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Results: 1-8 |
Results: 8
IDENTIFICATION OF EXT2 GENE-MUTATIONS IN FAMILIES WITH HEREDITARY MULTIPLE EXOSTOSES
Authors: MITCHELL W RICHARDS FM GATTAS M COLE TRP FARNDON PA
Citation: W. Mitchell et al., IDENTIFICATION OF EXT2 GENE-MUTATIONS IN FAMILIES WITH HEREDITARY MULTIPLE EXOSTOSES, Journal of Medical Genetics, 34, 1997, pp. 61-61
PRENATAL-DIAGNOSIS OF THE NEVOID BASAL-CELL CARCINOMA SYNDROME BY THEIDENTIFICATION OF A MUTATION IN THE PATCHED GENE
Authors: HARDY C FULLWOOD P PETERSEN GB FARNDON PA
Citation: C. Hardy et al., PRENATAL-DIAGNOSIS OF THE NEVOID BASAL-CELL CARCINOMA SYNDROME BY THEIDENTIFICATION OF A MUTATION IN THE PATCHED GENE, Journal of Medical Genetics, 34, 1997, pp. 417-417
GENERAL-PRACTITIONERS EXPECTATIONS OF THE CLINICAL GENETICS SERVICE IN 2 DISTRICTS IN THE WEST MIDLANDS
Authors: FARNDON PA AFFLECK J MOORE J GIBBONS B BINKS A HOWARD J
Citation: Pa. Farndon et al., GENERAL-PRACTITIONERS EXPECTATIONS OF THE CLINICAL GENETICS SERVICE IN 2 DISTRICTS IN THE WEST MIDLANDS, Journal of Medical Genetics, 32(2), 1995, pp. 140-141
ANALYSIS OF 133 MEIOSES PLACES THE GENES FOR NEVOID BASAL-CELL CARCINOMA (GORLIN)-SYNDROME AND FANCONI-ANEMIA GROUP-C IN A 2.6-CM INTERVAL AND CONTRIBUTES TO THE FINE MAP OF 9Q22.3
Authors: FARNDON PA MORRIS DJ HARDY C MCCONVILLE CM WEISSENBACH J KILPATRICK MW REIS A
Citation: Pa. Farndon et al., ANALYSIS OF 133 MEIOSES PLACES THE GENES FOR NEVOID BASAL-CELL CARCINOMA (GORLIN)-SYNDROME AND FANCONI-ANEMIA GROUP-C IN A 2.6-CM INTERVAL AND CONTRIBUTES TO THE FINE MAP OF 9Q22.3, Genomics, 23(2), 1994, pp. 486-489
FLANKING MARKERS FOR THE GORLIN (NEVOID BASAL-CELL CARCINOMA) SYNDROME
Authors: FARNDON PA HARDY C TAYLOR M EVANS DGR KILPATRICK MW
Citation: Pa. Farndon et al., FLANKING MARKERS FOR THE GORLIN (NEVOID BASAL-CELL CARCINOMA) SYNDROME, Cytogenetics and cell genetics, 64(2), 1993, pp. 113-113
EPIDERMAL MOSAICISM AND BLASCHKO LINES
Authors: MOSS C LARKINS S STACEY M BLIGHT A FARNDON PA DAVISON EV
Citation: C. Moss et al., EPIDERMAL MOSAICISM AND BLASCHKO LINES, Journal of Medical Genetics, 30(9), 1993, pp. 752-755
COMPLICATIONS OF THE NEVOID BASAL-CELL CARCINOMA SYNDROME - RESULTS OF A POPULATION-BASED STUDY
Authors: EVANS DGR LADUSANS EJ RIMMER S BURNELL LD THAKKER N FARNDON PA
Citation: Dgr. Evans et al., COMPLICATIONS OF THE NEVOID BASAL-CELL CARCINOMA SYNDROME - RESULTS OF A POPULATION-BASED STUDY, Journal of Medical Genetics, 30(6), 1993, pp. 460-464
GENETIC-MAPPING OF A CONE AND ROD DYSFUNCTION (ALAND ISLAND EYE DISEASE) TO THE PROXIMAL SHORT ARM OF THE HUMAN X-CHROMOSOME
Authors: GLASS IA GOOD P COLEMAN MP FULLWOOD P GILES MG LINDSAY S NEMETH AH DAVIES KE WILLSHAW HA FIELDER A KILPATRICK M FARNDON PA
Citation: Ia. Glass et al., GENETIC-MAPPING OF A CONE AND ROD DYSFUNCTION (ALAND ISLAND EYE DISEASE) TO THE PROXIMAL SHORT ARM OF THE HUMAN X-CHROMOSOME, Journal of Medical Genetics, 30(12), 1993, pp. 1044-1050
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