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Archives de pédiatrie
Volume 20, n° 4
page 425 (avril 2013)
Doi : 10.1016/j.arcped.2013.01.034

Syndrome de Börjeson-Forssman-Lehmann : phénotype et évolution clinique de la cohorte française

I. Marey a, , F. Prieur b, S. Blesson c, P. Edery d, J. Roume e, R. Touraine b, V. Des Portes f, D. Héron a
a Service de génétique médicale, hôpital Pitié Salpêtrière, Paris, France 
b Service de génétique médicale, CHU Saint-Étienne, Saint-Étienne, France 
c Service de génétique médicale, CHU Tours, Tours, France 
d Service de génétique médicale, CHU Lyon, Lyon, France 
e Service de génétique médicale, CHI de Poissy, Poissy, France 
f Service de neuropédiatrie, CHU Lyon, Lyon, France 

Auteur correspondant.

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