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Molecular Syndromology|April 8, 2020
Robinow Syndrome and Brachydactyly: An Interplay of High-Throughput Sequencing and Deep Phenotyping in a KindredRanjana Mishra, Vibha Jain, Deepti Gupta, et al.Women and Birth : Journal of the Australian College of Midwives|December 5, 2019
Measuring respect and autonomy in Dutch maternity care: Applicability of two measuresE I Feijen-de Jong, M van der Pijl, S Vedam, et al.Molecular Vision|November 17, 2005
Genetic homogeneity for inherited congenital microcoria loci in an Asian Indian pedigreeVedam Lakshmi Ramprasad, Sarangapani Sripriya, George Ronnie, et al.Analytical Chemistry|February 1, 2018
Mass Spectrometric Methodologies for Investigating the Metabolic Signatures of Parkinson's Disease: Current Progress and Future PerspectivesEmily L Gill, Jeremy P Koelmel, Richard A Yost, et al.Maternal and Child Health Journal|November 24, 2021
The Impact of Culturally-Centered Care on Peripartum Experiences of Autonomy and Respect in Community Birth Centers: A Comparative StudyJennifer I Almanza, J 'Mag Karbeah, Katelyn M Tessier, et al.Journal of Bacteriology|March 4, 2006
The pea nodule environment restores the ability of a Rhizobium leguminosarum lipopolysaccharide acpXL mutant to add 27-hydroxyoctacosanoic acid to its lipid AVinata Vedam, Elmar Kannenberg, Anup Datta, et al.Health Policy and Planning|April 16, 2022
Advancing quality and safety of perinatal services in India: opportunities for effective midwifery integrationSaraswathi Vedam, Reena Titoria, Paulomi Niles, et al.Clinical Genetics|December 10, 2023
Diagnostic exome identifies a novel PRKG2 mutation in a proband with skeletal dysplasiaPayal Kamdar, Thenral S Geetha, Thomas Palocaren, et al.Postgraduate Medical Journal|August 14, 2020
Prevalence and factors associated with advanced care directives in a motor neuron disease multidisciplinary clinic in AustraliaChun Seng Phua, Aloysius Ng, Christopher Brooks, et al.Pharmacogenomics|August 2, 2019
Resequencing CYP2D6 gene in Indian population: CYP2D6*41 identified as the major reduced function alleleAarthi Manoharan, Deepak Gopal Shewade, Pradeep Anand Ravindranath, et al.Pageof 30