATB2-associated syndrome: characterization of skeletal fea..:
M. Mouillé
;
M. Rio
;
S. Breton
...
https://doi.org/10.1186/s13023-022-02229-5. , 2022
Link:
https://doi.org/10.1186/..
?
14
Mother's and children's ADHD genetic risk, household chaos ..:
Agnew‐Blais, Jessica C.
;
Wertz, Jasmin
;
Arseneault, Louise
...
Journal of Child Psychology and Psychiatry. 63 (2022) 10 - p. 1153-1163 , 2022
Link:
https://doi.org/10.1111/..
?
15
Epigenome-wide contributions to individual differences in c..:
Neumann, Alexander
;
Pingault, Jean-Baptiste
;
Felix, Janine F.
...
Clinical Epigenetics. 14 (2022) 1 - p. , 2022
Link:
https://doi.org/10.1186/..
1-15