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European Journal of Human Genetics : EJHG|June 26, 2014
Prenatal growth restriction, retinal dystrophy, diabetes insipidus and white matter disease: expanding the spectrum of PRPS1-related disordersAlmundher Al-Maawali, Lucie Dupuis, Susan Blaser, et al.Journal of Medical Genetics|September 21, 2021
Clinical application of fetal genome-wide sequencing during pregnancy: position statement of the Canadian College of Medical GeneticistsJoanna Lazier, Taila Hartley, Jo-Ann Brock, et al.American Journal of Medical Genetics. Part A|May 29, 2012
Definition of a critical genetic interval related to kidney abnormalities in the Potocki-Lupski syndromeElaine Suk-Ying Goh, Irene C Perez, Cesar P Canales, et al.The Journal of Clinical Psychiatry|October 5, 2021
Correction. Reproductive Safety of Second-Generation Antipsychotics: Updated Data From the Massachusetts General Hospital National Pregnancy Registry for Atypical AntipsychoticsAdele C Viguera, Marlene P Freeman, Lina Góez-Mogollón, et al.Journal of Obstetrics and Gynaecology Canada : JOGC = Journal D'Obstetrique Et Gynecologie Du Canada : JOGC|November 6, 2010
Prenatal exposure to mycophenolate mofetil: an updated estimateChagit Klieger-Grossmann, David Chitayat, Sharon Lavign, et al.The Journal of Clinical Psychiatry|August 5, 2021
Reproductive Safety of Second-Generation Antipsychotics: Updated Data From the Massachusetts General Hospital National Pregnancy Registry for Atypical AntipsychoticsAdele C Viguera, Marlene P Freeman, Lina Góez-Mogollón, et al.Fetal Diagnosis and Therapy|January 19, 2026
The Evolution of Cephalocentesis in Contemporary Obstetric Practice: From Emergency Intervention to Planned ProcedureCatherine Windrim, Yada Kunpalin, Alyaa AlRefai, et al.American Journal of Medical Genetics. Part A|October 26, 2023
45,X/46,XY mosaicism: Clinical manifestations and long term follow-upEbba Alkhunaizi, Jenna Plamondon Albrecht, Mahmoud Aarabi, et al.American Journal of Medical Genetics. Part A|November 27, 2018
Gain-of-function variants in the ODC1 gene cause a syndromic neurodevelopmental disorder associated with macrocephaly, alopecia, dysmorphic features, and neuroimaging abnormalitiesLance H Rodan, Kwame Anyane-Yeboa, Karen Chong, et al.American Journal of Human Genetics|October 22, 2019
Bi-allelic Pathogenic Variants in TUBGCP2 Cause Microcephaly and Lissencephaly Spectrum DisordersTadahiro Mitani, Jaya Punetha, Ibrahim Akalin, et al.Pageof 53