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American Journal of Medical Genetics
|
January 25, 2002
Osteopathia striata cranial sclerosis: non-random X-inactivation suggestive of X-linked dominant inheritance
Géraldine Viot, Didier Lacombe, Albert David, et al.
Cancer Epidemiology
|
August 20, 2011
Investigating the completeness of a histopathological cancer registry: estimation by capture-recapture analysis in a French geographical unit Alpes-Maritimes, 2008
Laurent Bailly, Bernard Giusiano, Eugènia Mariné Barjoan, et al.
American Journal of Medical Genetics. Part A
|
September 27, 2014
Inverted duplication with deletion: first interstitial case suggesting a novel undescribed mechanism of formation
J Milosevic, L El Khattabi, A Roubergue, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences
|
November 4, 2019
Role of P-glycoprotein in the brain disposition of seletalisib: Evaluation of the potential for drug-drug interactions
Jean-Marie Nicolas, Hugues Chanteux, Johan Nicolaï, et al.
Applied Radiation and Isotopes : Including Data, Instrumentation and Methods for Use in Agriculture, Industry and Medicine
|
March 28, 2015
Development of a freeze-dried kit formulation for the preparation of 99mTc-NTP 15-5, a radiotracer for scintigraphic imaging of proteoglycans
Aurélien Vidal, Vincent Gaumet, Marie-Josèphe Galmier, et al.
Prenatal Diagnosis
|
March 12, 1999
Prenatal detection of a 1p36 deletion in a fetus with multiple malformations and a review of the literature
L Faivre, N Morichon-Delvallez, G Viot, et al.
Journal of Medical Genetics
|
October 4, 2002
Homozygosity mapping of a Dyggve-Melchior-Clausen syndrome gene to chromosome 18q21.1
C Thauvin-Robinet, V El Ghouzzi, W Chemaitilly, et al.
Gynecologie, Obstetrique, Fertilite & Senologie
|
February 15, 2020
[Adverse obstetric and perinatal outcome with in vitro fertilization technology: A French nationwide population-based study]
F Pessione, J De Mouzon, A Deveaux, et al.
Reproductive Biomedicine Online
|
March 3, 2023
Risk factors associated with preterm birth in singletons born after IVF: a national cohort study
Marie-Josée Gervoise-Boyer, Patricia Fauque, Jacques De Mouzon, et al.
European Journal of Radiology
|
December 17, 2013
CMR assessment after a transapical-transcatheter aortic valve implantation
Loïc Biere, Frédéric Pinaud, Stéphane Delépine, et al.
Page
of 23
Search research articles
Search
Showing results (161-170 of 228) with videos related to
Sort By:
Page
of 23
American Journal of Medical Genetics
|
January 25, 2002
Osteopathia striata cranial sclerosis: non-random X-inactivation suggestive of X-linked dominant inheritance
Géraldine Viot, Didier Lacombe, Albert David, et al.
Cancer Epidemiology
|
August 20, 2011
Investigating the completeness of a histopathological cancer registry: estimation by capture-recapture analysis in a French geographical unit Alpes-Maritimes, 2008
Laurent Bailly, Bernard Giusiano, Eugènia Mariné Barjoan, et al.
American Journal of Medical Genetics. Part A
|
September 27, 2014
Inverted duplication with deletion: first interstitial case suggesting a novel undescribed mechanism of formation
J Milosevic, L El Khattabi, A Roubergue, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences
|
November 4, 2019
Role of P-glycoprotein in the brain disposition of seletalisib: Evaluation of the potential for drug-drug interactions
Jean-Marie Nicolas, Hugues Chanteux, Johan Nicolaï, et al.
Applied Radiation and Isotopes : Including Data, Instrumentation and Methods for Use in Agriculture, Industry and Medicine
|
March 28, 2015
Development of a freeze-dried kit formulation for the preparation of 99mTc-NTP 15-5, a radiotracer for scintigraphic imaging of proteoglycans
Aurélien Vidal, Vincent Gaumet, Marie-Josèphe Galmier, et al.
Prenatal Diagnosis
|
March 12, 1999
Prenatal detection of a 1p36 deletion in a fetus with multiple malformations and a review of the literature
L Faivre, N Morichon-Delvallez, G Viot, et al.
Journal of Medical Genetics
|
October 4, 2002
Homozygosity mapping of a Dyggve-Melchior-Clausen syndrome gene to chromosome 18q21.1
C Thauvin-Robinet, V El Ghouzzi, W Chemaitilly, et al.
Gynecologie, Obstetrique, Fertilite & Senologie
|
February 15, 2020
[Adverse obstetric and perinatal outcome with in vitro fertilization technology: A French nationwide population-based study]
F Pessione, J De Mouzon, A Deveaux, et al.
Reproductive Biomedicine Online
|
March 3, 2023
Risk factors associated with preterm birth in singletons born after IVF: a national cohort study
Marie-Josée Gervoise-Boyer, Patricia Fauque, Jacques De Mouzon, et al.
European Journal of Radiology
|
December 17, 2013
CMR assessment after a transapical-transcatheter aortic valve implantation
Loïc Biere, Frédéric Pinaud, Stéphane Delépine, et al.
Page
of 23