Works matching AU Barakat, Abdelhamid

Results: 65

First report of an Ivorian family with nonsyndromic hearing loss caused by GJB2 compound heterozygous variants.

Published in:

Annals of Human Genetics, 2025, v. 89, n. 4, p. 135, doi. 10.1111/ahg.12574

By:

Toure, Madoussou;
Amalou, Ghita;
Raise, Imane Ait;
Mobio, N'kan Max Ange;
Malki, Abderrahim;
Barakat, Abdelhamid

Publication type:

Article

Chromosomal abnormalities in couples with recurrent spontaneous miscarriage: a 21-year retrospective study, a report of a novel insertion, and a literature review.

Published in:

Journal of Assisted Reproduction & Genetics, 2019, v. 36, n. 3, p. 499, doi. 10.1007/s10815-018-1373-4

By:

Elkarhat, Zouhair;
Kindil, Zineb;
Zarouf, Latifa;
Razoki, Lunda;
Aboulfaraj, Jamila;
Elbakay, Chadli;
Nassereddine, Sanaa;
Nasser, Boubker;
Barakat, Abdelhamid;
Rouba, Hassan

Publication type:

Article

Whole exome sequencing reveals ABCD1 variant as a potential contributor to male infertility.

Published in:

Molecular Biology Reports, 2025, v. 52, n. 1, p. 1, doi. 10.1007/s11033-025-10234-7

By:

Redouane, Salaheddine;
Harmak, Houda;
El Hamouchi, Adil;
Charoute, Hicham;
Louanjli, Noureddine;
Malki, Abderrahim;
Barakat, Abdelhamid;
Rouba, Hassan

Publication type:

Article

Exome sequencing reveals pathogenic mutations in the LARS2 and HSD17B4 genes associated with Perrault syndrome and D-bifunctional protein deficiency in Moroccan families.

Published in:

Molecular Biology Reports, 2024, v. 51, n. 1, p. 1, doi. 10.1007/s11033-024-09740-x

By:

Idyahia, Assia;
Redouan, Salaheddine;
Amalou, Ghita;
Charoute, Hicham;
Harmak, Houda;
Bonnet, Crystel;
Petit, Christine;
Benrahma, Houda;
Barakat, Abdelhamid

Publication type:

Article

Mediterranean Founder Mutation Database (MFMD): Taking Advantage from Founder Mutations in Genetics Diagnosis, Genetic Diversity and Migration History of the Mediterranean Population.

Published in:

Human Mutation, 2015, v. 36, n. 11, p. E2441, doi. 10.1002/humu.22835

By:

Charoute, Hicham;
Bakhchane, Amina;
Benrahma, Houda;
Romdhane, Lilia;
Gabi, Khalid;
Rouba, Hassan;
Fakiri, Malika;
Abdelhak, Sonia;
Lenaers, Guy;
Barakat, Abdelhamid

Publication type:

Article

In Silico Analysis of Coding/Noncoding SNPs of Human RETN Gene and Characterization of Their Impact on Resistin Stability and Structure.

Published in:

Journal of Diabetes Research, 2019, p. 1, doi. 10.1155/2019/4951627

By:

Elkhattabi, Lamiae;
Morjane, Imane;
Charoute, Hicham;
Amghar, Soumaya;
Bouafi, Hind;
Elkarhat, Zouhair;
Saile, Rachid;
Rouba, Hassan;
Barakat, Abdelhamid

Publication type:

Article

GNE Myopathy and Duchenne Muscular Dystrophy in Two Moroccans Families.

Published in:

Muscles, Ligaments & Tendons Journal (MLTJ), 2023, v. 13, n. 4, p. 653, doi. 10.32098/mltj.04.2023.18

By:

Sifeddine, Najat;
Amalou, Ghita;
Charif, Majida;
Nahili, Halima;
Bouzidi, Ayman;
Salaheddine, Redouane;
Morjane, Iman;
Zouiri, Ghizlane;
Kriouile, Yamna;
Elkhalfi, Bouchra;
Lenaers, Guy;
Barakat, Abdelhamid

Publication type:

Article

The 752delG26 mutation in the RFXANK gene associated with major histocompatibility complex class II deficiency: evidence for a founder effect in the Moroccan population.

Published in:

2010

By:

Naamane, Hamid;
El Maataoui, Ouafaa;
Ailal, Fatima;
Barakat, Abdelhamid;
Bennani, Siham;
Najib, Jilali;
Hassar, Mohammed;
Saile, Rachid;
Bousfiha, Ahmed Aziz

Publication type:

journal article

Screening of exon 11 of BRCA1 gene using the high resolution melting approach for diagnosis in Moroccan breast cancer patients.

Published in:

BMC Cancer, 2015, v. 15, n. 1, p. 1, doi. 10.1186/s12885-015-1040-4

By:

El Khachibi, Meryam;
Diakite, Brehima;
Hamzi, Khalil;
Badou, Abdallah;
Senhaji, Mohamed Amine;
Bakhchane, Amina;
Jouhadi, Hassan;
Barakat, Abdelhamid;
Benider, Abdellatif;
Nadifi, Sellama

Publication type:

Article

Clinicopathological Features and Molecular Analysis of Primary Glioblastomas in Moroccan Patients.

Published in:

Journal of Molecular Neuroscience, 2013, v. 49, n. 3, p. 567, doi. 10.1007/s12031-012-9868-4

By:

Hilmani, Said;
Abidi, Omar;
Benrahma, Houda;
Karkouri, Mehdi;
Sahraoui, Souha;
Azhari, Abdessamad;
Barakat, Abdelhamid

Publication type:

Article

Evidence for Association of the E23K Variant of KCNJ11 Gene with Type 2 Diabetes in Tunisian Population: Population-Based Study and Meta-Analysis.

Published in:

2014

By:

Lasram, Khaled;
Ben Halim, Nizar;
Hsouna, Sana;
Kefi, Rym;
Arfa, Imen;
Ghazouani, Welid;
Jamoussi, Henda;
Benrahma, Houda;
Kharrat, Najla;
Rebai, Ahmed;
Ben Ammar, Slim;
Bahri, Sonia;
Barakat, Abdelhamid;
Abid, Abdelmajid;
Abdelhak, Sonia

Publication type:

Journal Article

Evidence for Association of the E23K Variant of KCNJ11 Gene with Type 2 Diabetes in Tunisian Population: Population-Based Study and Meta-Analysis.

Published in:

BioMed Research International, 2014, v. 2014, p. 1, doi. 10.1155/2014/265274

By:

Lasram, Khaled;
Halim, Nizar Ben;
Hsouna, Sana;
Kefi, Rym;
Arfa, Imen;
Ghazouani, Welid;
Jamoussi, Henda;
Benrahma, Houda;
Kharrat, Najla;
Rebai, Ahmed;
Ammar, Slim Ben;
Bahri, Sonia;
Barakat, Abdelhamid;
Abid, Abdelmajid;
Abdelhak, Sonia

Publication type:

Article

H Syndrome: Two new morrocan cases.

Published in:

Our Dermatology Online / Nasza Dermatologia Online, 2022, v. 13, p. 49, doi. 10.7241/ourd.2022S2.6

By:

Marmech, Cyrine;
El Fetouaki, Fatima Zahra;
Barakat, Abdelhamid;
Skalli, Hayat;
Chiheb, Soumiya

Publication type:

Article

H Syndrome: Two new morrocan cases.

Published in:

Our Dermatology Online / Nasza Dermatologia Online, 2022, v. 13, p. 49, doi. 10.7241/ourd.2022S2.6

By:

Marmech, Cyrine;
El Fetouaki, Fatima Zahra;
Barakat, Abdelhamid;
Skalli, Hayat;
Chiheb, Soumiya

Publication type:

Article

Association of Spermatogenic Failure with the b2/b3 Partial AZFc Deletion.

Published in:

PLoS ONE, 2012, v. 7, n. 4, p. 1, doi. 10.1371/journal.pone.0034902

By:

Eloualid, Abdelmajid;
Rhaissi, Houria;
Reguig, Ahmed;
Bounaceur, Safaa;
houate, Brahim El;
Abidi, Omar;
Charif, Majida;
Louanjli, Noureddine;
Chadli, Elbakkay;
Barakat, Abdelhamid;
Bashamboo, Anu;
McElreavey, Ken;
Rouba, Hassan

Publication type:

Article

Association of the MTHFR A1298C Variant with Unexplained Severe Male Infertility.

Published in:

PLoS ONE, 2012, v. 7, n. 3, p. 1, doi. 10.1371/journal.pone.0034111

By:

Eloualid, Abdelmajid;
Abidi, Omar;
Charif, Majida;
houate, Brahim El;
Benrahma, Houda;
Louanjli, Noureddine;
Chadli, Elbakkay;
Ajjemami, Maria;
Barakat, Abdelhamid;
Bashamboo, Anu;
McElreavey, Ken;
Rhaissi, Houria;
Rouba, Hassan

Publication type:

Article

Novel variants of mitochondrial DNA associated with Type 2 diabetes mellitus in Moroccan population.

Published in:

Mitochondrial DNA. Part A, 2018, v. 29, n. 1, p. 9, doi. 10.1080/24701394.2016.1233530

By:

Charoute, Hicham;
Kefi, Rym;
Bounaceur, Safaa;
Benrahma, Houda;
Reguig, Ahmed;
Kandil, Mostafa;
Rouba, Hassan;
Bakhchane, Amina;
Abdelhak, Sonia;
Barakat, Abdelhamid

Publication type:

Article

Association of HNF1A gene variants and haplotypes with metabolic syndrome: a case–control study in the Tunisian population and a meta-analysis.

Published in:

Diabetology & Metabolic Syndrome, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13098-022-00794-0

By:

Dallali, Hamza;
Hechmi, Meriem;
Morjane, Imane;
Elouej, Sahar;
Jmel, Haifa;
Ben Halima, Yosra;
Abid, Abdelmajid;
Bahlous, Afef;
Barakat, Abdelhamid;
Jamoussi, Henda;
Abdelhak, Sonia;
Kefi, Rym

Publication type:

Article

Cytogenetic profile of patients with clinical spectrum of ambiguous genitalia, amenorrhea, and Turner phenotype: A 21‐year single‐center experience.

Published in:

American Journal of Medical Genetics. Part A, 2019, v. 179, n. 8, p. 1516, doi. 10.1002/ajmg.a.61257

By:

Elkarhat, Zouhair;
Belkady, Boutaina;
Charoute, Hicham;
Zarouf, Latifa;
Razoki, Lunda;
Aboulfaraj, Jamila;
Nassereddine, Sanaa;
Elbakay, Chadli;
Nasser, Boubker;
Barakat, Abdelhamid;
Rouba, Hassan

Publication type:

Article

Contribution of CDKAL1 rs7756992 and IGF2BP2 rs4402960 polymorphisms in type 2 diabetes, diabetic complications, obesity risk and hypertension in the Tunisian population 在突尼斯人群中， CDKAL1 rs7756992与 IGF2BP2 rs4402960的多态性对2型糖尿病、糖尿病并发症、肥胖风险以及高血压的影响

Published in:

Journal of Diabetes, 2015, v. 7, n. 1, p. 102, doi. 10.1111/1753-0407.12147

By:

Lasram, Khaled;
Ben Halim, Nizar;
Benrahma, Houda;
Mediene ‐ Benchekor, Sounnia;
Arfa, Imen;
Hsouna, Sana;
Kefi, Rym;
Jamoussi, Henda;
Ben Ammar, Slim;
Bahri, Sonia;
Abid, Abdelmajid;
Benhamamouch, Soraya;
Barakat, Abdelhamid;
Abdelhak, Sonia

Publication type:

Article

Clinical and genetic spectrums of 413 North African families with inherited retinal dystrophies and optic neuropathies.

Published in:

2022

By:

Bouzidi, Aymane;
Charoute, Hicham;
Charif, Majida;
Amalou, Ghita;
Kandil, Mostafa;
Barakat, Abdelhamid;
Lenaers, Guy

Publication type:

journal article

A novel mutation in the ABCD1 gene of a Moroccan patient with X-linked adrenoleukodystrophy: case report.

Published in:

2015

By:

Karkar, Adnane;
Barakat, Abdelhamid;
Bakhchane, Amina;
Fettah, Houda;
Slassi, Ilham;
Dorboz, Imen;
Boespflug-Tanguy, Odile;
Nadifi, Sellama

Publication type:

journal article

Clinical and genetic investigations of three Moroccan families with retinitis pigmentosa phenotypes.

Published in:

Molecular Vision, 2021, v. 27, p. 17

By:

Bouzidi, Aymane;
Charif, Majida;
Bouzidi, Adil;
Amalou, Ghita;
Kandil, Mostafa;
Barakat, Abdelhamid;
Lenaers, Guy

Publication type:

Article

Characterization of a New BLM Mutation Associated with a Topoisomerase Ilα Defect in a Patient with Bloom's Syndrome.

Published in:

Human Molecular Genetics, 1997, v. 6, n. 9, p. 1427, doi. 10.1093/hmg/6.9.1427

By:

Foucault, Frédéric;
Vaury, Christelle;
Barakat, Abdelhamid;
Thibout, Déborah;
Planchon, Philippe;
Jaulin, Christian;
Praz, Françoise;
Amor-Guéret, Mounira

Publication type:

Article

Novel compound heterozygous MYO7A mutations in Moroccan families with autosomal recessive non-syndromic hearing loss.

Published in:

PLoS ONE, 2017, v. 12, n. 5, p. 1, doi. 10.1371/journal.pone.0176516

By:

Bakhchane, Amina;
Charif, Majida;
Bousfiha, Amale;
Boulouiz, Redouane;
Nahili, Halima;
Rouba, Hassan;
Charoute, Hicham;
Lenaers, Guy;
Barakat, Abdelhamid

Publication type:

Article

c.1643_1644delTG XPC mutation is more frequent in Moroccan patients with xeroderma pigmentosum.

Published in:

Archives of Dermatological Research, 2013, v. 305, n. 1, p. 53, doi. 10.1007/s00403-012-1299-0

By:

Senhaji, Mohamed Amine;
Abidi, Omar;
Nadifi, Sellama;
Benchikhi, Hakima;
Khadir, Khadija;
Ben Rekaya, Mariem;
Eloualid, Abdelmajid;
Messaoud, Olfa;
Abdelhak, Sonia;
Barakat, Abdelhamid

Publication type:

Article

Phylogeography of E1b1b1b-M81 Haplogroup and Analysis of Its Subclades in Morocco.

Published in:

Human Biology, 2014, v. 86, n. 2, p. 105, doi. 10.3378/027.086.0204

By:

Reguig, Ahmed;
Harich, Nourdin;
Barakat, Abdelhamid;
Rouba, Hassan

Publication type:

Article

Y-Chromosome Analysis in Egypt Suggests a Genetic Regional Continuity in Northeastern Africa.

Published in:

Human Biology, 2002, v. 74, n. 5, p. 645, doi. 10.1353/hub.2002.0054

By:

Manni, Franz;
Leonardi, Pascal;
Barakat, Abdelhamid;
Rouba, Hassan;
Heyer, Evelyne;
Klintschar, Michael;
Mcelreavey, Ken;
Quintana-Murci, Lluís

Publication type:

Article

An Unusual Case of Gullo’s Syndrome Concomitant with Serious Endometriosis Disease in a Postmenopausal Woman.

Published in:

2018

By:

Ainahi, Abdelhakim;
Ziane, Abdellaziz;
Wakrim, Lahcen;
Elmdaghri, Naima;
Barakat, Abdelhamid

Publication type:

Case Study

A Novel Homozygous Missense Mutation in the FU-CRD2 Domain of the<bold><italic> R-spondin1 </italic></bold>Gene Associated with Familial 46,XX DSD.

Published in:

Sexual Development, 2017, v. 11, n. 5/6, p. 269, doi. 10.1159/000485393

By:

Naasse, Yassine;
Bakhchane, Amina;
Charoute, Hicham;
Jennane, Farida;
Bignon-Topalovic, Joelle;
Malki, Abderrahim;
Bashamboo, Anu;
Barakat, Abdelhamid;
Rouba, Hassan;
McElreavey, Ken

Publication type:

Article

The Moroccan Genetic Disease Database (MGDD): a database for DNA variations related to inherited disorders and disease susceptibility.

Published in:

European Journal of Human Genetics, 2014, v. 22, n. 3, p. 322, doi. 10.1038/ejhg.2013.151

By:

Charoute, Hicham;
Nahili, Halima;
Abidi, Omar;
Gabi, Khalid;
Rouba, Hassan;
Fakiri, Malika;
Barakat, Abdelhamid

Publication type:

Article

Chromosomal abnormalities and Y chromosome microdeletions in infertile men from Morocco.

Published in:

2015

By:

Naasse, Yassine;
Charoute, Hicham;
El Houate, Brahim;
Elbekkay, Chadli;
Razoki, Lunda;
Malki, Abderrahim;
Barakat, Abdelhamid;
Rouba, Hassan

Publication type:

journal article

Prediction of the Impact of Deleterious Nonsynonymous Single Nucleotide Polymorphisms on the Human RRM2B Gene: A Molecular Modeling Study.

Published in:

BioMed Research International, 2020, p. 1, doi. 10.1155/2020/7614634

By:

Ait El Cadi, Chaimaa;
Krami, Al Mehdi;
Charoute, Hicham;
Elkarhat, Zouhair;
Sifeddine, Najat;
Lakhiari, Hamid;
Rouba, Hassan;
Barakat, Abdelhamid;
Nahili, Halima

Publication type:

Article

Molecular Modelling and Dynamics Study of nsSNP in STXBP1 Gene in Early Infantile Epileptic Encephalopathy Disease.

Published in:

BioMed Research International, 2019, p. 1, doi. 10.1155/2019/4872101

By:

Al Mehdi, Krami;
Fouad, Benhnini;
Zouhair, Elkarhat;
Boutaina, Belkady;
Yassine, Naasse;
Chaimaa, Ait El Cadi;
Najat, Sifeddine;
Hassan, Rouba;
Rachida, Roky;
Abdelhamid, Barakat;
Halima, Nahili

Publication type:

Article

Prediction and Structural Comparison of Deleterious Coding Nonsynonymous Single Nucleotide Polymorphisms (nsSNPs) in Human LEP Gene Associated with Obesity.

Published in:

BioMed Research International, 2019, p. 1, doi. 10.1155/2019/1832084

By:

Bouafi, Hind;
Bencheikh, Sara;
Mehdi Krami, A. L.;
Morjane, Imane;
Charoute, Hicham;
Rouba, Hassan;
Saile, Rachid;
Benhnini, Fouad;
Barakat, Abdelhamid

Publication type:

Article

Association of rs662799 variant and APOA5 gene haplotypes with metabolic syndrome and its components: a meta-analysis in North Africa.

Published in:

Bioscience Reports, 2020, v. 40, n. 8, p. 1, doi. 10.1042/BSR20200706

By:

Hechmi, Meriem;
Dallali, Hamza;
Gharbi, Meriem;
Jmel, Haifa;
Fassatoui, Meriem;
Halima, Yossra Ben;
Bahri, Sonia;
Bahlous, Afaf;
Abid, Abdelmajid;
Jamoussi, Henda;
Barakat, Abdelhamid;
Kefi, Rym

Publication type:

Article

Novel pathogenic WHRN variant causing hearing loss in a moroccan family.

Published in:

Molecular Biology Reports, 2023, v. 50, n. 12, p. 10663, doi. 10.1007/s11033-023-08901-8

By:

AitRaise, Imane;
Amalou, Ghita;
Redouane, Salaheddine;
Charoute, Hicham;
Snoussi, Khalid;
Abdelghaffar, Houria;
Bonnet, Crystel;
Petit, Christine;
Barakat, Abdelhamid

Publication type:

Article

First characterization of congenital myasthenic syndrome type 5 in North Africa.

Published in:

Molecular Biology Reports, 2021, v. 48, n. 10, p. 6999, doi. 10.1007/s11033-021-06530-7

By:

Khaoula, Rochdi;
Cerino, Mathieu;
Da Silva, Nathalie;
Delague, Valerie;
Nahili, Halima;
Kriouile, Yamna;
Gorokhova, Svetlana;
Bartoli, Marc;
Saïle, Rachid;
Barakat, Abdelhamid;
Krahn, Martin

Publication type:

Article

Novel compound heterozygous mutations in the GPR98 ( USH2C) gene identified by whole exome sequencing in a Moroccan deaf family.

Published in:

Molecular Biology Reports, 2017, v. 44, n. 5, p. 429, doi. 10.1007/s11033-017-4129-9

By:

Bousfiha, Amale;
Bakhchane, Amina;
Charoute, Hicham;
Detsouli, Mustapha;
Rouba, Hassan;
Charif, Majida;
Lenaers, Guy;
Barakat, Abdelhamid

Publication type:

Article

TNF A −308G>A polymorphism in Moroccan patients with type 2 diabetes mellitus: a case-control study and meta-analysis.

Published in:

Molecular Biology Reports, 2014, v. 41, n. 9, p. 5805, doi. 10.1007/s11033-014-3454-5

By:

Sefri, Hajar;
Benrahma, Houda;
Charoute, Hicham;
Lakbakbi el yaagoubi, Fouzia;
Rouba, Hassan;
Lyoussi, Badiaa;
Nourlil, Jalal;
Abidi, Omar;
Barakat, Abdelhamid

Publication type:

Article

The c.242G>A mutation in LRTOMT gene is responsible for a high prevalence of deafness in the Moroccan population.

Published in:

Molecular Biology Reports, 2012, v. 39, n. 12, p. 11011, doi. 10.1007/s11033-012-2003-3

By:

Charif, Majida;
Bounaceur, Safaa;
Abidi, Omar;
Nahili, Halima;
Rouba, Hassan;
Kandil, Mostafa;
Boulouiz, Redouane;
Barakat, Abdelhamid

Publication type:

Article

Computational Analysis of nsSNPs of Gene in Severe Combined Immunodeficiency Using Molecular Modeling and Dynamics Simulation.

Published in:

2019

By:

Essadssi, Soukaina;
Krami, Al Mehdi;
Elkhattabi, Lamiae;
Elkarhat, Zouhair;
Amalou, Ghita;
Abdelghaffar, Houria;
Rouba, Hassan;
Barakat, Abdelhamid

Publication type:

journal article

Recessive TBC1D24 Mutations Are Frequent in Moroccan Non-Syndromic Hearing Loss Pedigrees.

Published in:

PLoS ONE, 2015, v. 10, n. 9, p. 1, doi. 10.1371/journal.pone.0138072

By:

Bakhchane, Amina;
Charif, Majida;
Salime, Sara;
Boulouiz, Redouane;
Nahili, Halima;
Roky, Rachida;
Lenaers, Guy;
Barakat, Abdelhamid

Publication type:

Article

Association of APOA5 rs662799 and rs3135506 polymorphisms with arterial hypertension in Moroccan patients.

Published in:

Lipids in Health & Disease, 2014, v. 13, n. 1, p. 60, doi. 10.1186/1476-511X-13-60

By:

Ouatou, Sanaa;
Ajjemami, Maria;
Charoute, Hicham;
Sefri, Hajar;
Ghalim, Noreddine;
Rhaissi, Houria;
Benrahma, Houda;
Barakat, Abdelhamid;
Rouba, Hassan

Publication type:

Article

AZF microdeletions and partial deletions of AZFc region on the Y chromosome in Moroccan men.

Published in:

Asian Journal of Andrology, 2007, v. 9, n. 5, p. 674, doi. 10.1111/j.1745-7262.2007.00290.x

By:

Imken, Laila;
El Houate, Brahim;
Chafik, Abdelaziz;
Nahili, Halima;
Boulouiz, Redouane;
Abidi, Omar;
Chadli, Elbakkay;
Louanjli, Noureddine;
Elfath, Abdelouhab;
Hassar, Mohammed;
McElreavey, Ken;
Barakat, Abdelhamid;
Rouba, Hassan

Publication type:

Article

Novel Mutation in AIFM1 Gene Associated with X-Linked Deafness in a Moroccan Family.

Published in:

Human Heredity, 2020, v. 85, n. 1, p. 35, doi. 10.1159/000512712

By:

Elrharchi, Soukaina;
Riahi, Zied;
Salime, Sara;
Charoute, Hicham;
Elkhattabi, Lamiae;
Boulouiz, Redouane;
Kabine, Mostafa;
Bonnet, Crystel;
Petit, Christine;
Barakat, Abdelhamid

Publication type:

Article

A Homozygous RAG1 Gene Mutation in a Case of Combined Immunodeficiency: Clinical, Molecular, and Computational Analysis.

Published in:

Human Heredity, 2019, v. 84, n. 6, p. 272, doi. 10.1159/000510062

By:

Essadssi, Soukaina;
Benhsaien, Ibtihal;
Bakhchane, Amina;
Charoute, Hicham;
Abdelghaffar, Houria;
Bousfiha, Ahmed Aziz;
Barakat, Abdelhamid

Publication type:

Article

Further Evidence for the Implication of the MET Gene in Non-Syndromic Autosomal Recessive Deafness.

Published in:

Human Heredity, 2019, v. 84, n. 3, p. 109, doi. 10.1159/000503450

By:

Bousfiha, Amale;
Riahi, Zied;
Elkhattabi, Lamiae;
Bakhchane, Amina;
Charoute, Hicham;
Snoussi, Khalid;
Bonnet, Crystel;
Petit, Christine;
Barakat, Abdelhamid

Publication type:

Article

Chromosomal Abnormalities in Patients with Intellectual Disability: A 21-Year Retrospective Study.

Published in:

Human Heredity, 2018, v. 83, n. 5, p. 274, doi. 10.1159/000499710

By:

Belkady, Boutaina;
Elkhattabi, Lamiae;
Elkarhat, Zouhair;
Zarouf, Latifa;
Razoki, Lunda;
Aboulfaraj, Jamila;
Nassereddine, Sanaa;
Cadi, Rachida;
Rouba, Hassan;
Barakat, Abdelhamid

Publication type:

Article

Maternal Effect and Familial Aggregation in a Type 2 Diabetic Moroccan Population.

Published in:

Journal of Community Health, 2011, v. 36, n. 6, p. 943, doi. 10.1007/s10900-011-9393-3

By:

Benrahma, Houda;
Arfa, Imen;
Charif, Majida;
Bounaceur, Safaa;
Eloualid, Abdelmajid;
Boulouiz, Redouane;
Nahili, Halima;
Abidi, Omar;
Rouba, Hassan;
Chadli, Asmaa;
Oudghiri, Mounia;
Farouqui, Ahmed;
Abdelhak, Sonia;
Barakat, Abdelhamid

Publication type:

Article