Author:
Moortgat Stephanie,Verellen-Dumoulin Christine,Maystadt Isabelle,Parmentier Benoit,Grisart Bernard,Hennecker Jean-Luc,Destree Anne
Subject
Genetics(clinical),Genetics,General Medicine
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4. Severe feeding problems and congenital laryngostenosis in a patient with 3q23 deletion;Chandler;Eur. J. Pediatr.,1997
5. The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome;Crisponi;Nat. Genet.,2001
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