The origin of EFNB1 mutations in craniofrontonasal syndrome%…
The origin of EFNB1 mutations in craniofrontonasal syndrome%2525253A frequent somatic mosaicism and explanation of the paucity of carrier males.
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Elsevier ScienceDirect Journals
Coverage:
- 1997-06~present
Collection:
Cell Press
Coverage:
- 1997-06~present
Collection:
PubMed Central
Coverage:
- 1949~6 months ago