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Pingault, V.
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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...
 
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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...
 
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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...
 
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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...
 
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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...
 
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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/..
 
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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/..
 
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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/..
 
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