AAAAAA

   
Results: 1-8 |
Results: 8
LOCALIZATION OF THE SCHWARTZ-JAMPEL SYNDROME (SJS) LOCUS TO CHROMOSOME 1P34-P36.1 BY HOMOZYGOSITY MAPPING
Authors: NICOLE S BENHAMIDA C BEIGHTON P BAKOURI S BELAL S ROMERO N VILJOEN D PONSOT G SAMMOUD A WEISSENBACH J FARDEAU M HAMIDA MB FONTAINE B HENTATI F
Citation: S. Nicole et al., LOCALIZATION OF THE SCHWARTZ-JAMPEL SYNDROME (SJS) LOCUS TO CHROMOSOME 1P34-P36.1 BY HOMOZYGOSITY MAPPING, Human molecular genetics, 4(9), 1995, pp. 1633-1636
SUBLOCALIZATION OF AUTOSOMAL RECESSIVE DUCHENNE-LIKE MUSCULAR-DYSTROPHY AND CONSTRUCTION OF A GENETIC-MAP OF CHROMOSOME 13Q12 REGION
Authors: BENOTHMANE K SPEER M CARTER SC BOWCOCK A HAMIDA MB PERICAKVANCE M VANCE JM
Citation: K. Benothmane et al., SUBLOCALIZATION OF AUTOSOMAL RECESSIVE DUCHENNE-LIKE MUSCULAR-DYSTROPHY AND CONSTRUCTION OF A GENETIC-MAP OF CHROMOSOME 13Q12 REGION, Cytogenetics and cell genetics, 70(1-2), 1995, pp. 17-17
LINKAGE OF PURE AUTOSOMAL RECESSIVE FAMILIAL SPASTIC PARAPLEGIA TO CHROMOSOME-8 MARKERS AND EVIDENCE OF GENETIC-LOCUS HETEROGENEITY
Authors: HENTATI A PERICAKVANCE MA HUNG WY BELAL S LAING N BOUSTANY RM HENTATI F HAMIDA MB SIDDIQUE T
Citation: A. Hentati et al., LINKAGE OF PURE AUTOSOMAL RECESSIVE FAMILIAL SPASTIC PARAPLEGIA TO CHROMOSOME-8 MARKERS AND EVIDENCE OF GENETIC-LOCUS HETEROGENEITY, Human molecular genetics, 3(8), 1994, pp. 1263-1267
CD11 CD18 BEARING LYMPHOCYTES IN CEREBROSPINAL-FLUID FROM PATIENTS WITH ACTIVE BEHCETS-DISEASE/
Authors: HAMZAOUI K HAMIDA MB HENTATI F CHABBOU A HAMZAOUI A AYED K KAHAN A
Citation: K. Hamzaoui et al., CD11 CD18 BEARING LYMPHOCYTES IN CEREBROSPINAL-FLUID FROM PATIENTS WITH ACTIVE BEHCETS-DISEASE/, Clinical and experimental rheumatology, 12(5), 1994, pp. 575-576
LINKAGE OF A LOCUS FOR AUTOSOMAL-DOMINANT FAMILIAL SPASTIC PARAPLEGIATO CHROMOSOME 2P MARKERS
Authors: HENTATI A PERICAKVANCE MA LENNON F WASSERMAN B HENTATI F JUNEJA T ANGRIST MH HUNG WY BOUSTANY RM BOHLEGA S IGBAL Z HUETHER CH HAMIDA MB SIDDIQUE T
Citation: A. Hentati et al., LINKAGE OF A LOCUS FOR AUTOSOMAL-DOMINANT FAMILIAL SPASTIC PARAPLEGIATO CHROMOSOME 2P MARKERS, Cytogenetics and cell genetics, 67(4), 1994, pp. 244-244
CLINICAL AND GENETIC-ANALYSIS OF A TUNISIAN FAMILY WITH AUTOSOMAL-DOMINANT CEREBELLAR-ATAXIA TYPE-1 LINKED TO THE SCA2 LOCUS
Authors: BELAL S CANCEL G STEVANIN G HENTATI F KHATI C HAMIDA CB AUBURGER G AGID Y HAMIDA MB BRICE A
Citation: S. Belal et al., CLINICAL AND GENETIC-ANALYSIS OF A TUNISIAN FAMILY WITH AUTOSOMAL-DOMINANT CEREBELLAR-ATAXIA TYPE-1 LINKED TO THE SCA2 LOCUS, Neurology, 44(8), 1994, pp. 1423-1426
GENETIC-LINKAGE ANALYSIS IN 10 TUNISIAN FAMILIES WITH PROGRESSIVE MYOCLONUS EPILEPSY (PME)
Authors: BELAL S HENTATI A AYED M HADDAD M HAMIDA CB FONTAINE B HAMIDA MB HENTATI F
Citation: S. Belal et al., GENETIC-LINKAGE ANALYSIS IN 10 TUNISIAN FAMILIES WITH PROGRESSIVE MYOCLONUS EPILEPSY (PME), Neurology, 44(4), 1994, pp. 10000293-10000294
LINKAGE OF A LOCUS (CMT4A) FOR AUTOSOMAL RECESSIVE CHARCOT-MARIE-TOOTH DISEASE TO CHROMOSOME-8Q
Authors: OTHMANE KB HENTATI F LENNON F HAMIDA CB BLEL S ROSES AD PERICAKVANCE MA HAMIDA MB VANCE JM
Citation: Kb. Othmane et al., LINKAGE OF A LOCUS (CMT4A) FOR AUTOSOMAL RECESSIVE CHARCOT-MARIE-TOOTH DISEASE TO CHROMOSOME-8Q, Human molecular genetics, 2(10), 1993, pp. 1625-1628
Risultati: 1-8 |