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Epilepsia|April 20, 2007
Evaluation of subcortical white matter and deep white matter tracts in malformations of cortical developmentElysa Widjaja, Susan Blaser, Elka Miller, et al.
Prenatal Diagnosis|February 27, 2009
Cornelia de Lange syndrome (CdLS): prenatal and autopsy findingsKaren Chong, Sarah Keating, Stephanie Hurst, et al.
Prenatal Diagnosis|November 7, 2006
X-Linked dominant chondrodysplasia punctata: prenatal diagnosis and autopsy findingsShalini Umranikar, Phyllis Glanc, Sheila Unger, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|September 28, 2006
A novel GDAP1 mutation 439delA is associated with autosomal recessive CMT diseaseDomna-Maria Georgiou, Paschalis Nicolaou, David Chitayat, et al.
Prenatal Diagnosis|December 10, 2016
Mutations in the NEB gene cause fetal akinesia/arthrogryposis multiplex congenitaMichal Feingold-Zadok, David Chitayat, Karen Chong, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|June 24, 2020
Fetal Meconium Peritonitis - Prenatal Findings and Postnatal Outcome: A Case Series, Systematic Review, and Meta-AnalysisShiri Shinar, Swati Agrawal, Michelle Ryu, et al.
Pediatric Research|June 19, 2015
The ontogeny of P-glycoprotein in the developing human blood-brain barrier: implication for opioid toxicity in neonatesJessica Lam, Stephanie Baello, Majid Iqbal, et al.
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