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Hanene Hannachi
Observed names:
H. Hannachi,
Hannachi Hanene
Institution:
Hôpital Farhat Hached
Observed institutions:
Hôpital Farhat Hached,
University of Sousse
OpenAlex ID:
A5111418581
Phenotype and Micro-array characterization of duplication 11q22.1-q25 and review of the literature
2013
·
Inesse Ben-Abdallah-Bouhjar
, Soumya Mougou-Zerelli
, et al.
·
Gene
·
42
Molecular and Phenotypic Characterization of Ring Chromosome 22 in Two Unrelated Patients
2013
·
H. Hannachi
, S. Mougou
, et al.
·
Cytogenetic and Genome Research
·
41
Chromosomal microarray analysis of functional Xq27-qter disomy and deletion 3p26.3 in a boy with Prader–Willi like features and hypotonia
2012
·
Inesse Ben-Abdallah-Bouhjar
, Hanene Hannachi
, et al.
·
European Journal of Medical Genetics
·
41
Ring chromosome 20 syndrome without deletions of the subtelomeric and CHRNA4–KCNQ2 genes loci
2007
·
Hatem Elghezal
, Hanene Hannachi
, et al.
·
European Journal of Medical Genetics
·
26
Molecular cytogenetic and phenotypic characterization of ring chromosome 13 in three unrelated patients.
2013
·
Inesse B Abdallah-Bouhjar
, Soumaya Mougou-Zerelli
, et al.
·
Europe PMC (PubMed Central)
·
11
Clinical and molecular findings in nine new cases of tetrasomy 18p syndrome: FISH and array CGH characterization
2019
·
Wafa Slimani
, Hela Ben Khelifa
, et al.
·
Molecular Cytogenetics
·
10
PDF
Clinical and Molecular Characterization of a Combined 17p13.3 Microdeletion with Partial Monosomy 21q21.3 in a 26-Year-Old Man
2011
·
H. Hannachi
, S. Mougou-Zerelli
, et al.
·
Cytogenetic and Genome Research
·
6
Chromosomal Microarray Analysis in a Girl With Mental Retardation and Spina Bifida
2010
·
Inesse Ben Abdallah
, Hanene Hannachi
, et al.
·
Pediatric Neurology
·
5
Microarray Analysis of 8p23.1 Deletion in New Patients with Atypical Phenotypical Traits
2015
·
Molka Kammoun
, Hanene Hannachi
, et al.
·
Journal of Pediatric Genetics
·
4
Neuronal migration genes and a familial translocation t (3;17): candidate genes implicated in the phenotype
2020
·
Meriam Hadj Amor
, Sarra Dimassi
, et al.
·
BMC Medical Genetics
·
3
PDF
Cytogenetic analysis in a large series of children with non-syndromic mental retardation
2015
·
Abir Gmidène
, Soumaya Mougou-Zrelli
, et al.
·
Journal of Pediatric Genetics
·
3
Trisomy and tetrasomy 15q11-q13 diagnosed by molecular cytogenetic analysis in two patients with mental retardation
2015
·
Abir Gmidène
, Najla Soyah
, et al.
·
Journal of Pediatric Genetics
·
2
Array Characterization of Prenatally Diagnosed 15q26 Microdeletion and 2q37.1 Duplication: Report of a New Case with Multicystic Kidneys and Review of the Literature
2017
·
Molka Kammoun
, Wafa Slimani
, et al.
·
Journal of Pediatric Genetics
·
1
Genotype-phenotype correlations for the type 1 lissencephaly of eight Tunisian children
2022
·
Meriam Hadj Amor
, Nejla Soyah
, et al.
·
Journal of Clinical Images and Medical Case Reports
PDF
Front & Back Matter
2013
·
E. Kjeldsen
, M. Kallenbach
, et al.
·
Cytogenetic and Genome Research
738 Molecular Characterization of DER (8) (QTERQ21.13: PTERP23.3) Dn In a Child Associating Psychomotor Retardation, Hydrocephalus and Facial Dysmorphism
2012
·
H. Hannachi
, S. Mougou-Zerelli
, et al.
·
Archives of Disease in Childhood
PDF
PP-199. The Jacobsen syndrome: Tow cases report
2010
·
Mougou Soumaya
, Dimassi Sarra
, et al.
·
Early Human Development
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Works count:
17
Citation count:
195
H-index:
6
I10-index:
6
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