E-LIB Suche - Ergebnisse für: Bacquet, Jean-Louis

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. 107 (2020) 3 - p. 580 , 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. 106 (2020) 6 - p. 859-871 , 2020

Link: https://doi.org/10.1016/..

5

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..

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

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-..

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...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7273530/. , 2020

Link: http://www.ncbi.nlm.nih...

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/PMC7477002/. , 2020

Link: http://www.ncbi.nlm.nih...

14

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-..

15

Destination Memory in Korsakoff's Syndrome:

El Haj, Mohamad ; Kessels, Roy P. C. ; Matton, Christian...
Alcoholism: Clinical and Experimental Research. 40 (2016) 6 - p. 1321-1327 , 2016

Link: https://doi.org/10.1111/..