Tristan S E Hardy

5PUBLICATIONS
12CO-AUTHORS
Foetal development and medicineDevelopmental genetics (incl. sex determination)Haematological tumoursMedical biotechnology diagnostics (incl. biosensors)Neurogenetics
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Publications (5)

|Sep 08, 2021
Preimplantation Genetic Testing for Monogenic Conditions: Is Cell-Free DNA Testing the Next Step?

Alice Rogers, Melody Menezes, Stefan C Kane

|Nov 16, 2020
Aberrant Splicing of SDHC in Families With Unexplained Succinate Dehydrogenase-Deficient Paragangliomas.

Sunita M C De Sousa, John Toubia, Tristan S E Hardy

|Mar 07, 2020
Paternal mosaicism for a novel PBX1 mutation associated with recurrent perinatal death: Phenotypic expansion of the PBX1-related syndrome.

Peer Arts, Jessica Garland, Alicia B Byrne

|Feb 11, 2020
The role of prenatal diagnosis following preimplantation genetic testing for single-gene conditions: A historical overview of evolving technologies and clinical practice.

Tristan Hardy

|Aug 07, 2019
The next generation of noninvasive fetal genotyping and the return to single gene conditions.

T Hardy

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Frequent Collaborators

2 joint publications

Hamish S Scott

1 joint publications

Alice Rogers

1 joint publications

Melody Menezes

1 joint publications

Stefan C Kane