Canlyniadau Chwilio - Wedderburn, Sarah

The new genomic medicine service and implications for patients  gan Snape, Katie, Wedderburn, Sarah, Barwell, Julian

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Should All Individuals Be Screened for Genetic Predisposition to Cancer? gan Wedderburn, Sarah, McVeigh, Terri P.

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Hereditary Neuropathy with Liability to Pressure Palsy Presenting as an Acute Brachial Plexopathy: A Lover's Palsy gan Wedderburn, Sarah, Pateria, Puraskar, Panegyres, Peter K.

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Update: variable implementation of the 2018 UKCGG/UKGTN guidelines for breast cancer gene panel tests offered by UK genetics services gan Wedderburn, Sarah, Archer, Stephanie, Tischkowitz, Marc, Hanson, Helen

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Towards establishing consistency in triage in a tertiary specialty gan McVeigh, Terri Patricia, Donnelly, Deirdre, Al Shehhi, Maryam, Jones, Elizabeth A., Murray, Alexandra, Wedderburn, Sarah, Porteous, Mary, Lynch, Sally Ann

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Identification of LAMA1 mutations ends diagnostic odyssey and has prognostic implications for patients with presumed Joubert syndrome gan Powell, Laura, Olinger, Eric, Wedderburn, Sarah, Ramakumaran, Vijayalakshmi Salem, Kini, Usha, Clayton-Smith, Jill, Ramsden, Simon C, Rice, Sarah J, Barroso-Gil, Miguel, Wilson, Ian, Cowley, Lorraine, Johnson, Sally, Harris, Elizabeth, Montgomery, Tara, Bertoli, Marta, Boltshauser, Eugen, Sayer, John A

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