Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by
Crossref.
Laarabi, F
Jaouad, I
El Kerch, F
and
Sefiani, A
2009.
MYH Associated Polyposis with a p.Tyr165Cys Mutation in a Moroccan Patient.
Balkan Journal of Medical Genetics,
Vol. 12,
Issue. 2,
p.
65.
Sefiani, Abdelaziz
2010.
Genetic Disorders Among Arab Populations.
p.
455.
Borhany, Munira
Pahore, Zaen
ul Qadr, Zeeshan
Rehan, Muhammad
Naz, Arshi
Khan, Asif
Ansari, Saqib
Farzana, Tasneem
Nadeem, Muhammad
Raza, Syed Amir
and
Shamsi, Tahir
2010.
Bleeding disorders in the tribe: result of consanguineous in breeding.
Orphanet Journal of Rare Diseases,
Vol. 5,
Issue. 1,
Wahabi, Hayfaa A
Alzeidan, Rasmeia A
Bawazeer, Ghada A
Alansari, Lubna A
and
Esmaeil, Samia A
2010.
Preconception care for diabetic women for improving maternal and fetal outcomes: a systematic review and meta-analysis.
BMC Pregnancy and Childbirth,
Vol. 10,
Issue. 1,
Sbiti, A.
Ratbi, I.
Kriouile, Y.
and
Sefiani, A.
2011.
L’amyotrophie spinale infantile : cause fréquente des hypotonies congénitales au Maroc.
Archives de Pédiatrie,
Vol. 18,
Issue. 12,
p.
1261.
AL-KANDARI, YAGOUB Y.
and
CREWS, DOUGLAS E.
2011.
THE EFFECT OF CONSANGUINITY ON CONGENITAL DISABILITIES IN THE KUWAITI POPULATION.
Journal of Biosocial Science,
Vol. 43,
Issue. 1,
p.
65.
Laarabi, F. Z.
Cherkaoui Jaouad, I.
Benazzouz, A.
Squalli, D.
and
Sefiani, A.
2011.
Prevalence of MYH-associated polyposis related to three recurrent mutations in Morocco.
Annals of Human Biology,
Vol. 38,
Issue. 3,
p.
360.
Shawky, Rabah M.
and
Sadik, Doaa I.
2011.
Congenital malformations prevalent among Egyptian children and associated risk factors.
Egyptian Journal of Medical Human Genetics,
Vol. 12,
Issue. 1,
p.
69.
El Kerch, F.
Lamzouri, A.
Laarabi, F.Z.
Zahi, M.
Ben Amar, B.
and
Sefiani, A.
2011.
Confirmation de la forte prévalence au Maroc de la mutation homozygote c.144delC du gène aurora kinase C (AURKC) dans les tératozoospermies avec spermatozoïdes macrocéphales.
Journal de Gynécologie Obstétrique et Biologie de la Reproduction,
Vol. 40,
Issue. 4,
p.
329.
la Marca, Giancarlo
Malvagia, Sabrina
Pasquini, Elisabetta
Cavicchi, Catia
Morrone, Amelia
Ciani, Federica
Funghini, Silvia
Villanelli, Fabio
Zammarchi, Enrico
and
Guerrini, Renzo
2011.
JIMD Reports - Case and Research Reports, 2011/1.
Vol. 1,
Issue. ,
p.
107.
Cauchi, S.
Ezzidi, I.
El Achhab, Y.
Mtiraoui, N.
Chaieb, L.
Salah, D.
Nejjari, C.
Labrune, Y.
Yengo, L.
Beury, D.
Vaxillaire, M.
Mahjoub, T.
Chikri, M.
and
Froguel, P.
2012.
European genetic variants associated with type 2 diabetes in North African Arabs.
Diabetes & Metabolism,
Vol. 38,
Issue. 4,
p.
316.
Wahabi, Hayfaa A
Alzeidan, Rasmieh A
and
Esmaeil, Samia A
2012.
Pre-pregnancy care for women with pre-gestational diabetes mellitus: a systematic review and meta-analysis.
BMC Public Health,
Vol. 12,
Issue. 1,
Tajir, Mariam
Arnoux, Jean Baptiste
Boutron, Audrey
Elalaoui, Siham Chafai
De Lonlay, Pascale
Sefiani, Abdelaziz
and
Brivet, Michèle
2012.
Pyruvate dehydrogenase deficiency caused by a new mutation of PDHX gene in two Moroccan patients.
European Journal of Medical Genetics,
Vol. 55,
Issue. 10,
p.
535.
Lamzouri, Afaf
Ratbi, Ilham
Laarabi, Fatima Z.
Barkat, Amina
and
Sefiani, Abdelaziz
2012.
Low Prevalence of p.G352fsdelG Mutation in Phenylketonuria Patients from Morocco.
Genetic Testing and Molecular Biomarkers,
Vol. 16,
Issue. 8,
p.
996.
Laarabi, F.Z.
Cherkaoui Jaouad, I.
Baert-Desurmont, S.
Ouldim, K.
Ibrahimi, A.
Kanouni, N.
Frebourg, T.
and
Sefiani, A.
2012.
The first mutations in the MYH gene reported in Moroccan colon cancer patients.
Gene,
Vol. 496,
Issue. 1,
p.
55.
Lyahyai, Jaber
Sbiti, Aziza
Barkat, Amina
Ratbi, Ilham
and
Sefiani, Abdelaziz
2012.
Spinal Muscular Atrophy Carrier Frequency and Estimated Prevalence of the Disease in Moroccan Newborns.
Genetic Testing and Molecular Biomarkers,
Vol. 16,
Issue. 3,
p.
215.
Hama, I.
Ratbi, I.
Reggoug, S.
Elkerch, F.
Kharrasse, G.
Errabih, I.
Ouazzani, H.
and
Sefiani, A.
2012.
Non-association of Crohn's disease with NOD2 gene variants in Moroccan patients.
Gene,
Vol. 499,
Issue. 1,
p.
121.
DOUBAJ, Yassamine
LAARABI, Fatima‐Zahra
CHAFAI ELALAOUI, Siham
BARKAT, Amina
and
SEFIANI, Abdelaziz
2012.
Carrier frequency of the recurrent mutation c.1643_1644delTG in the XPC gene and birth prevalence of the xeroderma pigmentosum in Morocco.
The Journal of Dermatology,
Vol. 39,
Issue. 4,
p.
382.
Weller, Mathias
Tanieri, Marina
Pereira, Josecleide Calixto
Almeida, Ednno Dos Santos
Kok, Fernando
and
Santos, Silvana
2012.
Consanguineous unions and the burden of disability: A population‐based study in communities of Northeastern Brazil.
American Journal of Human Biology,
Vol. 24,
Issue. 6,
p.
835.
Assady, Suheir
Ramadan, Rawi
and
Rubinger, Dvora
2012.
Brenner and Rector's The Kidney.
p.
2744.