Authors:
HODES ME
BLANK CA
PRATT VM
MORALES J
NAPIER J
DLOUHY SR
Citation: Me. Hodes et al., NONSENSE MUTATION IN EXON-3 OF THE PROTEOLIPID PROTEIN GENE (PLP) IN A FAMILY WITH AN UNUSUAL FORM OF PELIZAEUS-MERZBACHER-DISEASE, American journal of medical genetics, 69(2), 1997, pp. 121-125
Authors:
PRATT VM
JACKSON CE
WALLACE DC
GURLEY DS
FEIT A
FELDMAN GL
Citation: Vm. Pratt et al., DNA STUDIES OF LIMB-GIRDLE MUSCULAR-DYSTROPHY TYPE 2A IN THE AMISH EXCLUDE A MODIFYING MITOCHONDRIAL GENE AND SHOW NO EVIDENCE FOR A MODIFYING NUCLEAR GENE, American journal of human genetics, 61(1), 1997, pp. 231-233
Authors:
NANCE MA
BOYADJIEV S
PRATT VM
TAYLOR S
HODES ME
DLOUHY SR
Citation: Ma. Nance et al., ADULT-ONSET NEURODEGENERATIVE DISORDER DUE TO PROTEOLIPID PROTEIN GENE MUTATION IN THE MOTHER OF A MAN WITH PELIZAEUS-MERZBACHER DISEASE, Neurology, 47(5), 1996, pp. 1333-1335
Authors:
PRATT VM
BOYADJIEV S
GREEN K
HODES ME
DLOUHY SR
Citation: Vm. Pratt et al., PELIZAEUS-MERZBACHER DISEASE CAUSED BY A DE-NOVO MUTATION THAT ORIGINATED IN EXON-2 OF THE MATERNAL GREAT-GRANDFATHER OF THE PROPOSITUS, American journal of medical genetics, 58(1), 1995, pp. 70-73
Authors:
HODES ME
DEMYER WE
PRATT VM
EDWARDS MK
DLOUHY SR
Citation: Me. Hodes et al., GIRL WITH SIGNS OF PELIZAEUS-MERZBACHER DISEASE HETEROZYGOUS FOR A MUTATION IN EXON-2 OF THE PROTEOLIPID PROTEIN GENE, American journal of medical genetics, 55(4), 1995, pp. 397-401
Authors:
PRATT VM
BOYADJIEV S
DLOUHY SR
SILVER K
DERKALOUSTIAN VM
HODES ME
Citation: Vm. Pratt et al., PELIZAEUS-MERZBACHER-DISEASE IN A FAMILY OF PORTUGUESE ORIGIN CAUSED BY A POINT MUTATION IN EXON-5 OF THE PROTEOLIPID PROTEIN GENE, American journal of medical genetics, 55(4), 1995, pp. 402-404
Authors:
KLEINDORFER DO
DLOUHY SR
PRATT VM
JONES MC
TROFATTER JA
HODES ME
Citation: Do. Kleindorfer et al., IN-FRAME DELETION IN THE PROTEOLIPID PROTEIN GENE OF A FAMILY WITH PELIZAEUS-MERZBACHER DISEASE, American journal of medical genetics, 55(4), 1995, pp. 405-407
Authors:
PRATT VM
NAIDU S
DLOUHY SR
MARKS HG
HODES ME
Citation: Vm. Pratt et al., NOVEL MUTATION IN EXON-3 OF THE PROTEOLIPID PROTEIN GENE IN PELIZAEUS-MERZBACHER-DISEASE, Neurology, 45(2), 1995, pp. 394-395
Citation: Vm. Pratt et al., PELIZAEUS-MERZBACHER-DISEASE - A POINT MUTATION IN EXON-6 OF THE PROTEOLIPID PROTEIN (PLP) GENE, Clinical genetics, 47(2), 1995, pp. 99-100
Authors:
PRATT VM
RICHARD I
BECKMANN JS
JACKSON CE
FELDMAN GL
Citation: Vm. Pratt et al., SEARCH FOR EVIDENCE OF DIGENIC INHERITANCE OF LIMB-GIRDLE MUSCULAR-DYSTROPHY (LGMD2A) IN THE NORTHERN INDIANA AND PENNSYLVANIA AMISH POPULATION, American journal of human genetics, 57(4), 1995, pp. 1974-1974
Citation: Sr. Dlouhy et al., PELIZAEUS-MERZBACHER DISEASE CAUSED BY DENOVO MUTATION, Journal of neuropathology and experimental neurology, 52(3), 1993, pp. 331-331
Authors:
BOYADJIEV S
SAHOTA A
PRATT VM
DLOUHY SR
HODES ME
Citation: S. Boyadjiev et al., DETECTION OF PLP GENE-MUTATIONS IN PATIENTS WITH PELIZAEUS-MERZBACHERDISEASE BY SINGLE-STRAND CONFORMATIONAL-ANALYSIS, American journal of human genetics, 53(3), 1993, pp. 1131-1131
Authors:
KLEINDORFER DO
PRATT VM
TROFATTER JA
DLOUHY SR
HODES ME
Citation: Do. Kleindorfer et al., AN IN-FRAME DELETION IN THE PROTEOLIPID PROTEIN GENE IN A FAMILY WITHPELIZAEUS-MERZBACHER DISEASE, American journal of human genetics, 53(3), 1993, pp. 1171-1171
Authors:
NANCE MA
PRATT VM
BOYADJIEV S
TAYLOR S
HODES ME
DLOUHY SR
Citation: Ma. Nance et al., ADULT-ONSET NEUROLOGICAL DISORDER IN A PELIZAEUS-MERZBACHER DISEASE CARRIER MOTHER, American journal of human genetics, 53(3), 1993, pp. 1745-1745
Authors:
PRATT VM
BOYADJEV S
DLOUHY S
SILVER K
DERKALOUSTIAN V
HODES ME
Citation: Vm. Pratt et al., PELIZAEUS-MERZBACHER DISEASE IN A FAMILY OF PORTUGUESE ORIGIN CAUSED BY A POINT MUTATION IN EXON 5 OF THE PLP GENE, American journal of human genetics, 53(3), 1993, pp. 1751-1751
Authors:
PRATT VM
KIEFER JR
LAHDETIE J
SCHLEUTKER J
HODES ME
DLOUHY SR
Citation: Vm. Pratt et al., LINKAGE OF A NEW MUTATION IN THE PROTEOLIPID PROTEIN (PLP) GENE TO PELIZAEUS-MERZBACHER DISEASE (PMD) IN A LARGE FINNISH KINDRED, American journal of human genetics, 52(6), 1993, pp. 1053-1056