Published in
BioMed Central, Molecular Cytogenetics, 1(8), p. 8, 2015
DOI: 10.1186/s13039-015-0107-x
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- BioMed Central | PDF
- [www.ncbi.nlm.nih.gov] | PDF
- [europepmc.org] | PDF
- [www.researchgate.net] | PDF
- [www.ncbi.nlm.nih.gov] | PDF
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Double Xp11.22 deletion including SHROOM4 and CLCN5 associated with severe psychomotor retardation and Dent disease
Journal article published in 2015 by
Narjes Armanet,
Corinne Metay,
Sophie Brisset,
Georges Deschenes,
Dominique Pineau,
François M. Petit 
,
Federico Di Rocco,
Michel Goossens,
Gérard Tachdjian,
Philippe Labrune,
Lucie Tosca
,
Federico Di Rocco,
Michel Goossens,
Gérard Tachdjian,
Philippe Labrune,
Lucie Tosca
This paper is made freely available by the publisher.
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