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Verloes, A.
835
results:
Search for persons
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Format
Online (835)
Mediatypes
Articles (Online) (339)
Bookchapter (Online) (1)
OpenAccess-fulltext (495)
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english (781)
french (37)
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1
Le syndrome ADNP (protéine neuroprotectrice dépendante de l..:
Cravero, C.
;
Gozes, I.
;
Herman, C.
...
Neuropsychiatrie de l'Enfance et de l'Adolescence. 68 (2020) 2 - p. 93-99 , 2020
Link:
https://doi.org/10.1016/..
?
2
Manifestations dermatologiques du syndrome de Costello : ét..:
Bessis, D.
;
Cavé, H.
;
Verloes, A.
.
Annales de Dermatologie et de Vénéréologie. 146 (2019) 12 - p. A253 , 2019
Link:
https://doi.org/10.1016/..
?
3
Manifestations dermatologiques du syndrome cardio-facio-cut..:
Bessis, D.
;
Verloes, A.
;
Cavé, H.
.
Annales de Dermatologie et de Vénéréologie. 146 (2019) 12 - p. A114-A115 , 2019
Link:
https://doi.org/10.1016/..
?
4
Manifestations dermatologiques du syndrome de Noonan: étude..:
Bessis, D.
;
Verloes, A.
;
Geneviève, D.
.
Annales de Dermatologie et de Vénéréologie. 146 (2019) 12 - p. A114 , 2019
Link:
https://doi.org/10.1016/..
?
5
Dermatological manifestations in cardiofaciocutaneous syndr..:
Bessis, D.
;
Morice‐Picard, F.
;
Bourrat, E.
...
British Journal of Dermatology. 180 (2019) 1 - p. e17-e17 , 2019
Link:
https://doi.org/10.1111/..
?
6
心脸皮肤综合症中的皮肤表现:
Bessis, D.
;
Morice‐Picard, F.
;
Bourrat, E.
...
British Journal of Dermatology. 180 (2019) 1 - p. e30-e30 , 2019
Link:
https://doi.org/10.1111/..
?
7
NR4A2 haploinsufficiency is associated with intellectual di..:
Lévy, J.
;
Grotto, S.
;
Mignot, C.
...
Clinical Genetics. 94 (2018) 2 - p. 264-268 , 2018
Link:
https://doi.org/10.1111/..
?
8
Dermatological manifestations in cardiofaciocutaneous syndr..:
Bessis, D.
;
Morice‐Picard, F.
;
Bourrat, E.
...
British Journal of Dermatology. 180 (2018) 1 - p. 172-180 , 2018
Link:
https://doi.org/10.1111/..
?
9
Use and interest of adjustable passive prosthesis (mechanic..:
Martinot-Lagarde, C.
;
Quintero-Prigent, N.
;
Brennetot, N.
...
Annals of Physical and Rehabilitation Medicine. 61 (2018) - p. e327-e328 , 2018
Link:
https://doi.org/10.1016/..
?
10
INTU‐related oral‐facial‐digital syndrome type VI: A confir..:
Bruel, A.‐L.
;
Levy, J.
;
Elenga, N.
...
Clinical Genetics. 93 (2018) 6 - p. 1205-1209 , 2018
Link:
https://doi.org/10.1111/..
?
11
EFNB2haploinsufficiency causes a syndromic neurodevelopment..:
Lévy, J.
;
Haye, D.
;
Marziliano, N.
...
Clinical Genetics. 93 (2018) 6 - p. 1141-1147 , 2018
Link:
https://doi.org/10.1111/..
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12
Autosomal recessive variations of TBX6, from congenital sco..:
Lefebvre, M.
;
Duffourd, Y.
;
Jouan, T.
...
Clinical Genetics. 91 (2017) 6 - p. 908-912 , 2017
Link:
https://doi.org/10.1111/..
?
13
The role of methylation, DNA polymorphisms and microRNAs on..:
Verloes, A.
;
Spits, C.
;
Vercammen, M.
...
Stem Cell Research. 19 (2017) - p. 118-127 , 2017
Link:
https://doi.org/10.1016/..
?
14
Facial dysmorphism is influenced by ethnic background of th..:
Lumaka, A.
;
Cosemans, N.
;
Lulebo Mampasi, A.
...
Clinical Genetics. 92 (2017) 2 - p. 166-171 , 2017
Link:
https://doi.org/10.1111/..
?
15
Refining the phenotypical and mutational spectrum of Taybi‐..:
Putoux, A.
;
Alqahtani, A.
;
Pinson, L.
...
Clinical Genetics. 90 (2016) 6 - p. 550-555 , 2016
Link:
https://doi.org/10.1111/..
1-15