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A. Sefiani
Observed names:
A Sefiani,
Abdel Aziz Sefiani,
Aziz Sefiani,
SEFIANI, A.
Institutions:
Mohammed V University,
Institut National d'Hygiène du Maroc,
Centre Hospitalier Ibn Sina
Observed institutions:
Mohammed V University,
Hôpital Necker-Enfants Malades,
National Institutes of Health,
Inserm,
Institut National d'Hygiène du Maroc,
Centre Hospitalier Ibn Sina
show all 6
OpenAlex ID:
A5086152629
A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation
2000
·
Ramzi Zemni
, Thierry Bienvenu
, et al.
·
Nature Genetics
·
244
Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity
1995
·
F. Piccolo
, S.L. Roberds
, et al.
·
Nature Genetics
·
188
The Aurora Kinase C c.144delC mutation causes meiosis I arrest in men and is frequent in the North African population
2009
·
K. Dieterich
, R. Zouari
, et al.
·
Human Molecular Genetics
·
126
The gene for incontinentia pigmenti is assigned to Xq28
1989
·
A. Sefiani
, L. Abel
, et al.
·
Genomics
·
115
Linkage relationship between incontinentia pigmenti (IP2) and nine terminal X long arm markers
1991
·
A. Sefiani
, R. M'rad
, et al.
·
Human Genetics
·
45
Multiple sources of metabolic disturbance inETHE1‐related ethylmalonic encephalopathy
2010
·
Magalie Barth
, Chris Ottolenghi
, et al.
·
Journal of Inherited Metabolic Disease
·
32
Spondyloepiphyseal dysplasia tarda: linkage with genetic markers from the distal short arm of the X chromosome
1988
·
S. Szpiro-Tapia
, A. Sefiani
, et al.
·
Human Genetics
·
32
Linkage studies do not confirm the cytogenetic location of incontinentia pigmenti on Xp11
1988
·
A. Sefiani
, D. Sinnett
, et al.
·
Human Genetics
·
32
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
2011
·
F. El Kerch
, A. Lamzouri
, et al.
·
Journal de gynécologie, obstétrique et biologie de la reproduction. Supplément/Journal de gynécologie obstétrique et biologie de la reproduction
·
25
Genetics and genomic medicine in Morocco: the present hope can make the future bright
2016
·
Khadija Belhassan
, Karim Ouldim
, et al.
·
Molecular Genetics & Genomic Medicine
·
17
PDF
A gene for non-specific X-linked mental retardation (MRX55) is located in Xp11.
1998
·
S C Deqaqi
, M N'Guessan
, et al.
·
PubMed
·
10
Incontinentia pigmenti: Xp breakpoint is not the same in a case of r(X) and in X/autosome translocations.
1989
·
A Sefiani
, S Heuertz
, et al.
·
PubMed
·
10
The first mutations in the MYH gene reported in Moroccan colon cancer patients
2012
·
F.Z. Laarabi
, I. Cherkaoui Jaouad
, et al.
·
Gene
·
8
Omenn Syndrome with Mutation in RAG1 Gene
2008
·
I. Cherkaoui Jaouad
, K. Ouldim
, et al.
·
The Indian Journal of Pediatrics
·
8
Syndrome d’Hutchinson-Gilford (progéria). À propos de 3 cas
2011
·
Y. Doubaj
, A. Lamzouri
, et al.
·
Archives de Pédiatrie
·
5
Incontinentia pigmenti : à propos d’un cas
2007
·
B. Tnacheri Ouazzani
, K. Guedira
, et al.
·
Journal Français d Ophtalmologie
·
2
Autosomal dominant cerebellar ataxia type I in Morocco: presence of the SCA1 and SCA3/MJD mutations
1996
·
A. Benomar
, F. Meggouh
, et al.
·
European Journal of Neurology
·
2
Genetic and allelic heterogeneity of LGMD in North Africa
1997
·
K. Azibi
, M. Chaouch
, et al.
·
Neuromuscular Disorders
·
1
Genetic, allelic and phenotypic heterogeneity of muscular dystrophies with primary and secondary involvement of adhalin (alpha-sarcoglycan)
1996
·
J.-C. Kaplan
, F. Piccolo
, et al.
·
Neuromuscular Disorders
·
1
Diagnostic moléculaire des mutations récurrentes des gènes XPC et XPA chez les patients marocains atteints de xeroderma pigmentosum
2019
·
B. Karrakchou
, I. Ratbi
, et al.
·
Annales de Dermatologie et de Vénéréologie
Intérêt Du Chromosome Philadelphie Dans Les Syndromes Myéloprolifératifs
2013
·
BELKHAYYAT HASSANI, A.
, BENBOUCHTA, Y.
, et al.
·
Maroc médical
Le Retard Mental En Consultation De Genetique
2013
·
CHERKAOUI DEQUAQUI, S.
, BELKHAYYAT, A.
, et al.
·
Maroc médical
Estimation de la prévalence de la mutation p.G352fsdelG du gène PAH de la phénylcétonurie au Maroc
2012
·
F.Z. Laarabi
, A. Lamzouri
, et al.
·
Revue d Épidémiologie et de Santé Publique
Omenn syndrome
2008
·
Imane Cherkaoui Jaouad
, K. Ouldim
, et al.
·
The Indian Journal of Pediatrics
Isolation and characterisation of five new anonymous X-specific probes. One of them detecting a TaqI RFLP.
1993
·
N Belhadj-Kacem
, S Heuertz
, et al.
·
PubMed
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Works count:
26
Citation count:
903
H-index:
10
I10-index:
12
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