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Clinical interest of molecular study in cases of isolated midline craniosynostosis
by
Di Rocco, Federico
,
Rossi, Massimiliano
,
Verlut, Isabelle
,
Szathmari, Alexandru
,
Beuriat, Pierre Aurélien
,
Chatron, Nicolas
,
Chauvel-Picard, Julie
,
Mottolese, Carmine
,
Monin, Pauline
,
Vinchon, Matthieu
,
Guernouche, Sofia
,
Collet, Corinne
Published in
European journal of human genetics : EJHG
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European Journal Of Human Genetics : Ejhg
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Biochemistry & Molecular Biology
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Birth Defects
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Child
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Child, Preschool
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Cranial Sutures
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Craniosynostoses - Diagnosis
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Craniosynostoses - Genetics
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Craniosynostosis
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Dysostosis
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Fibroblast Growth Factor Receptor 2
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Genetics & Heredity
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Humans
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Infants
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