Exome sequencing identifies WDR35 variants involved in Sense…
Exome sequencing identifies WDR35 variants involved in Sensenbrenner syndrome.
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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