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BMC Medicine
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August 29, 2013
A novel serogenetic approach determines the community prevalence of celiac disease and informs improved diagnostic pathways
Robert P Anderson, Margaret J Henry, Roberta Taylor, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
February 24, 2023
Rare and Common Variants in GALNT3 May Affect Bone Mass Independently of Phosphate Metabolism
Neelam Hassan, Celia L Gregson, Haotian Tang, et al.
Bonekey Reports
|
February 7, 2014
Whole exome sequencing is an efficient, sensitive and specific method of mutation detection in osteogenesis imperfecta and Marfan syndrome
Aideen M McInerney-Leo, Mhairi S Marshall, Brooke Gardiner, et al.
Frontiers in Global Women'S Health
|
December 13, 2024
Healthcare providers' experiences of maternity care service delivery during the COVID-19 pandemic in the United Kingdom: a follow-up systematic review and qualitative evidence synthesis
Tisha Dasgupta, Emily Bousfield, Yosha Pathak, et al.
Frontiers in Reproductive Health
|
January 28, 2026
Seeking digital maternity healthcare during the pandemic health system shock: a systematic review of women's experiences in low- and middle-income countries
Tisha Dasgupta, Emily Russell, Camila Carbajal, et al.
Circulation. Genomic and Precision Medicine
|
March 21, 2018
A Screening Approach to Identify Clinically Actionable Variants Causing Congenital Heart Disease in Exome Data
Justin O Szot, Hartmut Cuny, Gillian M Blue, et al.
Pediatric Diabetes
|
September 8, 2018
Comprehensive genetic screening: The prevalence of maturity-onset diabetes of the young gene variants in a population-based childhood diabetes cohort
Stephanie R Johnson, Jonathan J Ellis, Paul J Leo, et al.
American Journal of Human Genetics
|
August 6, 2013
Short-rib polydactyly and Jeune syndromes are caused by mutations in WDR60
Aideen M McInerney-Leo, Miriam Schmidts, Claudio R Cortés, et al.
Eclinicalmedicine
|
December 7, 2021
Disentangling post-vaccination symptoms from early COVID-19
Liane S Canas, Marc F Österdahl, Jie Deng, et al.
American Journal of Human Genetics
|
March 6, 2012
Multicentric carpotarsal osteolysis is caused by mutations clustering in the amino-terminal transcriptional activation domain of MAFB
Andreas Zankl, Emma L Duncan, Paul J Leo, et al.
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of 14
Search research articles
Search
Showing results (71-80 of 138) with videos related to
Sort By:
Page
of 14
BMC Medicine
|
August 29, 2013
A novel serogenetic approach determines the community prevalence of celiac disease and informs improved diagnostic pathways
Robert P Anderson, Margaret J Henry, Roberta Taylor, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
February 24, 2023
Rare and Common Variants in GALNT3 May Affect Bone Mass Independently of Phosphate Metabolism
Neelam Hassan, Celia L Gregson, Haotian Tang, et al.
Bonekey Reports
|
February 7, 2014
Whole exome sequencing is an efficient, sensitive and specific method of mutation detection in osteogenesis imperfecta and Marfan syndrome
Aideen M McInerney-Leo, Mhairi S Marshall, Brooke Gardiner, et al.
Frontiers in Global Women'S Health
|
December 13, 2024
Healthcare providers' experiences of maternity care service delivery during the COVID-19 pandemic in the United Kingdom: a follow-up systematic review and qualitative evidence synthesis
Tisha Dasgupta, Emily Bousfield, Yosha Pathak, et al.
Frontiers in Reproductive Health
|
January 28, 2026
Seeking digital maternity healthcare during the pandemic health system shock: a systematic review of women's experiences in low- and middle-income countries
Tisha Dasgupta, Emily Russell, Camila Carbajal, et al.
Circulation. Genomic and Precision Medicine
|
March 21, 2018
A Screening Approach to Identify Clinically Actionable Variants Causing Congenital Heart Disease in Exome Data
Justin O Szot, Hartmut Cuny, Gillian M Blue, et al.
Pediatric Diabetes
|
September 8, 2018
Comprehensive genetic screening: The prevalence of maturity-onset diabetes of the young gene variants in a population-based childhood diabetes cohort
Stephanie R Johnson, Jonathan J Ellis, Paul J Leo, et al.
American Journal of Human Genetics
|
August 6, 2013
Short-rib polydactyly and Jeune syndromes are caused by mutations in WDR60
Aideen M McInerney-Leo, Miriam Schmidts, Claudio R Cortés, et al.
Eclinicalmedicine
|
December 7, 2021
Disentangling post-vaccination symptoms from early COVID-19
Liane S Canas, Marc F Österdahl, Jie Deng, et al.
American Journal of Human Genetics
|
March 6, 2012
Multicentric carpotarsal osteolysis is caused by mutations clustering in the amino-terminal transcriptional activation domain of MAFB
Andreas Zankl, Emma L Duncan, Paul J Leo, et al.
Page
of 14