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Bacquet, Jean‐Louis
21
results:
Search for persons
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Format
Online (21)
Mediatypes
Articles (Online) (6)
OpenAccess-fulltext (15)
Sorted by: Relevance
Sorted by: Year
?
1
Novel TTLL5 Variants Associated with Cone-Rod Dystrophy and..:
Smirnov, Vasily
;
Grunewald, Olivier
;
Muller, Jean
...
International Journal of Molecular Sciences. 22 (2021) 12 - p. 6410 , 2021
Link:
https://doi.org/10.3390/..
?
2
A case of undiagnosed X-linked retinoschisis presenting as ..:
Cozzupoli, Grazia M
;
Amoroso, Francesca
;
Bacquet, Jean-Louis
...
European Journal of Ophthalmology. 31 (2020) 6 - p. NP65-NP70 , 2020
Link:
https://doi.org/10.1177/..
?
3
Loss of Function of RIMS2 Causes a Syndromic Congenital Con..:
Mechaussier, Sabrina
;
Almoallem, Basamat
;
Zeitz, Christina
...
The American Journal of Human Genetics. 106 (2020) 6 - p. 859-871 , 2020
Link:
https://doi.org/10.1016/..
?
4
Loss of Function of RIMS2 Causes a Syndromic Congenital Con..:
Mechaussier, Sabrina
;
Almoallem, Basamat
;
Zeitz, Christina
...
The American Journal of Human Genetics. 107 (2020) 3 - p. 580 , 2020
Link:
https://doi.org/10.1016/..
?
5
Neither the patient nor the physician could see anything: A..:
Bacquet, Jean‐Louis
;
Weiss, Nicolas
;
Meyniel, Claire
...
American Journal of Hematology. 91 (2016) 8 - p. 858-859 , 2016
Link:
https://doi.org/10.1002/..
?
6
Novel TTLL5 Variants Associated with Cone-Rod Dystrophy and..:
Smirnov, Vasily
;
Grunewald, Olivier
;
Muller, Jean
...
info:eu-repo/semantics/altIdentifier/doi/10.3390/ijms22126410. , 2021
Link:
https://hal.sorbonne-uni..
?
7
Novel TTLL5 Variants Associated with Cone-Rod Dystrophy and..:
Smirnov, Vasily
;
Grunewald, Olivier
;
Muller, Jean
...
info:eu-repo/semantics/altIdentifier/doi/10.3390/ijms22126410. , 2021
Link:
https://hal.sorbonne-uni..
?
8
Novel TTLL5 Variants Associated with Cone-Rod Dystrophy and..:
Smirnov, Vasily
;
Grunewald, Olivier
;
Muller, Jean
...
info:eu-repo/semantics/altIdentifier/doi/10.3390/ijms22126410. , 2021
Link:
https://hal.sorbonne-uni..
?
9
Novel TTLL5 Variants Associated with Cone-Rod Dystrophy and..:
Smirnov, Vasily
;
Grunewald, Olivier
;
Muller, Jean
...
info:eu-repo/semantics/altIdentifier/doi/10.3390/ijms22126410. , 2021
Link:
https://hal.sorbonne-uni..
?
10
Novel TTLL5 Variants Associated with Cone-Rod Dystrophy and..:
Smirnov, Vasily
;
Grunewald, Olivier
;
Muller, Jean
...
info:eu-repo/semantics/altIdentifier/doi/10.3390/ijms22126410. , 2021
Link:
https://hal.sorbonne-uni..
?
11
Loss of Function of RIMS2 Causes a Syndromic Congenital Con..:
Mechaussier, Sabrina
;
Almoallem, Basamat
;
Zeitz, Christina
...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ajhg.2020.04.018. , 2020
Link:
https://hal.science/hal-..
?
12
Loss of Function of RIMS2 Causes a Syndromic Congenital Con..:
Mechaussier, Sabrina
;
Almoallem, Basamat
;
Zeitz, Christina
...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ajhg.2020.04.018. , 2020
Link:
https://hal.science/hal-..
?
13
Loss of Function of RIMS2 Causes a Syndromic Congenital Con..:
Mechaussier, Sabrina
;
Almoallem, Basamat
;
Zeitz, Christina
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7273530/. , 2020
Link:
http://www.ncbi.nlm.nih...
?
14
Loss of Function of RIMS2 Causes a Syndromic Congenital Con..:
Mechaussier, Sabrina
;
Almoallem, Basamat
;
Zeitz, Christina
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7477002/. , 2020
Link:
http://www.ncbi.nlm.nih...
?
15
Loss of Function of RIMS2 Causes a Syndromic Congenital Con..:
Mechaussier, Sabrina
;
Almoallem, Basamat
;
Zeitz, Christina
...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ajhg.2020.04.018. , 2020
Link:
https://hal.science/hal-..
1-15
