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Journal of Obstetrics and Gynaecology Canada : JOGC = Journal D'Obstetrique Et Gynecologie Du Canada : JOGC|June 13, 2013
Multidisciplinary management of invasive placenta previaMelissa G Walker, Lisa Allen, Rory C Windrim, et al.
Prenatal Diagnosis|July 10, 2013
Dyssegmental dysplasia, Silverman-Handmaker type: prenatal ultrasound findings and molecular analysisNoor Niyar N Ladhani, David Chitayat, Marjan M Nezarati, et al.
American Journal of Medical Genetics. Part A|November 14, 2008
Chondrodysplasia punctata associated with maternal autoimmune diseases: expanding the spectrum from systemic lupus erythematosus (SLE) to mixed connective tissue disease (MCTD) and scleroderma report of eight casesDavid Chitayat, Sarah Keating, Dina J Zand, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|February 1, 2019
Placental mesenchymal dysplasia: An underdiagnosed placental pathology with various clinical outcomesCécile Guenot, John Kingdom, Maud De Rham, et al.
Frontiers in Endocrinology|April 6, 2019
Failure of Decidualization and Maternal Immune Tolerance Underlies Uterovascular Resistance in Intra Uterine Growth RestrictionCaroline Dunk, Melissa Kwan, Aleah Hazan, et al.
American Journal of Medical Genetics. Part A|May 17, 2007
The PDAC syndrome (pulmonary hypoplasia/agenesis, diaphragmatic hernia/eventration, anophthalmia/microphthalmia, and cardiac defect) (Spear syndrome, Matthew-Wood syndrome): report of eight cases including a living child and further evidence for autosomal recessive inheritanceDavid Chitayat, Hana Sroka, Sarah Keating, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|August 15, 2015
The Placental Distal Villous Hypoplasia Pattern: Interobserver Agreement and Automated Fractal Dimension as an Objective MetricAnika Mukherjee, Adrian D C Chan, Sarah Keating, et al.
American Journal of Obstetrics and Gynecology|October 18, 2015
The hemodynamics of late-onset intrauterine growth restriction by MRIMeng Yuan Zhu, Natasha Milligan, Sarah Keating, et al.
Nucleic Acids Research|November 22, 2014
BioModels: ten-year anniversaryVijayalakshmi Chelliah, Nick Juty, Ishan Ajmera, et al.
American Journal of Human Genetics|February 3, 2007
Mutations in STRA6 cause a broad spectrum of malformations including anophthalmia, congenital heart defects, diaphragmatic hernia, alveolar capillary dysplasia, lung hypoplasia, and mental retardationFrancesca Pasutto, Heinrich Sticht, Gerhard Hammersen, et al.
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