E-LIB Suche - Ergebnisse für: Ouertani, Ines

1

3M syndrome: A Tunisian seven-cases series:

Khachnaoui-Zaafrane, Khaoula ; Ouertani, Ines ; Zanati, Amira...
European Journal of Medical Genetics. 65 (2022) 3 - p. 104448 , 2022

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

2

Clinical and genetic characteristics of Tunisian children w..:

El Younsi, Mariem ; Trabelsi, Médiha ; Ben Youssef, Sandra...
Pediatric Nephrology. 38 (2022) 1 - p. 119-129 , 2022

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

3

Le syndrome de Kabuki : étude clinique d'une série de 23 pa..:

Fredj, Hana ; Ouertani, Ines ; Trabelsi, Mediha...
Morphologie. 105 (2021) 350 - p. S33 , 2021

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

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

Novel PAX3 mutations causing Waardenburg syndrome type 1 in..:

Trabelsi, Mediha ; Nouira, Malek ; Maazoul, Faouzi...
International Journal of Pediatric Otorhinolaryngology. 103 (2017) - p. 14-19 , 2017

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

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

Epidemiologic and clinical characteristics of 458 Tunisian ..:

Trabelsi, Mediha ; Chelly, Imen ; Maazoul, Faouzi...
European Journal of Medical Genetics. 56 (2013) 1 - p. 13-19 , 2013

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

9

Hexasomy of the Prader–Willi/Angelman critical region, incl..:

Kraoua, Lilia ; Chaabouni, Myriam ; Ewers, Elisabeth...
European Journal of Medical Genetics. 54 (2011) 4 - p. e446-e450 , 2011

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

10

Prevalence of Bardet–Biedl syndrome in Tunisia:

M'hamdi, Oussama ; Ouertani, Ines ; Maazoul, Faouzi.
Journal of Community Genetics. 2 (2011) 2 - p. 97-99 , 2011

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

11

A 24-Mb deletion in 14q in a girl with corpus callosum hypo..:

Ouertani, Ines ; Chaabouni, Myriam ; Turki, Ilhem...
European Journal of Medical Genetics. 52 (2009) 4 - p. 256-259 , 2009

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

12

Comprehensive PKD1 and PKD2 Mutation Analysis in Prenatal A..:

Audrézet, Marie-Pierre ; Corbiere, Christine ; Lebbah, Said...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4769188/. , 2016

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

13

Targeted high-throughput sequencing for diagnosis of geneti..:

Redin, Claire ; Le Gras, Stéphanie ; Mhamdi, Oussema...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3436454. , 2012

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

14

Prevalence of Bardet–Biedl syndrome in Tunisia:

M'hamdi, Oussama ; Ouertani, Ines ; Maazoul, Faouzi.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3186025. , 2011

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

15

Perinatal-lethal Gaucher disease presenting as hydrops feta..:

Emira Ben Hamida ; Imene Ayadi ; Ines Ouertani...
https://www.panafrican-med-journal.com/content/article/21/110/pdf/110.pdf. , 2015

Link: https://doi.org/10.11604..