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The Anatomical Record. Part A, Discoveries in Molecular, Cellular, and Evolutionary Biology|May 25, 2005
Reelin immunoreactivity in lymphatics and liver during development and adult lifeBrigitte Samama, Nelly Boehm
Gynecologic Oncology|April 5, 2008
P16 expression in relation to human papillomavirus in liquid-based cervical smearsBrigitte Samama, Christiane Schaeffer, Nelly Boehm
Human Pathology|May 2, 2006
p16 expression in relation to human papillomavirus in anogenital lesionsBrigitte Samama, Dan Lipsker, Nelly Boehm
European Journal of Dermatology : EJD|February 18, 2004
Retinoic-acid receptor beta expression in melanocytesNelly Boehm, Brigitte Samama, Bernard Cribier, et al.
Plos One|August 14, 2015
Human Neural Cells Transiently Express Reelin during Olfactory Placode DevelopmentM Cristina Antal, Brigitte Samama, M Said Ghandour, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|October 5, 2002
HPV DNA detection by in situ hybridization with catalyzed signal amplification on thin-layer cervical smearsBrigitte Samama, Salomé Plas-Roser, Christiane Schaeffer, et al.
Plos One|January 26, 2017
Adenylate Cyclase Type III Is Not a Ubiquitous Marker for All Primary Cilia during DevelopmentMaria Cristina Antal, Karelle Bénardais, Brigitte Samama, et al.
Frontiers in Cellular Neuroscience|December 12, 2022
Oligodendroglial primary cilium heterogeneity during development and demyelination/remyelinationGiada Delfino, Karelle Bénardais, Julien Graff, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|September 1, 2009
Contribution of 3D ultrasound and fetal face studies to the prenatal diagnosis of Pallister-Killian syndromeNicolas Sananes, Virginie Guigue, Christophe Vayssiere, et al.
European Journal of Human Genetics : EJHG|May 26, 2005
Trisomy 7 mosaicism, maternal uniparental heterodisomy 7 and Hirschsprung's disease in a child with Silver-Russell syndromeElisabeth Flori, Emmanuelle Girodon, Brigitte Samama, et al.
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