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Clinical Genetics|February 25, 2021
Heterozygous NOTCH1 deletion associated with variable congenital heart defectsMaian Roifman, Brian Hon Yin Chung, Diane Myles Reid, et al.
Systems Biology in Reproductive Medicine|September 24, 2014
PGD for a carrier of an intrachromosomal insertion using aCGHClaire Ann Jones, Elena Kolomietz, Georges Maire, et al.
Epigenetics|April 9, 2011
WNT2 promoter methylation in human placenta is associated with low birthweight percentile in the neonateJose C Ferreira, Sanaa Choufani, Daria Grafodatskaya, et al.
American Journal of Medical Genetics. Part A|August 25, 2004
Abnormal pericyte recruitment as a cause for pulmonary hypertension in Adams-Oliver syndromeMillan S Patel, Glenn P Taylor, Simi Bharya, et al.
American Journal of Obstetrics and Gynecology|March 9, 2006
Second-trimester prediction of severe placental complications in women with combined elevations in alpha-fetoprotein and human chorionic gonadotrophinFawaz Alkazaleh, Vandana Chaddha, Sandra Viero, et al.
The American Journal of Pathology|July 23, 2013
Fetal reprogramming and senescence in hypoplastic left heart syndrome and in human pluripotent stem cells during cardiac differentiationNaila Gaber, Mark Gagliardi, Pranali Patel, et al.
Circulation|July 31, 2002
Fetal cardiomyopathies: pathogenic mechanisms, hemodynamic findings, and clinical outcomeSimone R F F Pedra, Jeffrey F Smallhorn, Greg Ryan, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|January 21, 2021
Brain and Placental Pathology in Fetal COL4A1 Related DiseasePatrick Shannon, Courtney Hum, Tony Parks, et al.
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