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IEEE Transactions on Bio-Medical Engineering|July 12, 2018
Robotic Immobilization of Motile Sperm for Clinical Intracytoplasmic Sperm InjectionZhuoran Zhang, Changsheng Dai, James Huang, 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|July 22, 2005
Cavum veli interpositi: prenatal diagnosis and postnatal outcomePrakesh S Shah, Susan Blaser, Ants Toi, 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.
American Journal of Human Genetics|May 23, 2002
Connection between elastin haploinsufficiency and increased cell proliferation in patients with supravalvular aortic stenosis and Williams-Beuren syndromeZsolt Urbán, Sheila Riazi, Thomas L Seidl, 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.
American Journal of Medical Genetics. Part A|November 15, 2007
Raine syndrome: a rare lethal osteosclerotic bone dysplasia. Prenatal diagnosis, autopsy, and neuropathological findingsDavid Chitayat, Patrick Shannon, Sarah Keating, 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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