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Results: 1-8 |
Results: 8
AUTOSOMAL RECESSIVE ANHIDROTIC ECTODERMAL DYSPLASIA IN A LARGE MOROCCAN FAMILY
Authors: KABBAJ K BAALA L CHHOUL H SEFIANI A
Citation: K. Kabbaj et al., AUTOSOMAL RECESSIVE ANHIDROTIC ECTODERMAL DYSPLASIA IN A LARGE MOROCCAN FAMILY, Journal of Medical Genetics, 35(12), 1998, pp. 1043-1044
A GENE FOR NONSPECIFIC X-LINKED MENTAL-RETARDATION (MRX55) IS LOCATEDIN XP11
Authors: DEQAQI SC NGUESSAN M FORNER J SBITI A BELDJORD C CHELLY J SEFIANI A DESPORTES V
Citation: Sc. Deqaqi et al., A GENE FOR NONSPECIFIC X-LINKED MENTAL-RETARDATION (MRX55) IS LOCATEDIN XP11, Annales de genetique, 41(1), 1998, pp. 11-16
AUTOSOMAL-DOMINANT CEREBELLAR-ATAXIA TYPE-I IN MOROCCO - PRESENCE OF THE SCAI AND SCA3 MJD MUTATIONS/
Authors: BENOMAR A MEGGOUH F DIDIERJEAN O KISSANI N DURR A SEFIANI A CHKILI T AGID Y YAHYAOUI M BRICE A
Citation: A. Benomar et al., AUTOSOMAL-DOMINANT CEREBELLAR-ATAXIA TYPE-I IN MOROCCO - PRESENCE OF THE SCAI AND SCA3 MJD MUTATIONS/, European journal of neurology, 3(4), 1996, pp. 369-372
ADHALIN-DEFICIENT MUSCULAR-DYSTROPHIES - CLINICAL, PATHOLOGICAL, AND GENETIC CORRELATIONS
Authors: EYMARD B ROMERO NB LETURCQ F CARRIE A PICCOLO F COLLIN H KAPLAN JC TOME FMS FARDEAU M AZIBI K CHAOUCH M MERLINI L PENISSON I SEFIANI A CAMPBELL KP
Citation: B. Eymard et al., ADHALIN-DEFICIENT MUSCULAR-DYSTROPHIES - CLINICAL, PATHOLOGICAL, AND GENETIC CORRELATIONS, Neurology, 46(2), 1996, pp. 68006-68006
APOLIPOPROTEIN-E GENOTYPING IN SPORADIC AMYOTROPHIC-LATERAL-SCLEROSIS- EVIDENCE FOR A MAJOR INFLUENCE ON THE CLINICAL PRESENTATION AND PROGNOSIS
Authors: MOULARD B SEFIANI A LAAMRI A MALAFOSSE A CAMU W
Citation: B. Moulard et al., APOLIPOPROTEIN-E GENOTYPING IN SPORADIC AMYOTROPHIC-LATERAL-SCLEROSIS- EVIDENCE FOR A MAJOR INFLUENCE ON THE CLINICAL PRESENTATION AND PROGNOSIS, Journal of the neurological sciences, 139, 1996, pp. 34-37
PRIMARY ADHALINOPATHY - A COMMON-CAUSE OF AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY OF VARIABLE SEVERITY
Authors: PICCOLO F ROBERDS SL JEANPIERRE M LETURCQ F AZIBI K BELDJORD C CARRIE A RECAN D CHAOUCH M REGHIS A ELKERCH F SEFIANI A VOIT T MERLINI L COLLIN H EYMARD B BECKMANN JS ROMERO NB TOME FMS FARDEAU M CAMPBELL KP KAPLAN JC
Citation: F. Piccolo et al., PRIMARY ADHALINOPATHY - A COMMON-CAUSE OF AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY OF VARIABLE SEVERITY, Nature genetics, 10(2), 1995, pp. 243-245
LINKAGE ANALYSIS OF FAMILIES WITH SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY IN MOROCCO INDICATES GENETIC HOMOGENEITY OF THE DISEASE IN NORTH-AFRICA
Authors: ELKERCH F SEFIANI A AZIBI K BOUTALEB N YAHYAOUI M BENTAHILA A VINET MC LETURCQ F BACHNER L BECKMANN J CAMPBELL KP TOME FMS FARDEAU M KAPLAN JC
Citation: F. Elkerch et al., LINKAGE ANALYSIS OF FAMILIES WITH SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY IN MOROCCO INDICATES GENETIC HOMOGENEITY OF THE DISEASE IN NORTH-AFRICA, Journal of Medical Genetics, 31(4), 1994, pp. 342-343
ISOLATION AND CHARACTERIZATION OF 5 NEW ANONYMOUS X-SPECIFIC PROBES -ONE OF THEM DETECTING A TAQI RFLP
Authors: BELHADJKACEM N HEUERTZ S HORSCAYLA MC SAIDIMEHTAR N SEFIANI A
Citation: N. Belhadjkacem et al., ISOLATION AND CHARACTERIZATION OF 5 NEW ANONYMOUS X-SPECIFIC PROBES -ONE OF THEM DETECTING A TAQI RFLP, Annales de genetique, 36(3), 1993, pp. 139-143
Risultati: 1-8 |