Authors:
VANCE JM
DENTON PH
MIDDLETON L
LOEB D
LENNON F
STAJICH JM
WOLPERT C
PERICAKVANCE MA
Citation: Jm. Vance et al., EXAMINATION OF THE PREVALENCE OF CHARCOT-MARIE-TOOTH-TYPE 2A AND REFINED MAPPING OF THE 1P36 LOCUS, Neurology, 46(2), 1996, pp. 2011-2011
Authors:
BENOTHMANE K
LOEB D
HAYWORTHHODGTE R
HENTATI F
RAO N
ROSES AD
BENHAMIDA M
PERICAKVANCE MA
VANCE JM
Citation: K. Benothmane et al., PHYSICAL AND GENETIC-MAPPING OF THE CMT4A LOCUS AND EXCLUSION OF PMP-2 AS THE DEFECT IN CMT4A, Genomics, 28(2), 1995, pp. 286-290
Authors:
BENOTHMANE K
LOEB D
RAO N
HAYWORTHHOTGE R
ROSES AD
PERICAKVANCE MA
BENHAMIDA M
VANCE JM
Citation: K. Benothmane et al., GENETIC AND PHYSICAL MAPPING OF THE GENOMIC REGION SPANNING CMT4A, Cytogenetics and cell genetics, 68(3-4), 1995, pp. 156-156
Citation: D. Loeb, SYMPHONIC UNITY - THE DEVELOPMENT OF FORMAL THINKING IN THE SYMPHONIES OF SIBELIUS - MURTOMAKI,V, Music theory spectrum, 17(1), 1995, pp. 124-128
Authors:
BENOTHMANE K
SPEER M
MIDDLETON LT
LOEB D
HENTATI F
BENHAMIDA M
PERICAKVANCE MA
VANCE JM
Citation: K. Benothmane et al., LINKAGE DISEQUILIBRIUM IN THE DUCHENNE-LIKE MUSCULAR-DYSTROPHY NDLMD)REGION REFINES THE LOCALIZATION OF THE DISEASE GENE TO LESS-THAN U CM, Neurology, 45(4), 1995, pp. 243-243
Authors:
BENOTHMANE K
DENTON P
SPEER MC
STAUFFER J
LOEB D
RAO N
MIDDLETON ML
BENHAMIDA M
PERICAKVANCE MA
VANCE JM
Citation: K. Benothmane et al., LIMB-GIRDLE MUSCULAR-DYSTROPHY TYPE 2C (LGMD2C) - IDENTIFICATION OF LINKAGE DISEQUILIBRIUM AND INITIATION OF A PHYSICAL MAP SPANNING THE REGION, American journal of human genetics, 57(4), 1995, pp. 1071-1071
Authors:
BENOTHMANE K
SPEER MC
STAUFFER J
BLEL S
MIDDLETON L
BENHAMIDA C
ETRIBI A
LOEB D
HENTATI F
ROSES AD
BENHAMIDA M
PERICAKVANCE MA
VANCE JM
Citation: K. Benothmane et al., EVIDENCE FOR LINKAGE DISEQUILIBRIUM IN CHROMOSOME 13-LINKED DUCHENNE-LIKE MUSCULAR-DYSTROPHY (LGMD2C), American journal of human genetics, 57(3), 1995, pp. 732-734
Authors:
DENTON PH
CULLEN JB
LOEB D
LUCAS A
NUNES K
HULETT C
VANCE JM
Citation: Ph. Denton et al., PARTITIONED PULSED-FIELD GEL ELECTROPHORESIS-PCR (PPF-PCR) - A NEW METHOD FOR PULSED-FIELD MAPPING FOR STS AND MICROSATELLITES, Nucleic acids research, 22(9), 1994, pp. 1776-1777
Authors:
DENTON P
RAO N
PETTENATI MJ
LOEB D
DENG HX
LENNON F
BENOTHMANE K
SIDDIQUE T
PERICAKVANCE MA
VANCE JM
Citation: P. Denton et al., MAPPING OF THE CHROMOSOME 1P36 REGION SURROUNDING THE CHARCOT-MARIE-TOOTH DISEASE TYPE 2A LOCUS, Cytogenetics and cell genetics, 67(3), 1994, pp. 167-167
Authors:
BENOTHMANE K
HENTATI F
LENNON F
BENHAMIDA C
BLEL S
LOEB D
RAO N
ROSES AD
PERICAKVANCE MA
BENHAMIDA M
VANCE JM
Citation: K. Benothmane et al., AUTOSOMAL RECESSIVE CHARCOT-MARIE-TOOTH DISEASE - CLASSIFICATION AND GENETIC-LINKAGE OF ONE FORM (CMT4A) TO CHROMOSOME 8Q, Neurology, 44(4), 1994, pp. 10000361-10000361
Citation: D. Loeb et al., DINUCLEOTIDE REPEAT POLYMORPHISMS IN THE VHL REGION OF HUMAN CHROMOSOME-3P25, Human molecular genetics, 2(10), 1993, pp. 1746-1746
Authors:
VANCE JM
LOEB D
NUNES K
LIU W
RIMMLER J
STAJICH J
SMITH DI
PERICAKVANCE MA
Citation: Jm. Vance et al., GENETIC-MAPPING OF MICROSATELLITES IN THE 3P25 REGION OF VONHIPPEL-LINDAU DISEASE (VHL), Neurology, 43(4), 1993, pp. 358-358
Authors:
BENOTHMANE K
BENHAMIDA M
LENNON F
LOEB D
HENTATI F
BENHAMIDA C
BLEL S
PERICAKVANCE MA
VANCE JM
Citation: K. Benothmane et al., AUTOSOMAL RECESSIVE CHARCOT-MARIE-TOOTH DISEASE (CMT4) TYPE-A - EVIDENCE OF GENETIC-LINKAGE TO CHROMOSOME-8Q21, American journal of human genetics, 53(3), 1993, pp. 149-149
Authors:
LOEB D
BENOTHMANE K
BENHAMIDA C
SPEER M
CARTER S
BOWCOCK AM
BLEL S
HENTATI F
ROSES AD
BENHAMIDA M
PERICAKVANCE MA
VANCE JM
Citation: D. Loeb et al., SUBLOCALIZATION OF AUTOSOMAL RECESSIVE DUCHENNE-LIKE MUSCULAR-DYSTROPHY (DLMD) TO A 5 CM REGION OF 13Q12, American journal of human genetics, 53(3), 1993, pp. 1038-1038
Authors:
DENTON PH
CULLEN B
LOEB D
NUNES K
VANCE JM
Citation: Ph. Denton et al., PARTITIONED PULSED-FIELD GEL ELECTROPHORESIS-PCR (PPF-PCR) - A NEW METHOD FOR PULSED-FIELD MAPPING FOR STS AND MICROSATELLITES, American journal of human genetics, 53(3), 1993, pp. 1283-1283