Janice M. Fletcher
72 King William Road
North Adelaide, SA 5006, Australia
North Adelaide, SA 5006, Australia
Last Updated: 09/26/2026
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Found 44 publications
Nationwide, Couple-Based Genetic Carrier Screening.
Journal: The New England journal of medicine
Published: November 20, 2024
The Australian Genomics Mitochondrial Flagship: A national program delivering mitochondrial diagnoses.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: April 04, 2024
Extending the new era of genomic testing into pregnancy management: A proposed model for Australian prenatal services.
Journal: The Australian & New Zealand journal of obstetrics & gynaecology
Published: November 12, 2023
Poor patient outcome correlates with active engulfment of cytokeratin positive CTCs within cancer-associated monocyte population in lung cancer.
Journal: Clinical & experimental metastasis
Published: October 15, 2023
Consumers lived experiences and satisfaction with sub-acute mental health residential services.
Journal: Social psychiatry and psychiatric epidemiology
Published: September 11, 2023
Narrowing the diagnostic gap: Genomes, episignatures, long-read sequencing, and health economic analyses in an exome-negative intellectual disability cohort.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: June 30, 2023
The relationship between beta-ureidopropionase deficiency due to UPB1 variants and human phenotypes is uncertain.
Journal: Molecular genetics and metabolism
Published: April 06, 2022
Corrigendum to "Comparative analysis of brain pathology in heparan sulphate storing mucopolysaccharidosis" [Molecular Genetics and Metabolism 131 (2020) pages 197-205].
Journal: Molecular genetics and metabolism
Published: December 27, 2021
Deleterious variants in CRLS1 lead to cardiolipin deficiency and cause an autosomal recessive multi-system mitochondrial disease.
Journal: Human molecular genetics
Published: October 25, 2021
Challenges in Diagnosing Intermediate Maple Syrup Urine Disease by Newborn Screening and Functional Validation of Genomic Results Imperative for Reproductive Family Planning.
Journal: International journal of neonatal screening
Published: March 27, 2021
Fatal perinatal mitochondrial cardiac failure caused by recurrent de novo duplications in the ATAD3 locus.
Journal: Med (New York, N.Y.)
Published: February 12, 2021
Isolated autism is not an indication for Smith-Lemli-Opitz syndrome biochemical testing.
Journal: Journal of paediatrics and child health
Published: December 23, 2020
Last Updated: 09/26/2026