Published in
Wiley, The American Journal of Medical Genetics - Part A, 4(176), p. 1030-1036, 2018
DOI: 10.1002/ajmg.a.38636
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Biallelic loss-of-function WNT5A mutations in an infant with severe and atypical manifestations of Robinow syndrome
Journal article published in 2018 by
Johannes Birgmeier,
Edward D. Esplin 
,
Karthik A. Jagadeesh,
Harendra Guturu,
Aaron M. Wenger,
Hassan Chaib,
Julia A. Buckingham,
Gill Bejerano ,
Jonathan A. Bernstein
,
Karthik A. Jagadeesh,
Harendra Guturu,
Aaron M. Wenger,
Hassan Chaib,
Julia A. Buckingham,
Gill Bejerano ,
Jonathan A. Bernstein
This paper is made freely available by the publisher.
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