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Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
April 9, 2013
[Ten practical issues concerning acute poisoning with carbon monoxide in pregnant women]
E Bothuyne-Queste, S Joriot, D Mathieu, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
June 29, 2012
[The consulting physician for withdrawal of life-sustaining treatments in children]
R Cremer, P Fayoux, D Guimber, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
October 3, 2015
[Organization of collaborative deliberation for limiting or withholding treatments in children]
R Cremer, C Lervat, A Laffargue, et al.
Journal of Medical Genetics
|
August 30, 2008
Refinement of cortical dysgeneses spectrum associated with TUBA1A mutations
N Bahi-Buisson, K Poirier, N Boddaert, et al.
Journal of Medical Genetics
|
July 14, 2009
MEF2C haploinsufficiency caused by either microdeletion of the 5q14.3 region or mutation is responsible for severe mental retardation with stereotypic movements, epilepsy and/or cerebral malformations
N Le Meur, M Holder-Espinasse, S Jaillard, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 15) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 15 results.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
April 9, 2013
[Ten practical issues concerning acute poisoning with carbon monoxide in pregnant women]
E Bothuyne-Queste, S Joriot, D Mathieu, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
June 29, 2012
[The consulting physician for withdrawal of life-sustaining treatments in children]
R Cremer, P Fayoux, D Guimber, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
October 3, 2015
[Organization of collaborative deliberation for limiting or withholding treatments in children]
R Cremer, C Lervat, A Laffargue, et al.
Journal of Medical Genetics
|
August 30, 2008
Refinement of cortical dysgeneses spectrum associated with TUBA1A mutations
N Bahi-Buisson, K Poirier, N Boddaert, et al.
Journal of Medical Genetics
|
July 14, 2009
MEF2C haploinsufficiency caused by either microdeletion of the 5q14.3 region or mutation is responsible for severe mental retardation with stereotypic movements, epilepsy and/or cerebral malformations
N Le Meur, M Holder-Espinasse, S Jaillard, et al.
Page
of 2