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Current Genetic Medicine Reports
|
October 10, 2022
Genodermatoses - Opportunities for Early Detection and Cancer Prevention
Helena Carley, Anjana Kulkarni
Best Practice & Research. Clinical Obstetrics & Gynaecology
|
July 10, 2024
Reproductive decision-making in cancer susceptibility syndromes
Helena Carley, Anjana Kulkarni
BJOG : an International Journal of Obstetrics and Gynaecology
|
July 23, 2021
Prenatal diagnosis and pre-implantation genetic diagnosis for cancer susceptibility conditions
Anjana Kulkarni, Mark David Kilby
BJOG : an International Journal of Obstetrics and Gynaecology
|
June 19, 2023
Prenatal and pre-implantation genetic testing for monogenic disorders for germline cancer susceptibility gene variants: UK joint consensus guidance
Mohamed Wafik, Mark David Kilby, Anjana Kulkarni, et al.
JEADV Clinical Practice
|
September 9, 2024
Identification and functional validation of a novel pathogenic <i>POT1</i> germline variant p.G95V in familial melanoma
Farrah Bakr, Anjana Kulkarni, Stephen Mounsey, et al.
Journal of Medical Genetics
|
April 26, 2019
Structural Aberrations with Secondary Implications (SASIs): consensus recommendations for reporting of cancer susceptibility genes identified during analysis of Copy Number Variants (CNVs)
Sabrina Talukdar, Lara Hawkes, Helen Hanson, et al.
American Journal of Medical Genetics. Part A
|
November 23, 2011
Vestibular schwannomas occur in schwannomatosis and should not be considered an exclusion criterion for clinical diagnosis
Miriam J Smith, Anjana Kulkarni, Cecilie Rustad, et al.
ESMO Open
|
June 28, 2019
Prospective analysis of 895 patients on a UK Genomics Review Board
David Allan Moore, Marina Kushnir, Gabriel Mak, et al.
Aging Cell
|
October 18, 2024
Multiple outcomes of the germline p16<sup>INK4a</sup> mutation affecting senescence and immunity in human skin
Priya Subramanian, Souraya Sayegh, Phatthamon Laphanuwat, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 3, 2022
Reclassification of clinically-detected sequence variants: Framework for genetic clinicians and clinical scientists by CanVIG-UK (Cancer Variant Interpretation Group UK)
Lucy Loong, Alice Garrett, Sophie Allen, et al.
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of 2
Search research articles
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Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
Current Genetic Medicine Reports
|
October 10, 2022
Genodermatoses - Opportunities for Early Detection and Cancer Prevention
Helena Carley, Anjana Kulkarni
Best Practice & Research. Clinical Obstetrics & Gynaecology
|
July 10, 2024
Reproductive decision-making in cancer susceptibility syndromes
Helena Carley, Anjana Kulkarni
BJOG : an International Journal of Obstetrics and Gynaecology
|
July 23, 2021
Prenatal diagnosis and pre-implantation genetic diagnosis for cancer susceptibility conditions
Anjana Kulkarni, Mark David Kilby
BJOG : an International Journal of Obstetrics and Gynaecology
|
June 19, 2023
Prenatal and pre-implantation genetic testing for monogenic disorders for germline cancer susceptibility gene variants: UK joint consensus guidance
Mohamed Wafik, Mark David Kilby, Anjana Kulkarni, et al.
JEADV Clinical Practice
|
September 9, 2024
Identification and functional validation of a novel pathogenic <i>POT1</i> germline variant p.G95V in familial melanoma
Farrah Bakr, Anjana Kulkarni, Stephen Mounsey, et al.
Journal of Medical Genetics
|
April 26, 2019
Structural Aberrations with Secondary Implications (SASIs): consensus recommendations for reporting of cancer susceptibility genes identified during analysis of Copy Number Variants (CNVs)
Sabrina Talukdar, Lara Hawkes, Helen Hanson, et al.
American Journal of Medical Genetics. Part A
|
November 23, 2011
Vestibular schwannomas occur in schwannomatosis and should not be considered an exclusion criterion for clinical diagnosis
Miriam J Smith, Anjana Kulkarni, Cecilie Rustad, et al.
ESMO Open
|
June 28, 2019
Prospective analysis of 895 patients on a UK Genomics Review Board
David Allan Moore, Marina Kushnir, Gabriel Mak, et al.
Aging Cell
|
October 18, 2024
Multiple outcomes of the germline p16<sup>INK4a</sup> mutation affecting senescence and immunity in human skin
Priya Subramanian, Souraya Sayegh, Phatthamon Laphanuwat, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 3, 2022
Reclassification of clinically-detected sequence variants: Framework for genetic clinicians and clinical scientists by CanVIG-UK (Cancer Variant Interpretation Group UK)
Lucy Loong, Alice Garrett, Sophie Allen, et al.
Page
of 2