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American Journal of Medical Genetics. Part A
|
April 21, 2004
3D analysis of facial morphology
Peter Hammond, Tim J Hutton, Judith E Allanson, et al.
American Journal of Human Genetics
|
May 7, 2002
PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity
Marco Tartaglia, Kamini Kalidas, Adam Shaw, et al.
Eclinicalmedicine
|
February 15, 2024
The comprehensive English National Lynch Syndrome Registry: development and description of a new genomics data resource
Catherine Huntley, Lucy Loong, Corinne Mallinson, et al.
Journal of Medical Genetics
|
August 16, 2015
Clinical and molecular predictors of mortality in neurofibromatosis 2: a UK national analysis of 1192 patients
Adam Hexter, Adrian Jones, Harry Joe, et al.
Journal of Medical Genetics
|
June 25, 2020
Sporadic vestibular schwannoma: a molecular testing summary
Katherine V Sadler, Naomi L Bowers, Claire Hartley, et al.
American Journal of Human Genetics
|
December 29, 2005
Discriminating power of localized three-dimensional facial morphology
Peter Hammond, Tim J Hutton, Judith E Allanson, et al.
Journal of Medical Genetics
|
October 21, 2024
Lynch syndrome diagnostic testing pathways in endometrial cancers: a nationwide English registry-based study
Lucy Loong, Catherine Huntley, Joanna Pethick, et al.
The Lancet. Gastroenterology & Hepatology
|
July 9, 2026
Aspirin for cancer prevention in individuals with Lynch syndrome: first results from the CaPP3 multicentre, randomised, double-blind, non-inferiority trial
John Burn, Gillian M Borthwick, Faye Elliott, et al.
Nature Medicine
|
May 2, 2018
Carboplatin in BRCA1/2-mutated and triple-negative breast cancer BRCAness subgroups: the TNT Trial
Andrew Tutt, Holly Tovey, Maggie Chon U Cheang, et al.
American Journal of Medical Genetics. Part A
|
September 21, 2016
Phenotype and genotype in 52 patients with Rubinstein-Taybi syndrome caused by EP300 mutations
Patricia Fergelot, Martine Van Belzen, Julien Van Gils, et al.
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of 4
Search research articles
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Showing results (31-40 of 40) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 40 results.
American Journal of Medical Genetics. Part A
|
April 21, 2004
3D analysis of facial morphology
Peter Hammond, Tim J Hutton, Judith E Allanson, et al.
American Journal of Human Genetics
|
May 7, 2002
PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity
Marco Tartaglia, Kamini Kalidas, Adam Shaw, et al.
Eclinicalmedicine
|
February 15, 2024
The comprehensive English National Lynch Syndrome Registry: development and description of a new genomics data resource
Catherine Huntley, Lucy Loong, Corinne Mallinson, et al.
Journal of Medical Genetics
|
August 16, 2015
Clinical and molecular predictors of mortality in neurofibromatosis 2: a UK national analysis of 1192 patients
Adam Hexter, Adrian Jones, Harry Joe, et al.
Journal of Medical Genetics
|
June 25, 2020
Sporadic vestibular schwannoma: a molecular testing summary
Katherine V Sadler, Naomi L Bowers, Claire Hartley, et al.
American Journal of Human Genetics
|
December 29, 2005
Discriminating power of localized three-dimensional facial morphology
Peter Hammond, Tim J Hutton, Judith E Allanson, et al.
Journal of Medical Genetics
|
October 21, 2024
Lynch syndrome diagnostic testing pathways in endometrial cancers: a nationwide English registry-based study
Lucy Loong, Catherine Huntley, Joanna Pethick, et al.
The Lancet. Gastroenterology & Hepatology
|
July 9, 2026
Aspirin for cancer prevention in individuals with Lynch syndrome: first results from the CaPP3 multicentre, randomised, double-blind, non-inferiority trial
John Burn, Gillian M Borthwick, Faye Elliott, et al.
Nature Medicine
|
May 2, 2018
Carboplatin in BRCA1/2-mutated and triple-negative breast cancer BRCAness subgroups: the TNT Trial
Andrew Tutt, Holly Tovey, Maggie Chon U Cheang, et al.
American Journal of Medical Genetics. Part A
|
September 21, 2016
Phenotype and genotype in 52 patients with Rubinstein-Taybi syndrome caused by EP300 mutations
Patricia Fergelot, Martine Van Belzen, Julien Van Gils, et al.
Page
of 4