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Prenatal Diagnosis|April 3, 2012
Multiplex ligation-dependent probe amplification (MLPA) and prenatal diagnosisAlecia S Willis, Ignatia van den Veyver, Christine M EngJournal of Genetic Counseling|July 8, 2022
Lack of consensus among healthcare professionals at a large academic medical center on the use of exome sequencing for prenatal diagnosisKylie Johnson, Hadi Erfani, Mohamad Ali Maktabi, et al.American Journal of Medical Genetics. Part A|October 18, 2008
Neuroimaging aspects of Aicardi syndromeBobbi Hopkins, V Reid Sutton, Richard Alan Lewis, et al.American Journal of Perinatology|September 29, 2009
Pheochromocytoma and Von Hippel-Lindau in pregnancyNonna Kolomeyevskaya, Maria Blazo, Ignatia Van den Veyver, et al.American Journal of Perinatology|May 12, 2010
Management of ornithine transcarbamylase deficiency in pregnancyHector Mendez-Figueroa, Kerri Lamance, V Reid Sutton, et al.Prenatal Diagnosis|July 3, 2016
Comparison of three whole genome amplification methods for detection of genomic aberrations in single cellsElizabeth Normand, Sadeem Qdaisat, Weimin Bi, et al.Prenatal Diagnosis|June 29, 2022
Circulating trophoblast numbers as a potential marker for pregnancy complicationsBrielle Crovetti, Mohamad Ali Maktabi, Hadi Erfani, et al.Plos One|April 15, 2021
Use of amplicon-based sequencing for testing fetal identity and monogenic traits with Single Circulating Trophoblast (SCT) as one form of cell-based NIPTXinming Zhuo, Qun Wang, Liesbeth Vossaert, et al.Cell Reports|December 4, 2014
A rare human syndrome provides genetic evidence that WNT signaling is required for reprogramming of fibroblasts to induced pluripotent stem cellsJason Ross, Julia Busch, Ellen Mintz, et al.Prenatal Diagnosis|July 7, 2011
Genome-wide array-based copy number profiling in human placentas from unexplained stillbirthsR Alan Harris, Francesca Ferrari, Shay Ben-Shachar, et al.Pageof 2