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Plos One
|
December 19, 2018
Late vertebral side effects in long-term survivors of irradiated childhood brain tumor
Miro-Pekka Jussila, Tiina Remes, Julia Anttonen, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
July 26, 2015
CXCR3 Polymorphism and Expression Associate with Spontaneous Preterm Birth
Minna K Karjalainen, Marja Ojaniemi, Antti M Haapalainen, et al.
Thyroid : Official Journal of the American Thyroid Association
|
July 5, 2016
Detection of Novel Gene Variants Associated with Congenital Hypothyroidism in a Finnish Patient Cohort
Christoffer Löf, Konrad Patyra, Teemu Kuulasmaa, et al.
JCI Insight
|
January 9, 2024
Mechanisms of thyrotropin receptor-mediated phenotype variability deciphered by gene mutations and M453T-knockin model
Kristiina Makkonen, Meeri Jännäri, Luís Crisóstomo, et al.
JCI Insight
|
October 19, 2018
Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism
Hakan Cangul, Xiao-Hui Liao, Erik Schoenmakers, et al.
Endocrine-Related Cancer
|
July 19, 2015
Clinical and genetic characterization of pituitary gigantism: an international collaborative study in 208 patients
Liliya Rostomyan, Adrian F Daly, Patrick Petrossians, et al.
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of 6
Search research articles
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Showing results (51-60 of 56) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 56 results.
Plos One
|
December 19, 2018
Late vertebral side effects in long-term survivors of irradiated childhood brain tumor
Miro-Pekka Jussila, Tiina Remes, Julia Anttonen, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
July 26, 2015
CXCR3 Polymorphism and Expression Associate with Spontaneous Preterm Birth
Minna K Karjalainen, Marja Ojaniemi, Antti M Haapalainen, et al.
Thyroid : Official Journal of the American Thyroid Association
|
July 5, 2016
Detection of Novel Gene Variants Associated with Congenital Hypothyroidism in a Finnish Patient Cohort
Christoffer Löf, Konrad Patyra, Teemu Kuulasmaa, et al.
JCI Insight
|
January 9, 2024
Mechanisms of thyrotropin receptor-mediated phenotype variability deciphered by gene mutations and M453T-knockin model
Kristiina Makkonen, Meeri Jännäri, Luís Crisóstomo, et al.
JCI Insight
|
October 19, 2018
Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism
Hakan Cangul, Xiao-Hui Liao, Erik Schoenmakers, et al.
Endocrine-Related Cancer
|
July 19, 2015
Clinical and genetic characterization of pituitary gigantism: an international collaborative study in 208 patients
Liliya Rostomyan, Adrian F Daly, Patrick Petrossians, et al.
Page
of 6