E-LIB Suche - Ergebnisse für: Mary McPhillips

1

Correction: When is a mutation not a mutation: the case of ..:

Wong-Brown, Michelle ; McPhillips, Mary ; Gleeson, Margaret...
Hereditary Cancer in Clinical Practice. 20 (2022) 1 - p. , 2022

Link: https://doi.org/10.1186/..

2

CTNNB1 exon 3 mutations in desmoid and other tumours:

Billings, Raewyn ; Ashton, Katie A. ; Tucker, Kathy...
Pathology. 53 (2021) - p. S41 , 2021

Link: https://doi.org/10.1016/..

3

Novel de novo TRIP12 mutation reveals variable phenotypic p..:

Donoghue, Tess ; Garrity, Lauren ; Ziolkowski, Andrew...
American Journal of Medical Genetics Part A. 182 (2020) 7 - p. 1801-1806 , 2020

Link: https://doi.org/10.1002/..

4

Targeted sequencing of genes associated with the mismatch r..:

Singh, Ashish Kumar ; Talseth-Palmer, Bente ; McPhillips, Mary...
PLOS ONE. 15 (2020) 7 - p. e0235613 , 2020

Link: https://doi.org/10.1371/..

5

Lynch syndrome mutation spectrum in New South Wales, Austra..:

Sjursen, Wenche ; McPhillips, Mary ; Scott, Rodney J..
Molecular Genetics & Genomic Medicine. 4 (2016) 2 - p. 223-231 , 2016

Link: https://doi.org/10.1002/..

6

Targeted next‐generation sequencing of 22 mismatch repair g..:

Talseth‐Palmer, Bente A. ; Bauer, Denis C. ; Sjursen, Wenche...
Cancer Medicine. 5 (2016) 5 - p. 929-941 , 2016

Link: https://doi.org/10.1002/..

7

When is a mutation not a mutation: the case of the c.594-2A..:

Wong-Brown, Michelle ; McPhillips, Mary ; Gleeson, Margaret...
Hereditary Cancer in Clinical Practice. 14 (2016) 1 - p. , 2016

Link: https://doi.org/10.1186/..

8

The curious case of a woman with two BRCA1 mutations in tra..:

Scott, Rodney J ; Wong-Brown, Michelle ; McPhillips, Mary...
Hereditary Cancer in Clinical Practice. 13 (2015) S2 - p. , 2015

Link: https://doi.org/10.1186/..

9

Chromosome 8q23.3, 10p14 and 11q23.1 variants modify colore..:

Talseth-Palmer, Bente A ; Wijnen, Juul T ; Brenne, Ingvild S...
Hereditary Cancer in Clinical Practice. 10 (2012) Suppl 2 - p. A32 , 2012

Link: https://doi.org/10.1186/..

10

Combined analysis of three lynch syndrome cohorts confirms ..:

Talseth‐Palmer, Bente A. ; Wijnen, Juul T. ; Brenne, Ingvild S....
International Journal of Cancer. 132 (2012) 7 - p. 1556-1564 , 2012

Link: https://doi.org/10.1002/..

11

MSH6 and PMS2 mutation positive Australian Lynch syndrome f..:

Talseth-Palmer, Bente A ; McPhillips, Mary ; Groombridge, Claire..
Hereditary Cancer in Clinical Practice. 8 (2010) 1 - p. , 2010

Link: https://doi.org/10.1186/..

12

The Association of the COMT V158M Polymorphism with Endomet..:

Ashton, Katie A ; Meldrum, Cliff J ; McPhillips, Mary L...
Hereditary Cancer in Clinical Practice. 4 (2006) 2 - p. 94 , 2006

Link: https://doi.org/10.1186/..

13

Frequency of the Common MYH Mutations (G382D and Y165C) in ..:

Ashton, Katie A. ; Meldrum, Cliff J. ; McPhillips, Mary L...
Hereditary Cancer in Clinical Practice. 3 (2005) 2 - p. , 2005

Link: https://doi.org/10.1186/..

14

Deletion Mutations in an Australian Series of HNPCC Patient:

McPhillips, Mary ; Meldrum, Cliff J ; Creegan, Rhona..
Hereditary Cancer in Clinical Practice. 3 (2005) 1 - p. , 2005

Link: https://doi.org/10.1186/..

15

A Comparison Between Denaturing Gradient Gel Electrophoresi..:

Meldrum, Cliff J. ; McPhillips, Mary ; Crooks, Renee...
Hereditary Cancer in Clinical Practice. 1 (2003) 1 - p. , 2003

Link: https://doi.org/10.1186/..