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Plos One
|
December 30, 2011
An 11p15 imprinting centre region 2 deletion in a family with Beckwith Wiedemann syndrome provides insights into imprinting control at CDKN1C
Elizabeth Algar, Vinod Dagar, Menka Sebaj, et al.
Histopathology
|
May 1, 2018
Peritumoral granulomatous reaction in endometrial carcinoma: association with DNA mismatch repair protein deficiency, particularly loss of PMS2 expression
Colin J R Stewart, Amy Pearn, Nicholas Pachter, et al.
Cardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology
|
May 21, 2018
A case of vascular Ehlers-Danlos Syndrome with a cardiomyopathy and multi-system involvement
Nick Si Rui Lan, Michael Fietz, Nicholas Pachter, et al.
International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society
|
May 19, 2019
Uptake of testing for germline <i>BRCA</i> mutations in patients with non-mucinous epithelial ovarian cancers in Western Australia: a comparison of different genetic counseling methods
Grace Stearnes, Cassandra B Nichols, Lyn Schofield, et al.
International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society
|
April 7, 2016
Impact of Clinical Genetics Attendance at a Gynecologic Oncology Tumor Board on Referrals for Genetic Counseling and BRCA Mutation Testing
Paul A Cohen, Cassandra B Nichols, Lyn Schofield, et al.
International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society
|
November 9, 2019
Incidence of germline BRCA1/2 mutations in women with tubo-ovarian high-grade serous carcinomas with and without serous tubal intra-epithelial carcinomas
Cassandra B Dowson, Colin Stewart, Sarah O'Sullivan, et al.
Asian Pacific Journal of Cancer Prevention : APJCP
|
October 29, 2021
Patient Satisfaction with Private Genetic Counselling for Familial Cancer in Western Australia: A Prospective Audit
Charmi N Perera, Sarah O'Sullivan, Nicholas Pachter, et al.
European Journal of Human Genetics : EJHG
|
November 26, 2024
Assessing the unmet needs of genomic testing in Australia: a geospatial exploration
Sarah Casauria, Felicity Collins, Susan M White, et al.
European Journal of Medical Genetics
|
August 18, 2020
Disclosing genetic information to family members without consent: Five Australian case studies
Jane Tiller, Gemma Bilkey, Rebecca Macintosh, et al.
Patient Education and Counseling
|
December 24, 2017
Investigating barriers to genetic counseling and germline mutation testing in women with suspected hereditary breast and ovarian cancer syndrome and Lynch syndrome
Josephine Shaw, Caroline Bulsara, Paul A Cohen, et al.
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of 6
Search research articles
Search
Showing results (1-10 of 56) with videos related to
Sort By:
Page
of 6
Plos One
|
December 30, 2011
An 11p15 imprinting centre region 2 deletion in a family with Beckwith Wiedemann syndrome provides insights into imprinting control at CDKN1C
Elizabeth Algar, Vinod Dagar, Menka Sebaj, et al.
Histopathology
|
May 1, 2018
Peritumoral granulomatous reaction in endometrial carcinoma: association with DNA mismatch repair protein deficiency, particularly loss of PMS2 expression
Colin J R Stewart, Amy Pearn, Nicholas Pachter, et al.
Cardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology
|
May 21, 2018
A case of vascular Ehlers-Danlos Syndrome with a cardiomyopathy and multi-system involvement
Nick Si Rui Lan, Michael Fietz, Nicholas Pachter, et al.
International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society
|
May 19, 2019
Uptake of testing for germline <i>BRCA</i> mutations in patients with non-mucinous epithelial ovarian cancers in Western Australia: a comparison of different genetic counseling methods
Grace Stearnes, Cassandra B Nichols, Lyn Schofield, et al.
International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society
|
April 7, 2016
Impact of Clinical Genetics Attendance at a Gynecologic Oncology Tumor Board on Referrals for Genetic Counseling and BRCA Mutation Testing
Paul A Cohen, Cassandra B Nichols, Lyn Schofield, et al.
International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society
|
November 9, 2019
Incidence of germline BRCA1/2 mutations in women with tubo-ovarian high-grade serous carcinomas with and without serous tubal intra-epithelial carcinomas
Cassandra B Dowson, Colin Stewart, Sarah O'Sullivan, et al.
Asian Pacific Journal of Cancer Prevention : APJCP
|
October 29, 2021
Patient Satisfaction with Private Genetic Counselling for Familial Cancer in Western Australia: A Prospective Audit
Charmi N Perera, Sarah O'Sullivan, Nicholas Pachter, et al.
European Journal of Human Genetics : EJHG
|
November 26, 2024
Assessing the unmet needs of genomic testing in Australia: a geospatial exploration
Sarah Casauria, Felicity Collins, Susan M White, et al.
European Journal of Medical Genetics
|
August 18, 2020
Disclosing genetic information to family members without consent: Five Australian case studies
Jane Tiller, Gemma Bilkey, Rebecca Macintosh, et al.
Patient Education and Counseling
|
December 24, 2017
Investigating barriers to genetic counseling and germline mutation testing in women with suspected hereditary breast and ovarian cancer syndrome and Lynch syndrome
Josephine Shaw, Caroline Bulsara, Paul A Cohen, et al.
Page
of 6