Carolyn Shalhoub
Sydney, NSW, Australia
Last Updated: 09/26/2026
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Found 9 publications
I've Never Heard of This! An Approach to Child and Family-Centred Care for Children and Young People With Rare Diseases.
Journal: Journal of paediatrics and child health
Published: May 02, 2025
International Clinical Evidence-based Guideline for Kleefstra Syndrome.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: February 14, 2025
International clinical evidence-based guideline for Kleefstra syndrome.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: February 14, 2025
Implementation and Evaluation of a National Multidisciplinary Kidney Genetics Clinic Network Over 10 Years.
Journal: Kidney international reports
Published: March 01, 2024
Integration of EpiSign, facial phenotyping, and likelihood ratio interpretation of clinical abnormalities in the re-classification of an ARID1B missense variant.
Journal: American journal of medical genetics. Part C, Seminars in medical genetics
Published: July 13, 2023
OTX2 duplications: a recurrent cause of oculo-auriculo-vertebral spectrum.
Journal: Journal of medical genetics
Published: July 04, 2022
Professional regulation for Australasian genetic counselors.
Journal: Journal of genetic counseling
Published: April 29, 2020
Differences in Outcomes between Early and Late Diagnosis of Cystic Fibrosis in the Newborn Screening Era.
Journal: The Journal of pediatrics
Published: June 04, 2016
Showing 1-9 of 9
Last Updated: 09/26/2026