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Human Reproduction (Oxford, England)|February 22, 2013
Chorionic villous vascularization related to phenotype and genotype in first trimester miscarriages in a recurrent pregnancy loss cohortAveril D Reus, Mary D Stephenson, Frederique M van Dunné, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|January 22, 2013
Histological findings in unclassified sudden infant death, including sudden infant death syndromeGermaine Liebrechts-Akkerman, Judith V M G Bovée, Liliane C D Wijnaendts, et al.
Endocrine Pathology|January 12, 2021
What Have We Learned from Molecular Biology of Paragangliomas and Pheochromocytomas?Thomas G Papathomas, Diederik P D Suurd, Karel Pacak, et al.
Molecular Syndromology|August 18, 2015
Phenotypic Variability Associated with a Large Recurrent 1q21.1 Microduplication in a Three-Generation FamilyJudith M A Verhagen, Nicole de Leeuw, Dimitri N M Papatsonis, et al.
The Journal of Pathology|February 10, 2021
TRIM28 variants and Wilms' tumour predispositionJanna A Hol, Illja J Diets, Ronald R de Krijger, et al.
Neonatology|June 17, 2010
Effect of oxygen on the expression of hypoxia-inducible factors in human fetal lung explantsPrapapan Rajatapiti, Jessica D de Rooij, Leonardus W J E Beurskens, et al.
The American Journal of Pathology|December 29, 2011
High anaplastic lymphoma kinase immunohistochemical staining in neuroblastoma and ganglioneuroblastoma is an independent predictor of poor outcomeFloor A M Duijkers, José Gaal, Jules P P Meijerink, et al.
Virchows Archiv : an International Journal of Pathology|August 19, 2019
Correction to: Eosinophilic myenteric ganglionitis as a cause of chronic intestinal pseudo-obstructionAriadne H A G Ooms, Joanne Verheij, Jessie M Hulst, et al.
Mediastinum (Hong Kong, China)|June 1, 2023
Asymptomatic lipofibroadenoma in a 17-year-old male: a case report and literature review of a rare entityMichael A den Bakker, Marijn A Vermeulen, Cornelis P van de Ven, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|October 6, 1999
CHARGE association-related ocular pathology in a newborn with partial trisomy 19q and partial monosomy 21q, from a maternal translocation (19;21) (q13.1;q22.3)R R De Krijger, C M Mooy, J O Van Hemel, et al.
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