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Prenatal Diagnosis|October 10, 2013
No evidence for mutations in NLRP7 and KHDC3L in women with androgenetic hydatidiform molesSangeetha Mahadevan, Shu Wen, Alfred Balasa, et al.
Molecular Genetics and Metabolism|March 19, 2011
Atypical presentation of Leigh syndrome associated with a Leber hereditary optic neuropathy primary mitochondrial DNA mutationGary Fruhman, Megan L Landsverk, Timothy E Lotze, et al.
American Journal of Perinatology|December 10, 2021
The Risk of Readmission after Early Postpartum Discharge during the COVID-19 PandemicMoti Gulersen, Gregg Husk, Erez Lenchner, et al.
European Journal of Human Genetics : EJHG|January 21, 2011
The phenotype of recurrent 10q22q23 deletions and duplicationsBregje W M van Bon, Jorune Balciuniene, Gary Fruhman, et al.
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