REPORT OF THE COMMITTEE-ON-THE-GENETIC-CONSTITUTION-OF-CHROMOSOME-13

[51] MOLECULAR-DETECTION OF DELETIONS INVOLVING BAND Q14 OF CHROMOSOME-13 IN RETINOBLASTOMAS [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (19) : 7391 - 7394

[52] CHROMOSOME-13 RESTRICTION FRAGMENT LENGTH POLYMORPHISMS [J]. HUMAN GENETICS, 1984, 65 (04) : 320 - 324

[53] PARENTAL ORIGIN OF MUTATIONS OF THE RETINOBLASTOMA GENE [J]. NATURE, 1989, 339 (6225) : 556 - 558

[54] HEREDITARY RETINOBLASTOMA AND 13Q-MOSAICISM [J]. CYTOGENETICS AND CELL GENETICS, 1984, 38 (03): : 235 - 237

[55] REEVALUATION OF THE SUBLOCALIZATION OF ESTERASE-D AND ITS RELATION TO THE RETINOBLASTOMA LOCUS BY INSITU HYBRIDIZATION [J]. CYTOGENETICS AND CELL GENETICS, 1987, 44 (2-3): : 153 - 157

[56] IDENTITY OF THE POLYMORPHISMS FOR ESTERASE-D AND S-FORMYLGLUTATHIONE HYDROLASE IN RED-BLOOD-CELLS [J]. HUMAN GENETICS, 1986, 74 (02) : 174 - 175

[57] EMANUEL BS, 1986, AM J HUM GENET, V38, P38

[58] FARRER LA, 1989, CYTOGENET CELL GENET, V51, P997

[59] PREDICTING GENOTYPES AT LOCI FOR AUTOSOMAL RECESSIVE DISORDERS USING LINKED GENETIC-MARKERS - APPLICATION TO WILSONS-DISEASE [J]. HUMAN GENETICS, 1988, 79 (02) : 109 - 117

[60] PREDICTIVE TESTING FOR WILSONS-DISEASE USING TIGHTLY LINKED AND FLANKING DNA MARKERS [J]. NEUROLOGY, 1991, 41 (07) : 992 - 999

[51] MOLECULAR-DETECTION OF DELETIONS INVOLVING BAND Q14 OF CHROMOSOME-13 IN RETINOBLASTOMAS [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (19) : 7391 - 7394

[52] CHROMOSOME-13 RESTRICTION FRAGMENT LENGTH POLYMORPHISMS [J]. HUMAN GENETICS, 1984, 65 (04) : 320 - 324

[53] PARENTAL ORIGIN OF MUTATIONS OF THE RETINOBLASTOMA GENE [J]. NATURE, 1989, 339 (6225) : 556 - 558

[54] HEREDITARY RETINOBLASTOMA AND 13Q-MOSAICISM [J]. CYTOGENETICS AND CELL GENETICS, 1984, 38 (03): : 235 - 237

[55] REEVALUATION OF THE SUBLOCALIZATION OF ESTERASE-D AND ITS RELATION TO THE RETINOBLASTOMA LOCUS BY INSITU HYBRIDIZATION [J]. CYTOGENETICS AND CELL GENETICS, 1987, 44 (2-3): : 153 - 157

[56] IDENTITY OF THE POLYMORPHISMS FOR ESTERASE-D AND S-FORMYLGLUTATHIONE HYDROLASE IN RED-BLOOD-CELLS [J]. HUMAN GENETICS, 1986, 74 (02) : 174 - 175

[57] EMANUEL BS, 1986, AM J HUM GENET, V38, P38

[58] FARRER LA, 1989, CYTOGENET CELL GENET, V51, P997

[59] PREDICTING GENOTYPES AT LOCI FOR AUTOSOMAL RECESSIVE DISORDERS USING LINKED GENETIC-MARKERS - APPLICATION TO WILSONS-DISEASE [J]. HUMAN GENETICS, 1988, 79 (02) : 109 - 117

[60] PREDICTIVE TESTING FOR WILSONS-DISEASE USING TIGHTLY LINKED AND FLANKING DNA MARKERS [J]. NEUROLOGY, 1991, 41 (07) : 992 - 999