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Molecular Human Reproduction|November 9, 2006
Epithelial-mesenchymal transition process in human embryonic stem cells cultured in feeder-free conditionsU Ullmann, P In't Veld, C Gilles, et al.The New England Journal of Medicine|June 1, 1995
Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferensM Chillón, T Casals, B Mercier, et al.European Journal of Pediatrics|September 15, 1999
Cerebral palsy and pyruvate dehydrogenase deficiency: identification of two new mutations in the E1alpha geneW Lissens, P Vreken, P G Barth, et al.Human Reproduction (Oxford, England)|November 20, 2004
ESHRE PGD Consortium data collection IV: May-December 2001K Sermon, C Moutou, J Harper, et al.Prenatal Diagnosis|January 26, 2002
Strategies for prenatal and preimplantation genetic diagnosis in Marfan syndrome (MFS)B Loeys, L Nuytinck, P Van Acker, et al.Human Reproduction (Oxford, England)|January 6, 2007
Single embryo transfer in preimplantation genetic diagnosis cycles for women <36 years does not reduce delivery rateP Donoso, W Verpoest, E G Papanikolaou, et al.Scientific Reports|April 16, 2021
Sustained intrinsic WNT and BMP4 activation impairs hESC differentiation to definitive endoderm and drives the cells towards extra-embryonic mesodermC Markouli, E Couvreu De Deckersberg, D Dziedzicka, et al.Pediatric Research|March 1, 1993
E1 pyruvate dehydrogenase deficiency in a child with motor neuropathyG Bonne, C Benelli, L De Meirleir, et al.Journal of Clinical Pathology|February 3, 2009
Immunohistochemical analysis of the oxidative phosphorylation complexes in skeletal muscle from patients with mitochondrial DNA encoded tRNA gene defectsB De Paepe, J Smet, M Lammens, et al.Journal of Inherited Metabolic Disease|March 21, 1998
Pyruvate dehydrogenase complex deficiency and absence of subunit XL De Meirleir, W Lissens, C Benelli, et al.Pageof 19