Elghezal H - Search Results

1

Elghezal H, Alfayez K, Ben Abdallah I, Alfares A, Almazyad A, Al Jasser A, Almobadel N, Alsuhaibani O, Alhashem A. Elghezal H, et al. Eur J Med Genet. 2021 Jul;64(7):104225. doi: 10.1016/j.ejmg.2021.104225. Epub 2021 Apr 16. Eur J Med Genet. 2021. PMID: 33872775

2

De Novo Ring Chromosome 15: Molecular Cytogenetic and Clinical Characterization of First Case from Saudi Arabia.

Alhashem A, Alazmeh S, Barakat A, Alfares A, Elghezal H. Alhashem A, et al. Among authors: elghezal h. J Pediatr Genet. 2020 Dec 2;11(4):320-323. doi: 10.1055/s-0040-1721135. eCollection 2022 Dec. J Pediatr Genet. 2020. PMID: 36267867 Free PMC article.

3

Ring chromosome 20 syndrome without deletions of the subtelomeric and CHRNA4--KCNQ2 genes loci.

Elghezal H, Hannachi H, Mougou S, Kammoun H, Triki C, Saad A. Elghezal H, et al. Eur J Med Genet. 2007 Nov-Dec;50(6):441-5. doi: 10.1016/j.ejmg.2007.07.002. Epub 2007 Aug 6. Eur J Med Genet. 2007. PMID: 17851150

4

Chronic Lymphocytic Leukemia with t(14;18)(q32;q21) As a Sole Cytogenetic Abnormality.

Elyamany G, Fadalla K, Elghezal H, Alsuhaibani O, Osman H, Al-Abulaaly A. Elyamany G, et al. Among authors: elghezal h. Clin Med Insights Pathol. 2014 Sep 23;7:21-7. doi: 10.4137/CPath.S17818. eCollection 2014. Clin Med Insights Pathol. 2014. PMID: 25288894 Free PMC article.

5

Molecular and phenotypic characterization of ring chromosome 22 in two unrelated patients.

Hannachi H, Mougou S, Benabdallah I, Soayh N, Kahloul N, Gaddour N, Le Lorc'h M, Sanlaville D, El Ghezal H, Saad A. Hannachi H, et al. Cytogenet Genome Res. 2013;140(1):1-11. doi: 10.1159/000350785. Epub 2013 Apr 27. Cytogenet Genome Res. 2013. PMID: 23635516

6

Epilepsy, neuropsychiatric phenotypes, neuroimaging findings, and genotype-neurophenotype correlation in 22q11.2 deletion syndrome.

AlKalaf HY, AlHashem AM, AlSaleh NS, AlJohar NM, Abo Thneen AM, ElGhezal HM, Bouhjar IB, Tlili-Graiess K, Sahari AH, Tabarki BM. AlKalaf HY, et al. Among authors: elghezal hm. Neurosciences (Riyadh). 2020 Aug;25(4):287-291. doi: 10.17712/nsj.2020.4.20200045. Neurosciences (Riyadh). 2020. PMID: 33130809 Free PMC article.

7

Chromosomal microarray analysis of functional Xq27-qter disomy and deletion 3p26.3 in a boy with Prader-Willi like features and hypotonia.

Ben-Abdallah-Bouhjar I, Hannachi H, Labalme A, Gmidène A, Mougou S, Soyah N, Gribaa M, Sanlaville D, Elghezal H, Saad A. Ben-Abdallah-Bouhjar I, et al. Among authors: elghezal h. Eur J Med Genet. 2012 Aug-Sep;55(8-9):461-5. doi: 10.1016/j.ejmg.2012.04.011. Epub 2012 Jun 7. Eur J Med Genet. 2012. PMID: 22683462

8

Rare cytogenetic abnormalities and their clinical relevance in pediatric acute leukemia of Saudi Arabian population.

Alkhayat N, Elyamany G, Elborai Y, Sedick Q, Alshahrani M, Al Sharif O, Alenezy A, Hammdan A, Elghezal H, Alsuhaibani O, Aljabry MS, AlMoshary M, Al Mussaed E. Alkhayat N, et al. Among authors: elghezal h. Mol Cytogenet. 2019 Oct 11;12:42. doi: 10.1186/s13039-019-0454-0. eCollection 2019. Mol Cytogenet. 2019. PMID: 31632455 Free PMC article.

9

Clinical and molecular characterization of a combined 17p13.3 microdeletion with partial monosomy 21q21.3 in a 26-year-old man.

Hannachi H, Mougou-Zerelli S, BenAbdallah I, Mama N, Hamdi I, Labalme A, Elghezal H, Sanlaville D, Saad A. Hannachi H, et al. Among authors: elghezal h. Cytogenet Genome Res. 2011;135(2):102-10. doi: 10.1159/000330880. Epub 2011 Aug 26. Cytogenet Genome Res. 2011. PMID: 21876345

10

Chromosomal microarray analysis in a girl with mental retardation and spina bifida.

Ben Abdallah I, Hannachi H, Soyah N, Saad A, Elghezal H. Ben Abdallah I, et al. Among authors: elghezal h. Pediatr Neurol. 2011 Jan;44(1):65-8. doi: 10.1016/j.pediatrneurol.2010.08.015. Pediatr Neurol. 2011. PMID: 21147391

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

62 results

Search Page