Downloads provided by UsageCounts
doi: 10.1002/ajmg.10779
pmid: 12357471
AbstractDisorders that include polydactyly as a manifestation are diverse and numerous. Cataloging these disorders by phenotype and genotype demonstrates numerous overlapping phenotypes, genetic heterogeneity of phenotypes, and distinct phenotypes generated from mutations in single genes. To assess these issues, a list of disorders with polydactyly has been compiled from several sources. Among 119 disorders, 39 disorders are associated with mutations in genes, and among these, genotypic and phenotypic overlap is demonstrated. These issues highlight the need for a diagnostic system that catalogs both genotype and phenotype. Published 2002 Wiley‐Liss, Inc.
Polydactyly, Phenotype, Genotype, Mutation, Chromosome Mapping, Humans, Abnormalities, Multiple, Syndrome
Polydactyly, Phenotype, Genotype, Mutation, Chromosome Mapping, Humans, Abnormalities, Multiple, Syndrome
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 51 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 10% | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |
| views | 87 | |
| downloads | 38 |

Views provided by UsageCounts
Downloads provided by UsageCounts