E-LIB Suche - Ergebnisse für: Meddeb, Rym

1

Constitutional mismatch repair deficiency syndrome with aty..:

Akrout, Firas ; Achour, Ahlem ; Tops, Carli M. J....
Frontiers in Oncology. 13 (2023) - p. , 2023

2

Subchronic toxicity of iron-selenium nanoparticles on oxida..:

Meddeb, El Rym ; Trea, Fouzia ; Djekoun, Abdelmalik..
Environmental Science and Pollution Research. 30 (2023) 52 - p. 112321-112335 , 2023

Link: https://doi.org/10.1007/..

3

Li–Fraumeni syndrome in Tunisian carriers with different an..:

Sassi, Hela ; Meddeb, Rym ; Cherif, Mohamed Aziz...
BMC Medical Genomics. 15 (2022) 1 - p. , 2022

Link: https://doi.org/10.1186/..

4

Le syndrome Wolf–Hirschhorn : à propos de 9 cas:

Fredj, Hana ; Kraoua, Lilia ; Adhoum, Cyrine...
Morphologie. 105 (2021) 350 - p. S28 , 2021

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

5

WDR73-related galloway mowat syndrome with collapsing glome..:

El Younsi, Mariem ; Kraoua, Lilia ; Meddeb, Rym...
European Journal of Medical Genetics. 62 (2019) 9 - p. 103550 , 2019

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

6

Exome sequencing and case–control analyses identify RCC1 as..:

Riahi, Aouatef ; Radmanesh, Hoda ; Schürmann, Peter...
International Journal of Cancer. 142 (2018) 12 - p. 2512-2517 , 2018

Link: https://doi.org/10.1002/..

7

Clinical and Molecular Cytogenetic Study of 38 Williams-Beu..:

Ouertani, Ines ; Chaabouni, Myriam ; Chelly, Imen...
Open Journal of Genetics. 4 (2014) 5 - p. 385-391 , 2014

Link: https://doi.org/10.4236/..

8

Phenotype Spectrum in Tunisian Population with NPHP1 Deleti..:

Hammi, Yousra ; Ferjani, Maryem ; Meddeb, Rym...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10752411/. , 2023

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

9

Constitutional mismatch repair deficiency syndrome with aty..:

Akrout, Firas ; Achour, Ahlem ; Tops, Carli M. J...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10471184/. , 2023

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

10

Li–Fraumeni syndrome in Tunisian carriers with different an..:

Sassi, Hela ; Meddeb, Rym ; Cherif, Mohamed Aziz...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8895785/. , 2022

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

11

Exome sequencing and case-control analyses identify RCC1 as..:

Riahi, Aouatef ; Radmanesh, Hoda ; Schürmann, Peter...
Exome sequencing and case-control analyses identify RCC1 as a candidate breast cancer susceptibility gene. 2018, 142 (12):2512-2517 Int. J. Cancer. , 2018

Link: http://hdl.handle.net/10..

12

Table_1_Constitutional mismatch repair deficiency syndrome ..:

Firas Akrout ; Ahlem Achour ; Carli M. J. Tops...
doi:10.3389/fonc.2023.1195814.s001. , 2023

Link: https://doi.org/10.3389/..

13

Constitutional mismatch repair deficiency syndrome with aty..:

Firas Akrout ; Ahlem Achour ; Carli M. J. Tops...
https://www.frontiersin.org/articles/10.3389/fonc.2023.1195814/full. , 2023

Link: https://doi.org/10.3389/..

14

Li–Fraumeni syndrome in Tunisian carriers with different an..:

Hela Sassi ; Rym Meddeb ; Mohamed Aziz Cherif...
https://doi.org/10.1186/s12920-022-01189-w. , 2022

Link: https://doi.org/10.1186/..

15

Aetiology of Vascular Purpura in a Single Centre Experience..:

Bouslama, Kamel ; Toujani, Sana ; Larbi, Thara...
Mediterranean Journal of Rheumatology. 35 (2024) 1 - p. 94 , 2024

Link: https://doi.org/10.31138..