THE MOLECULAR-BASIS OF HUMAN PIEBALDISM

[1] A NEW ACUTE TRANSFORMING FELINE RETROVIRUS AND RELATIONSHIP OF ITS ONCOGENE V-KIT WITH THE PROTEIN-KINASE GENE FAMILY [J]. NATURE, 1986, 320 (6061) : 415 - 421

[2] ELECTRON MICROSCOPY OF MELANOCYTES IN HUMAN PIEBALDISM [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1965, 45 (01) : 28 - +

[3] FAMILIAL WHITE SKIN SPOTTING (PIEBALDNESS) (PARTIAL ALBINISM) WITH WHITE FORELOCK [J]. JOURNAL OF PEDIATRICS, 1952, 41 (01) : 1 - 12

[4] LOCALIZATION OF THE HUMAN C-KIT PROTOONCOGENE ON THE Q11-Q12 REGION OF CHROMOSOME-4 [J]. HUMAN GENETICS, 1988, 78 (04) : 374 - 376

[5] THE FMS-LIKE TYROSINE KINASE, A RECEPTOR FOR VASCULAR ENDOTHELIAL GROWTH-FACTOR [J]. SCIENCE, 1992, 255 (5047) : 989 - 991

[6] DISTECHE CM, 1989, CYTOGENET CELL GENET, V51, P990

[7] THE KIT LIGAND - A CELL-SURFACE MOLECULE ALTERED IN STEEL MUTANT FIBROBLASTS [J]. CELL, 1990, 63 (01) : 185 - 194

[8] DELETION OF THE C-KIT PROTOONCOGENE IN THE HUMAN DEVELOPMENTAL DEFECT PIEBALD TRAIT [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (23) : 10885 - 10889

[9] FROGGAT P, 1951, IRISH J MED SCI, V398, P86

[10] FUNDERBURK SJ, 1974, AM J HUM GENET, V26, P715

[1] A NEW ACUTE TRANSFORMING FELINE RETROVIRUS AND RELATIONSHIP OF ITS ONCOGENE V-KIT WITH THE PROTEIN-KINASE GENE FAMILY [J]. NATURE, 1986, 320 (6061) : 415 - 421

[2] ELECTRON MICROSCOPY OF MELANOCYTES IN HUMAN PIEBALDISM [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1965, 45 (01) : 28 - +

[3] FAMILIAL WHITE SKIN SPOTTING (PIEBALDNESS) (PARTIAL ALBINISM) WITH WHITE FORELOCK [J]. JOURNAL OF PEDIATRICS, 1952, 41 (01) : 1 - 12

[4] LOCALIZATION OF THE HUMAN C-KIT PROTOONCOGENE ON THE Q11-Q12 REGION OF CHROMOSOME-4 [J]. HUMAN GENETICS, 1988, 78 (04) : 374 - 376

[5] THE FMS-LIKE TYROSINE KINASE, A RECEPTOR FOR VASCULAR ENDOTHELIAL GROWTH-FACTOR [J]. SCIENCE, 1992, 255 (5047) : 989 - 991

[6] DISTECHE CM, 1989, CYTOGENET CELL GENET, V51, P990

[7] THE KIT LIGAND - A CELL-SURFACE MOLECULE ALTERED IN STEEL MUTANT FIBROBLASTS [J]. CELL, 1990, 63 (01) : 185 - 194

[8] DELETION OF THE C-KIT PROTOONCOGENE IN THE HUMAN DEVELOPMENTAL DEFECT PIEBALD TRAIT [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (23) : 10885 - 10889

[9] FROGGAT P, 1951, IRISH J MED SCI, V398, P86

[10] FUNDERBURK SJ, 1974, AM J HUM GENET, V26, P715