COINCIDENCE OF NEUROFIBROMATOSIS AND MYOTONIC-DYSTROPHY IN A KINDRED

[1] FAMILIAL ASSOCIATION OF NEUROFIBROMATOSIS, PERONEAL MUSCULAR-ATROPHY, CONGENITAL DEAFNESS, PARTIAL ALBINISM, AND AXENFELDS DEFECT [J]. BRAIN, 1974, 97 (SEP) : 521 - +

[2] CANALE DJ, 1972, HDB CLIN NEUROLOGY, V14, P147

[3] CROWE EW, 1952, CLIN PATHOLOGICAL GE, P169

[4] HARPER PS, 1972, AM J HUM GENET, V24, P310

[5] HARPER PS, 1979, MYOTONIC DYSTROPHY, P170

[6] HARPER PS, 1979, MYOTONIC DYSTROPHY, P32

[7] HARPER PS, 1979, MYOTONIC DYSTROPHY, P227

[8] KISSEL P, 1954, REV NEUROL, V91, P299

[9] MONTEL M, 1925, ARCH MED PHARM MILIT, V83, P77

[10] MORTON NE, 1956, AM J HUM GENET, V8, P80

[1] FAMILIAL ASSOCIATION OF NEUROFIBROMATOSIS, PERONEAL MUSCULAR-ATROPHY, CONGENITAL DEAFNESS, PARTIAL ALBINISM, AND AXENFELDS DEFECT [J]. BRAIN, 1974, 97 (SEP) : 521 - +

[2] CANALE DJ, 1972, HDB CLIN NEUROLOGY, V14, P147

[3] CROWE EW, 1952, CLIN PATHOLOGICAL GE, P169

[4] HARPER PS, 1972, AM J HUM GENET, V24, P310

[5] HARPER PS, 1979, MYOTONIC DYSTROPHY, P170

[6] HARPER PS, 1979, MYOTONIC DYSTROPHY, P32

[7] HARPER PS, 1979, MYOTONIC DYSTROPHY, P227

[8] KISSEL P, 1954, REV NEUROL, V91, P299

[9] MONTEL M, 1925, ARCH MED PHARM MILIT, V83, P77

[10] MORTON NE, 1956, AM J HUM GENET, V8, P80