F-Box Proteins/ geneticsRefine your research by the most used items
Author / Editor
- Antonarakis, Stylianos (2)
- Everman, D. B. (2)
- Gurrieri, Fiorella (2)
- Lyle, Robert (2)
- Schwartz, C. E. (2)
- Bamshad, M. J. (1)
- Blouin, Jean-Louis (1)
- Clarkson, K. B. (1)
- Colby, Randall (1)
- Delozier-Blanchet, Celia (1)
Document type
Full text accessibility
Full text version
Subject
- Chromosomes, human, pair 10/ genetics (2)
- F-box proteins/ genetics (2)
- Gene duplication (2)
- Humans (2)
- Abnormalities, multiple/diagnosis/ genetics (1)
- Beta-transducin repeat-containing proteins/genetics (1)
- Chromosome mapping (1)
- Electrophoresis, gel, pulsed-field (1)
- Female (1)
- Foot deformities, congenital/diagnosis/ genetics (1)
Highlights
Show items per page
remove all| Title | Authors / Editors | Date | |
|---|---|---|---|
 |
Frequency of genomic rearrangements involving the SHFM3 locus at chromosome 10q24 in syndromic and non-syndromic split-hand/foot malformation | Everman, D. B.; Morgan, C. T.; Lyle, Robert; Laughridge, M. E.; ... Schwartz, C. E. | 2006 |
|
|
Split-hand/split-foot malformation 3 (SHFM3) at 10q24, development of rapid diagnostic methods and gene expression from the region | Lyle, Robert; Radhakrishna, Uppala; Blouin, Jean-Louis; Gagos, Sarantis; ... Antonarakis, Stylianos | 2006 |
