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Showing results (41-50 of 45) with videos related to

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 29, 2012
[Epidemiology of orofacial clefts (1995-2006) in France (Congenital Malformations of Alsace Registry)]B Doray, D Badila-Timbolschi, E Schaefer, et al.
Prenatal Diagnosis|June 26, 2014
Pregnancy outcomes of prenatally diagnosed Turner syndrome: a French multicenter retrospective study including a series of 975 casesN Gruchy, F Vialard, E Blondeel, et al.
Journal of Medical Genetics|June 5, 2010
Microdeletion at chromosome 4q21 defines a new emerging syndrome with marked growth restriction, mental retardation and absent or severely delayed speechC Bonnet, J Andrieux, M Béri-Dexheimer, et al.
Clinical Genetics|March 19, 2010
Delineation of 15q13.3 microdeletionsA Masurel-Paulet, J Andrieux, P Callier, et al.
Clinical Genetics|March 16, 2013
Molecular characterization of 39 de novo sSMC: contribution to prognosis and genetic counselling, a prospective studyN Marle, D Martinet, A Aboura, et al.
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Showing results (41-50 of 45) with videos related to

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Pageof 5
You have reached the last page of results.This site can display upto 45 results.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 29, 2012
[Epidemiology of orofacial clefts (1995-2006) in France (Congenital Malformations of Alsace Registry)]B Doray, D Badila-Timbolschi, E Schaefer, et al.
Prenatal Diagnosis|June 26, 2014
Pregnancy outcomes of prenatally diagnosed Turner syndrome: a French multicenter retrospective study including a series of 975 casesN Gruchy, F Vialard, E Blondeel, et al.
Journal of Medical Genetics|June 5, 2010
Microdeletion at chromosome 4q21 defines a new emerging syndrome with marked growth restriction, mental retardation and absent or severely delayed speechC Bonnet, J Andrieux, M Béri-Dexheimer, et al.
Clinical Genetics|March 19, 2010
Delineation of 15q13.3 microdeletionsA Masurel-Paulet, J Andrieux, P Callier, et al.
Clinical Genetics|March 16, 2013
Molecular characterization of 39 de novo sSMC: contribution to prognosis and genetic counselling, a prospective studyN Marle, D Martinet, A Aboura, et al.
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