Two Indian families with Greig cephalopolysyndactyly with non-syndromic phenotype

Authors

Keywords

Greig cephalopolysyndactyly syndrome, <em class=EmphasisTypeItalic >GL13</em> mutation, Hypertelorism, Macrocephaly, Polysyndactyly

Journal

Volume 172, Issue 8, Pages 1131-1135

Publisher

Springer Nature

Online

2013-01-18

DOI

10.1007/s00431-013-1938-2

References

View 4 related references

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