Foot Deformities, Congenital/diagnosis/ geneticsRefine your research by the most used items
Author / Editor
- Antonarakis, Stylianos (1)
- Bamshad, M. J. (1)
- Clarkson, K. B. (1)
- Colby, Randall (1)
- Everman, D. B. (1)
- Gurrieri, Fiorella (1)
- Innes, A. M. (1)
- Laughridge, M. E. (1)
- Lyle, Robert (1)
- Morgan, C. T. (1)
Document type
Full text accessibility
Full text version
Subject
- Abnormalities, multiple/diagnosis/ genetics (1)
- Chromosome mapping (1)
- Chromosomes, human, pair 10/ genetics (1)
- Electrophoresis, gel, pulsed-field (1)
- F-box proteins/ genetics (1)
- Foot deformities, congenital/diagnosis/ genetics (1)
- Gene duplication (1)
- Gene frequency (1)
- Gene rearrangement (1)
- Hand deformities, congenital/diagnosis/ genetics (1)
Highlights
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remove all| Title | Authors / Editors | Date | |
|---|---|---|---|
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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 |
