Search research articles
Contact Us
Filters
Showing results (271-280 of 276) with videos related to
Page
of 28
Sort By:
You have reached the last page of results.
This site can display upto 276 results.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme
|
April 15, 2010
A European evidence-based guideline for the prevention of type 2 diabetes
B Paulweber, P Valensi, J Lindström, et al.
Nature Communications
|
July 11, 2023
Gain and loss of function variants in EZH1 disrupt neurogenesis and cause dominant and recessive neurodevelopmental disorders
Carolina Gracia-Diaz, Yijing Zhou, Qian Yang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 9, 2022
Genomic and phenotypic characterization of 404 individuals with neurodevelopmental disorders caused by CTNNB1 variants
Sayaka Kayumi, Luis A Pérez-Jurado, María Palomares, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme
|
April 15, 2010
Quality indicators for the prevention of type 2 diabetes in Europe--IMAGE
P Pajunen, R Landgraf, F Muylle, et al.
American Journal of Medical Genetics. Part A
|
March 30, 2021
Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann-Steiner syndrome
Sarah E Sheppard, Ian M Campbell, Margaret H Harr, et al.
Science Advances
|
March 10, 2023
Mechanism of KMT5B haploinsufficiency in neurodevelopment in humans and mice
Sarah E Sheppard, Laura Bryant, Rochelle N Wickramasekara, et al.
Page
of 28
Search research articles
Search
Showing results (271-280 of 276) with videos related to
Sort By:
Page
of 28
You have reached the last page of results.
This site can display upto 276 results.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme
|
April 15, 2010
A European evidence-based guideline for the prevention of type 2 diabetes
B Paulweber, P Valensi, J Lindström, et al.
Nature Communications
|
July 11, 2023
Gain and loss of function variants in EZH1 disrupt neurogenesis and cause dominant and recessive neurodevelopmental disorders
Carolina Gracia-Diaz, Yijing Zhou, Qian Yang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 9, 2022
Genomic and phenotypic characterization of 404 individuals with neurodevelopmental disorders caused by CTNNB1 variants
Sayaka Kayumi, Luis A Pérez-Jurado, María Palomares, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme
|
April 15, 2010
Quality indicators for the prevention of type 2 diabetes in Europe--IMAGE
P Pajunen, R Landgraf, F Muylle, et al.
American Journal of Medical Genetics. Part A
|
March 30, 2021
Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann-Steiner syndrome
Sarah E Sheppard, Ian M Campbell, Margaret H Harr, et al.
Science Advances
|
March 10, 2023
Mechanism of KMT5B haploinsufficiency in neurodevelopment in humans and mice
Sarah E Sheppard, Laura Bryant, Rochelle N Wickramasekara, et al.
Page
of 28