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Search Results - Briand, Annaig
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Fryns type mesomelic dysplasia of the upper limbs caused by inverted duplications of the HOXD gene cluster
by
Le Caignec, Cédric
,
Pichon, Olivier
,
Briand, Annaig
,
de Courtivron, Benoît
,
Bonnard, Christian
,
Lindenbaum, Pierre
,
Redon, Richard
,
Schluth-Bolard, Caroline
,
Diguet, Flavie
,
Rollat-Farnier, Pierre-Antoine
,
Sanchez-Castro, Marta
,
Vuillaume, Marie-Laure
,
Sanlaville, Damien
,
Duboule, Denis
,
Mégarbané, André
,
Toutain, Annick
Published in
European journal of human genetics : EJHG
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Autosomal insertional translocation mimicking an X-linked mode of inheritance
by
Thierry, Gaelle
,
Pichon, Olivier
,
Briand, Annaig
,
Poulain, Damien
,
Sznajer, Yves
,
David, Albert
,
Le Caignec, Cédric
Published in
European journal of medical genetics
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Mandibular dysostosis without microphthalmia caused by OTX2 deletion
by
Latypova, Xénia
,
Bordereau, Sylvain
,
Bleriot, Alice
,
Pichon, Olivier
,
Poulain, Damien
,
Briand, Annaïg
,
Le Caignec, Cédric
,
Isidor, Bertrand
Published in
American journal of medical genetics. Part A
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Disruption of the SEMA3D Gene in a Patient with Congenital Heart Defects
by
Sanchez-Castro, Marta
,
Pichon, Olivier
,
Briand, Annaig
,
Poulain, Damien
,
Gournay, Véronique
,
David, Albert
,
Caignec, Cédric Le
Published in
Human mutation
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Wilms' tumor in patients with 9q22.3 microdeletion syndrome suggests a role for PTCH1 in nephroblastomas
by
Isidor, Bertrand
,
Bourdeaut, Franck
,
Lafon, Delfine
,
Plessis, Ghislaine
,
Lacaze, Elodie
,
Kannengiesser, Caroline
,
Rossignol, Sylvie
,
Pichon, Olivier
,
Briand, Annaig
,
Martin-Coignard, Dominique
,
Piccione, Maria
,
David, Albert
,
Delattre, Olivier
,
Jeanpierre, Cécile
,
Sévenet, Nicolas
,
Le Caignec, Cédric
Published in
European journal of human genetics : EJHG
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