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A H Trainer

Showing results (11-20 of 14) with videos related to

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Familial Cancer|May 10, 2020
Evaluation of implementation of risk management guidelines for carriers of pathogenic variants in mismatch repair genes: a nationwide audit of familial cancer clinicsB Meiser, R Kaur, J Kirk, et al.
Journal of Medical Genetics|March 10, 2001
Clinical studies on submicroscopic subtelomeric rearrangements: a checklistB B de Vries, S M White, S J Knight, et al.
Journal of Medical Genetics|July 4, 2009
Phenotypic variability in 49 cases of ESCO2 mutations, including novel missense and codon deletion in the acetyltransferase domain, correlates with ESCO2 expression and establishes the clinical criteria for Roberts syndromeH Vega, A H Trainer, M Gordillo, et al.
British Journal of Cancer|June 22, 2013
Tumour morphology predicts PALB2 germline mutation statusZ L Teo, E Provenzano, G S Dite, et al.
Pageof 2

Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
Familial Cancer|May 10, 2020
Evaluation of implementation of risk management guidelines for carriers of pathogenic variants in mismatch repair genes: a nationwide audit of familial cancer clinicsB Meiser, R Kaur, J Kirk, et al.
Journal of Medical Genetics|March 10, 2001
Clinical studies on submicroscopic subtelomeric rearrangements: a checklistB B de Vries, S M White, S J Knight, et al.
Journal of Medical Genetics|July 4, 2009
Phenotypic variability in 49 cases of ESCO2 mutations, including novel missense and codon deletion in the acetyltransferase domain, correlates with ESCO2 expression and establishes the clinical criteria for Roberts syndromeH Vega, A H Trainer, M Gordillo, et al.
British Journal of Cancer|June 22, 2013
Tumour morphology predicts PALB2 germline mutation statusZ L Teo, E Provenzano, G S Dite, et al.
Pageof 2