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Results: 1-6 |
Results: 6

Authors: SMITH M FULLWOOD P QI Y PALMER S UPADHYAYA M COLE T
Citation: M. Smith et al., NO EVIDENCE FOR UNIPARENTAL DISOMY AS A COMMON-CAUSE OF SOTOS SYNDROME, Journal of Medical Genetics, 34(1), 1997, pp. 10-12

Authors: FARNDON P FULLWOOD P HARDY C EVANS G TAYLOR M
Citation: P. Farndon et al., MUTATIONS IN PATCHED AND VARIABLE CLINICAL PHENOTYPES FOUND IN NEVOIDBASAL-CELL CARCINOMA SYNDROME, Journal of Medical Genetics, 34, 1997, pp. 40-40

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

Authors: HARDY C FULLWOOD P FAMDON PA
Citation: C. Hardy et al., A PROTEIN TRUNCATION TEST TO IDENTIFY MUTATIONS IN THE PATCHED (PTCH)GENE IN NEVOID BASAL-CELL CARCINOMA SYNDROME, Journal of Medical Genetics, 34, 1997, pp. 1428-1428

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

Authors: FULLWOOD P BUNDEY S FIELDER AR DUDGEON J KILPATRICK MW
Citation: P. Fullwood et al., X-LINKED EXUDATIVE VITREORETINOPATHY - CLINICAL-FEATURES AND LINKAGE ANALYSIS, Investigative ophthalmology & visual science, 33(4), 1992, pp. 1087-1087
Risultati: 1-6 |