Published in
Wiley, Birth Defects Research, 6(110), p. 538-542, 2018
DOI: 10.1002/bdr2.1191
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Whole exome sequencing diagnoses the first fetal case of Bainbridge-Ropers syndrome presenting as pontocerebellar hypoplasia type 1
Journal article published in 2018 by
Séverine Bacrot,
Charlotte Mechler,
Naima Talhi,
Dominique Martin-Coignard,
Philippe Roth,
Caroline Michot,
Amale Ichkou,
Olivier Alibeu 
,
Patrick Nitschke,
Sophie Thomas,
Michel Vekemans,
Férechté Razavi,
Lucile Boutaud,
Tania Attie-Bitach
,
Patrick Nitschke,
Sophie Thomas,
Michel Vekemans,
Férechté Razavi,
Lucile Boutaud,
Tania Attie-Bitach
This paper is made freely available by the publisher.
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