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The Journal of Clinical Investigation
|
July 24, 2018
Mosaic-variegated aneuploidy syndrome mutation or haploinsufficiency in Cep57 impairs tumor suppression
Khaled Aziz, Cynthia J Sieben, Karthik B Jeganathan, et al.
Journal of Health, Population, and Nutrition
|
November 15, 2014
Recognition of and Response to neonatal intrapartum-related complications in home-birth settings in Bangladesh
Kristin E VanderEnde, Allisyn C Moran, Karen Leasure, et al.
Current Topics in Medicinal Chemistry
|
April 27, 2022
Solanum pubescens Wild Fruits Essential Oil - A Golden Casket for its Antimicrobial and Anti-inflammatory Mediated Wound Healing Efficacy in Vertebrate Model Mus musculus
Haseebur Rahman, Nazneen Rahman, Mir Haris, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 10, 2010
Generation of trisomies in cancer cells by multipolar mitosis and incomplete cytokinesis
David Gisselsson, Yuesheng Jin, David Lindgren, et al.
Cancer Research
|
December 26, 2003
Evaluation of Fanconi Anemia genes in familial breast cancer predisposition
Sheila Seal, Rita Barfoot, Hiran Jayatilake, et al.
Human Mutation
|
March 14, 2013
Simple detection of germline microsatellite instability for diagnosis of constitutional mismatch repair cancer syndrome
Danielle Ingham, Christine P Diggle, Ian Berry, et al.
Breast Cancer Research and Treatment
|
June 1, 2010
Mutation and association analysis of GEN1 in breast cancer susceptibility
Clare Turnbull, Sarah Hines, Anthony Renwick, et al.
Scientific Reports
|
July 14, 2016
Implementing rapid, robust, cost-effective, patient-centred, routine genetic testing in ovarian cancer patients
Angela George, Daniel Riddell, Sheila Seal, et al.
American Journal of Medical Genetics. Part A
|
October 14, 2005
Familial gigantism caused by an NSD1 mutation
Mieke M van Haelst, Jeannette J M Hoogeboom, Genevieve Baujat, et al.
Human Molecular Genetics
|
May 15, 2015
Mutations in the PP2A regulatory subunit B family genes PPP2R5B, PPP2R5C and PPP2R5D cause human overgrowth
Chey Loveday, Katrina Tatton-Brown, Matthew Clarke, et al.
Page
of 16
Search research articles
Search
Showing results (51-60 of 154) with videos related to
Sort By:
Page
of 16
The Journal of Clinical Investigation
|
July 24, 2018
Mosaic-variegated aneuploidy syndrome mutation or haploinsufficiency in Cep57 impairs tumor suppression
Khaled Aziz, Cynthia J Sieben, Karthik B Jeganathan, et al.
Journal of Health, Population, and Nutrition
|
November 15, 2014
Recognition of and Response to neonatal intrapartum-related complications in home-birth settings in Bangladesh
Kristin E VanderEnde, Allisyn C Moran, Karen Leasure, et al.
Current Topics in Medicinal Chemistry
|
April 27, 2022
Solanum pubescens Wild Fruits Essential Oil - A Golden Casket for its Antimicrobial and Anti-inflammatory Mediated Wound Healing Efficacy in Vertebrate Model Mus musculus
Haseebur Rahman, Nazneen Rahman, Mir Haris, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 10, 2010
Generation of trisomies in cancer cells by multipolar mitosis and incomplete cytokinesis
David Gisselsson, Yuesheng Jin, David Lindgren, et al.
Cancer Research
|
December 26, 2003
Evaluation of Fanconi Anemia genes in familial breast cancer predisposition
Sheila Seal, Rita Barfoot, Hiran Jayatilake, et al.
Human Mutation
|
March 14, 2013
Simple detection of germline microsatellite instability for diagnosis of constitutional mismatch repair cancer syndrome
Danielle Ingham, Christine P Diggle, Ian Berry, et al.
Breast Cancer Research and Treatment
|
June 1, 2010
Mutation and association analysis of GEN1 in breast cancer susceptibility
Clare Turnbull, Sarah Hines, Anthony Renwick, et al.
Scientific Reports
|
July 14, 2016
Implementing rapid, robust, cost-effective, patient-centred, routine genetic testing in ovarian cancer patients
Angela George, Daniel Riddell, Sheila Seal, et al.
American Journal of Medical Genetics. Part A
|
October 14, 2005
Familial gigantism caused by an NSD1 mutation
Mieke M van Haelst, Jeannette J M Hoogeboom, Genevieve Baujat, et al.
Human Molecular Genetics
|
May 15, 2015
Mutations in the PP2A regulatory subunit B family genes PPP2R5B, PPP2R5C and PPP2R5D cause human overgrowth
Chey Loveday, Katrina Tatton-Brown, Matthew Clarke, et al.
Page
of 16