Ich stimme zu, dass diese Seite Cookies verwende. Weitere Informationen finden Sie unter unseren Datenschutzerklärungen .
X
Bloch-Zupan, Agnes
187  Ergebnisse:
Personensuche X
?
1

Diagnosis and management in Rubinstein-Taybi syndrome: firs..:

Lacombe, Didier ; Bloch-Zupan, Agnès ; Bredrup, Cecilie...
Journal of Medical Genetics.  61 (2024)  6 - p. 503-519 , 2024
Link: https://doi.org/10.1136/..
 
?
2

Rare dentin defects: Understanding the pathophysiological m..:

Bugueno, Isaac Maximiliano ; Rey, Tristan ; Jimenez-Armijo, Alexandra...
Genes & Diseases.  11 (2024)  5 - p. 101303 , 2024
Link: https://doi.org/10.1016/..
 
?
3

Biallelic variants in Plexin B2 (PLXNB2) cause amelogenesis..:

Smith, Claire E L ; Laugel-Haushalter, Virginie ; Hany, Ummey...
Journal of Medical Genetics.  61 (2024)  7 - p. 689-698 , 2024
Link: https://doi.org/10.1136/..
 
?
4

The Rogdi knockout mouse is a model for Kohlschütter–Tönz s..:

Jimenez-Armijo, Alexandra ; Morkmued, Supawich ; Ahumada, José Tomás...
Scientific Reports.  14 (2024)  1 - p. , 2024
Link: https://doi.org/10.1038/..
 
?
5

Amelogenesis imperfecta: Next-generation sequencing sheds l..:

Bloch-Zupan, Agnes ; Rey, Tristan ; Jimenez-Armijo, Alexandra...
Frontiers in Physiology.  14 (2023)  - p. , 2023
Link: https://doi.org/10.3389/..
 
?
6

Segmentation, and Numbering in Oral Rare Diseases: Focus on..:

, In: 2023 International Conference on Computational Science and Computational Intelligence (CSCI),
Kadi, Hocine ; Sourget, Theo ; Kawczynski, Marzena... - p. 1358-1363 , 2023
Link: https://doi.org/10.1109/..
 
?
7

Primary failure of eruption: From molecular diagnosis to th..:

Wagner, Delphine ; Rey, Tristan ; Maniere, Marie-Cécile...
Journal of Oral Biology and Craniofacial Research.  13 (2023)  2 - p. 169-176 , 2023
Link: https://doi.org/10.1016/..
 
?
8

Association between malocclusions and amelogenesis imperfec..:

Broutin, Alice ; K Bidi-Lebihan, Angélique ; Canceill, Thibault...
International Orthodontics.  21 (2023)  4 - p. 100789 , 2023
Link: https://doi.org/10.1016/..
 
?
9

GenIDA, a participatory patient registry for genetic forms ..:

Colin, Florent ; Burger, Pauline ; Mazzucotelli, Timothée...
Genetics in Medicine Open.  1 (2023)  1 - p. 100817 , 2023
Link: https://doi.org/10.1016/..
 
?
10

Developmental Defects of the Teeth and Their Hard Tissues:

, In: Pediatric Dentistry; Textbooks in Contemporary Dentistry,
Kotsanos, Nikolaos ; Papagerakis, Petros ; Sarnat, Haim. - p. 415-463 , 2022
Link: https://doi.org/10.1007/..
 
?
11

A Novel Homozygous Variant in GJA1 Causing a Hallermann-Str..:

Jimenez-Armijo, Alexandra ; Oumensour, Khadja ; Bousfiha, Bouchra...
Frontiers in Dental Medicine.  2 (2021)  - p. , 2021
Link: https://doi.org/10.3389/..
 
?
12

COVID-19 and Dentistry in 72 Questions: An Overview of the ..:

Derruau, Stéphane ; Bouchet, Jérôme ; Nassif, Ali...
Journal of Clinical Medicine.  10 (2021)  4 - p. 779 , 2021
Link: https://doi.org/10.3390/..
 
?
13

Deficiency of the SMOC2 matricellular protein impairs bone ..:

Morkmued, Supawich ; Clauss, François ; Schuhbaur, Brigitte...
Scientific Reports.  10 (2020)  1 - p. , 2020
Link: https://doi.org/10.1038/..
 
?
14

A New SLC10A7 Homozygous Missense Mutation Responsible for ..:

Laugel-Haushalter, Virginie ; Bär, Séverine ; Schaefer, Elise...
Frontiers in Genetics.  10 (2019)  - p. , 2019
Link: https://doi.org/10.3389/..
 
?
15

Exome sequencing identifies a novel missense variant in CTS..:

Molitor, Anne ; Prud'homme, Tony ; Miao, Zhichao...
Journal of Human Genetics.  64 (2019)  7 - p. 689-694 , 2019
Link: https://doi.org/10.1038/..
 
1-15