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Prospective cohort study of genomic newborn screening: BabyScreen+ pilot study protocol.

• Authors : Lunke S; Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Parkville, Victoria, Australia.; University of Melbourne, Melbourne, Victoria, Australia.

Subjects: Neonatal Screening* ; Genomics*; Child

• Source: BMJ open [BMJ Open] 2024 Apr 03; Vol. 14 (4), pp. e081426. Date of Electronic Publication: 2024 Apr 03.Publisher: BMJ Publishing Group Ltd Country of Publication: England NLM ID: 101552874 Publication Model: Electronic Cited Medium: Internet ISSN:

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Personal utility of genomic sequencing for infants with congenital deafness.

• Authors : Tutty E; Department of Paediatrics, The University of Melbourne, Melbourne, Victoria, Australia.; Murdoch Children's Research Institute, Melbourne, Victoria, Australia.

Subjects: Genetic Testing* ; Genomics*; Deafness/Deafness/Deafness/*diagnosis

• Source: American journal of medical genetics. Part A [Am J Med Genet A] 2021 Dec; Vol. 185 (12), pp. 3634-3643. Date of Electronic Publication: 2021 Jun 29.Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Agricola

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The expectations and realities of nutrigenomic testing in australia: A qualitative study.

• Authors : Tutty, Erin; Hickerton, Chriselle; Terrill, Bronwyn

Subjects: NUTRITIONAL assessment; ATTITUDE (Psychology); RESEARCH methodologyAUSTRALIA

• Source: Health Expectations. Apr2021, Vol. 24 Issue 2, p670-686. 17p. 3 Diagrams, 4 Charts.

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