Concepedia

Publication | Closed Access

Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2

DOI

122

Citations

18

References

1995

Year

Nathaniel H. Robin, George Feldman, Adam Aronson, Heather F. Mitchell, Rosanna Weksberg, Claire O. Leonard, Barbara K. Burton, Kevin D. Josephson, Renata Laxová, Kyrieckos A. Aleck,
Nature Genetics

References

YearCitations

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