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1

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/..

2

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/..

3

The Genetic Facets of Dravet Syndrome: Recent Insights:

Mouhi, Hinde El ; Abbassi, Meriame ; Jalte, Meryem...
Annals of Child Neurology. 32 (2024) 2 - p. 67-82 , 2024

Link: https://doi.org/10.26815..

4

Autosomal Dominant Intellectual Development Disorder-6 (MRD..:

El Mouhi, Hinde ; Abbassi, Meriame ; Sayel, Hanane...
Cureus. , 2023

Link: https://doi.org/10.7759/..

5

Clinical characterization of 72 patients with del(22)(q11.2..:

Méndez-Rosado, Luis A. ; de León-Ojeda, Norma ; García, Alina...
Egyptian Journal of Medical Human Genetics. 23 (2022) 1 - p. , 2022

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

6

Near tetrapoloid karyotype with translocation t(11;14) in a..:

Hamdaoui, Hasna ; Natiq, Abdelhafid ; Benlarroubia, Oumaima...
Leukemia Research Reports. 14 (2020) - p. 100217 , 2020

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

7

Variation of exon 11 of the BRCA1 gene in patients with fam..:

Ibrahim Khalil, Ahmadaye ; Bendahhou, Karima ; Rhouda, Taha...
Gene Reports. 12 (2018) - p. 243-247 , 2018

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

8

20p12.3 deletion is rare cause of syndromic cleft palate: c..:

Amasdl, Saadia ; Natiq, Abdelhafid ; Sbiti, Aziza...
BMC Research Notes. 9 (2016) 1 - p. , 2016

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

9

Insulin-like growth factor type 1 deficiency in a Moroccan ..:

Amasdl, Saadia ; Natiq, Abdelhafid ; Elalaoui, Siham Chafai...
Journal of Medical Case Reports. 10 (2016) 1 - p. , 2016

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

10

Hereditary persistence of fetal hemoglobin in two patients ..:

Natiq, Abdelhafid ; Lysy, Philippe A. ; Gillemans, Nynke...
American Journal of Hematology. 92 (2016) 1 - p. , 2016

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

11

Cytotoxicité de la chaînette élastomérique dans la salive a..:

Halimi, Abdelali ; Azeroual, Mohamed-Faouzi ; Eddimani, Latifa...
International Orthodontics. 13 (2015) 1 - p. 16-25 , 2015

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

12

Cytotoxicity of elastomeric power chains in artificial sali..:

Halimi, Abdelali ; Azeroual, Mohamed-Faouzi ; Eddimani, Latifa...
International Orthodontics. 13 (2015) 1 - p. 16-25 , 2015

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

13

A new case of de novo 19p13.2p13.12 deletion in a girl with..:

Natiq, Abdelhafid ; Elalaoui, Siham ; Miesch, Sevrine...
Molecular Cytogenetics. 7 (2014) 1 - p. 40 , 2014

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

14

Tetrasomy 15q11-q13 Diagnosed by FISH in a Patient with Aut..:

Ouldim, Karim ; Natiq, Abdelhafid ; Jonveaux, Philippe.
Journal of Biomedicine and Biotechnology. 2007 (2007) - p. 1-4 , 2007

Link: https://doi.org/10.1155/..

15

Homozygous silencing of T-box transcription factor EOMES le..:

Baala, Lekbir ; Briault, Sylvain ; Etchevers, Heather C...
Nature Genetics. 39 (2007) 4 - p. 454-456 , 2007

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

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