E-LIB Suche - Ergebnisse für: Ilham Ratbi

1

Genome and Epigenome Disorders and Male Infertility: Feedba..:

Montjean, Debbie ; Beaumont, Marion ; Natiq, Abdelhafid...
Genes. 15 (2024) 3 - p. 377 , 2024

Link: https://doi.org/10.3390/..

2

A maternally derived complex small supernumerary marker chr..:

Ouboukss, Fatima ; El Amrani, Zhour ; Bouchahta, Hicham...
Frontiers in Genetics. 15 (2024) - p. , 2024

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

3

Early diagnosis of congenital muscular pathologies using ne..:

El Kadiri, Youssef ; Ratbi, Ilham ; Ouhenach, Mouna...
Egyptian Journal of Medical Human Genetics. 24 (2023) 1 - p. , 2023

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

4

High frequency of hotspot mutation in PTPN11 gene among Mor..:

Ouboukss, Fatima ; Adadi, Najlae ; Amasdl, Saadia...
Journal of Applied Genetics. , 2023

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

5

Mutational spectrum of BRCA1/2 genes in Moroccan patients w..:

Elalaoui, Siham Chafai ; Laarabi, Fatima Zohra ; Afif, Lamiae...
Breast Cancer Research and Treatment. 194 (2022) 1 - p. 187-198 , 2022

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

6

Novel copy number variation of COLQ gene in a Moroccan pati..:

El Kadiri, Youssef ; Ratbi, Ilham ; Sefiani, Abdelaziz.
BMC Neurology. 22 (2022) 1 - p. , 2022

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

7

Clinical and molecular genetic analysis of early-onset myop..:

El Kadiri, Youssef ; Ratbi, Ilham ; Sefiani, Abdelaziz.
Gene Reports. 27 (2022) - p. 101587 , 2022

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

8

Identification of a novel LAMA2 c.2217G > A, p.(Trp739*) mu..:

El Kadiri, Youssef ; Ratbi, Ilham ; Laarabi, Fatima Zahra...
BMC Medical Genomics. 14 (2021) 1 - p. , 2021

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

9

Homozygous nonsense mutation of WTN10B gene in a Moroccan f..:

Elalaoui, Siham Chafai ; Fejjal, Nawfal ; Li, Yun...
Pan African Medical Journal. 39 (2021) - p. , 2021

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

10

Correction to: Rare variants in KDR, encoding VEGF Receptor..:

Škorić-Milosavljević, Doris ; Lahrouchi, Najim ; Bosada, Fernanda M....
Genetics in Medicine. 23 (2021) 10 - p. 2013 , 2021

Link: https://doi.org/10.1038/..

11

Rare variants in KDR, encoding VEGF Receptor 2, are associa..:

Škorić-Milosavljević, Doris ; Lahrouchi, Najim ; Bosada, Fernanda M....
Genetics in Medicine. 23 (2021) 10 - p. 1952-1960 , 2021

Link: https://doi.org/10.1038/..

12

Molecular diagnosis of dystrophinopathies in Morocco and re..:

EL Kadiri, Youssef ; Selouani, Yassir ; Ratbi, Ilham...
Clinica Chimica Acta. 506 (2020) - p. 28-32 , 2020

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

13

First application of next-generation sequencing in patients..:

Adadi, Najlae ; Zrhidri, Abdelali ; Fellat, Ibtissam...
Meta Gene. 22 (2019) - p. 100590 , 2019

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

14

Homozygous frameshift mutations in FAT1 cause a syndrome ch..:

Lahrouchi, Najim ; George, Aman ; Ratbi, Ilham...
Nature Communications. 10 (2019) 1 - p. , 2019

Link: https://doi.org/10.1038/..

15

Post-mortem diagnosis of Pompe disease by exome sequencing ..:

Adadi, Najlae ; Sahli, Maryem ; Egéa, Grégory...
Journal of Medical Case Reports. 12 (2018) 1 - p. , 2018

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