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Leukemia Research
|
April 20, 2023
Effect of single-unit transfusion in patients treated for haematological disease including acute leukemia: A multicenter randomized controlled clinical trial
S P Chantepie, J B Mear, A R Briant, et al.
Annals of Clinical and Translational Neurology
|
March 22, 2018
Placebo-controlled crossover assessment of mecasermin for the treatment of Rett syndrome
Heather M O'Leary, Walter E Kaufmann, Katherine V Barnes, et al.
Clinical Genetics
|
December 25, 2015
A series of 38 novel germline and somatic mutations of NIPBL in Cornelia de Lange syndrome
M Nizon, M Henry, C Michot, et al.
Human Mutation
|
June 15, 2007
Molecular heterogeneity in fetal forms of type II lissencephaly
C Bouchet, M Gonzales, S Vuillaumier-Barrot, et al.
Clinical Genetics
|
March 16, 2013
Molecular characterization of 39 de novo sSMC: contribution to prognosis and genetic counselling, a prospective study
N Marle, D Martinet, A Aboura, et al.
Prenatal Diagnosis
|
January 8, 2014
A French collaborative survey of 272 fetuses with 22q11.2 deletion: ultrasound findings, fetal autopsies and pregnancy outcomes
J Besseau-Ayasse, C Violle-Poirsier, A Bazin, et al.
Page
of 8
Search research articles
Search
Showing results (71-80 of 76) with videos related to
Sort By:
Page
of 8
You have reached the last page of results.
This site can display upto 76 results.
Leukemia Research
|
April 20, 2023
Effect of single-unit transfusion in patients treated for haematological disease including acute leukemia: A multicenter randomized controlled clinical trial
S P Chantepie, J B Mear, A R Briant, et al.
Annals of Clinical and Translational Neurology
|
March 22, 2018
Placebo-controlled crossover assessment of mecasermin for the treatment of Rett syndrome
Heather M O'Leary, Walter E Kaufmann, Katherine V Barnes, et al.
Clinical Genetics
|
December 25, 2015
A series of 38 novel germline and somatic mutations of NIPBL in Cornelia de Lange syndrome
M Nizon, M Henry, C Michot, et al.
Human Mutation
|
June 15, 2007
Molecular heterogeneity in fetal forms of type II lissencephaly
C Bouchet, M Gonzales, S Vuillaumier-Barrot, et al.
Clinical Genetics
|
March 16, 2013
Molecular characterization of 39 de novo sSMC: contribution to prognosis and genetic counselling, a prospective study
N Marle, D Martinet, A Aboura, et al.
Prenatal Diagnosis
|
January 8, 2014
A French collaborative survey of 272 fetuses with 22q11.2 deletion: ultrasound findings, fetal autopsies and pregnancy outcomes
J Besseau-Ayasse, C Violle-Poirsier, A Bazin, et al.
Page
of 8