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The Application of Clinical Genetics|July 16, 2016
Alagille syndrome: clinical perspectivesMaha Saleh, Binita M Kamath, David Chitayat
Clinical Case Reports|September 13, 2021
Resolving severe oligohydramnios as an early prenatal presentation of renal coloboma syndrome-A report of two generationsAndrew Nguyen, Carla Campagnolo, Ghislain Hardy, et al.
The Clinical Teacher|February 8, 2022
Genetic simulation for high-stakes conversationsMaha Saleh, Andrea Shugar, Alison Dodds, et al.
Ophthalmic Genetics|December 27, 2021
OTX2 mutation associated with severe myopia in a Canadian familySnow Wangding, Samantha Colaiacovo, Inas Makar, et al.
Clinical Genetics|November 2, 2022
A novel MAP3K7 mutation in a child with cardiospondylocarpofacial syndrome and orofacial cleftingWilliam Billal Shepherd, Samantha Colaiacovo, Craig Campbell, et al.
Molecular Genetics & Genomic Medicine|September 4, 2020
TP63-mutation as a cause of prenatal lethal multicystic dysplastic kidneysIsabel Friedmann, Carla Campagnolo, Nancy Chan, et al.
Clinical Case Reports|August 2, 2023
An uninformative NIPT as an early indicator of cri-du-chat due to a chromosomal 5;18 translocation-An atypical presentation of a rare cytogenetic phenomenonDevanshi Shukla, Matthew Dinunzio, Samantha Colaiacovo, et al.
Frontiers in Behavioral Neuroscience|August 9, 2021
A Review of Working Memory Training in the Management of Attention Deficit Hyperactivity DisorderMaha Saleh Habsan Al-Saad, Basma Al-Jabri, Abeer F Almarzouki
Prenatal Diagnosis|December 15, 2017
Nonisolated diaphragmatic hernia in Simpson-Golabi-Behmel syndromeKaren Chong, Maha Saleh, Marie Injeyan, et al.
Pediatric Neurology|October 2, 2013
Brain arteriovenous malformations in patients with hereditary hemorrhagic telangiectasia: clinical presentation and anatomical distributionMaha Saleh, Melissa T Carter, Giuseppe A Latino, et al.
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