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Journal of the Endocrine Society
|
January 6, 2022
Adrenal Incidentaloma: Prevalence and Referral Patterns From Routine Practice in a Large UK University Teaching Hospital
Fahmy W F Hanna, Sarah Hancock, Cherian George, et al.
Epigenomics
|
February 19, 2013
Combined influence of gene-specific cord blood methylation and maternal smoking habit on birth weight
Kim E Haworth, William E Farrell, Richard D Emes, et al.
Epigenetics
|
March 2, 2016
Quantitative genome-wide methylation analysis of high-grade non-muscle invasive bladder cancer
Mark O Kitchen, Richard T Bryan, Richard D Emes, et al.
Journal of Neurology
|
May 26, 2001
HLA-DRB1 and disease outcome in multiple sclerosis
S J Weatherby, W Thomson, L Pepper, et al.
The Journal of Investigative Dermatology
|
August 12, 1998
Susceptibility to melanoma: influence of skin type and polymorphism in the melanocyte stimulating hormone receptor gene
F Ichii-Jones, J T Lear, A H Heagerty, et al.
Nature Genetics
|
November 5, 1997
Mutations in transcriptional regulator ATRX establish the functional significance of a PHD-like domain
R J Gibbons, S Bachoo, D J Picketts, et al.
Leukemia
|
February 1, 2014
Single-cell genetic analysis reveals the composition of initiating clones and phylogenetic patterns of branching and parallel evolution in myeloma
L Melchor, A Brioli, C P Wardell, et al.
Diabetes Therapy : Research, Treatment and Education of Diabetes and Related Disorders
|
February 22, 2023
The Effect of the COVID-19 Pandemic on HbA1c Testing: Prioritization of High-Risk Cases and Impact of Social Deprivation
David Holland, Adrian H Heald, Fahmy F W Hanna, et al.
Journal of Medical Genetics
|
September 13, 2005
The phenotypic spectrum in patients with arginine to cysteine mutations in the COL2A1 gene
K P Hoornaert, C Dewinter, I Vereecke, et al.
Human Molecular Genetics
|
November 13, 1998
Multilocus linkage identifies two new loci for a mendelian form of stroke, cerebral cavernous malformation, at 7p15-13 and 3q25.2-27
H D Craig, M Günel, O Cepeda, et al.
Page
of 38
Search research articles
Search
Showing results (361-370 of 378) with videos related to
Sort By:
Page
of 38
Journal of the Endocrine Society
|
January 6, 2022
Adrenal Incidentaloma: Prevalence and Referral Patterns From Routine Practice in a Large UK University Teaching Hospital
Fahmy W F Hanna, Sarah Hancock, Cherian George, et al.
Epigenomics
|
February 19, 2013
Combined influence of gene-specific cord blood methylation and maternal smoking habit on birth weight
Kim E Haworth, William E Farrell, Richard D Emes, et al.
Epigenetics
|
March 2, 2016
Quantitative genome-wide methylation analysis of high-grade non-muscle invasive bladder cancer
Mark O Kitchen, Richard T Bryan, Richard D Emes, et al.
Journal of Neurology
|
May 26, 2001
HLA-DRB1 and disease outcome in multiple sclerosis
S J Weatherby, W Thomson, L Pepper, et al.
The Journal of Investigative Dermatology
|
August 12, 1998
Susceptibility to melanoma: influence of skin type and polymorphism in the melanocyte stimulating hormone receptor gene
F Ichii-Jones, J T Lear, A H Heagerty, et al.
Nature Genetics
|
November 5, 1997
Mutations in transcriptional regulator ATRX establish the functional significance of a PHD-like domain
R J Gibbons, S Bachoo, D J Picketts, et al.
Leukemia
|
February 1, 2014
Single-cell genetic analysis reveals the composition of initiating clones and phylogenetic patterns of branching and parallel evolution in myeloma
L Melchor, A Brioli, C P Wardell, et al.
Diabetes Therapy : Research, Treatment and Education of Diabetes and Related Disorders
|
February 22, 2023
The Effect of the COVID-19 Pandemic on HbA1c Testing: Prioritization of High-Risk Cases and Impact of Social Deprivation
David Holland, Adrian H Heald, Fahmy F W Hanna, et al.
Journal of Medical Genetics
|
September 13, 2005
The phenotypic spectrum in patients with arginine to cysteine mutations in the COL2A1 gene
K P Hoornaert, C Dewinter, I Vereecke, et al.
Human Molecular Genetics
|
November 13, 1998
Multilocus linkage identifies two new loci for a mendelian form of stroke, cerebral cavernous malformation, at 7p15-13 and 3q25.2-27
H D Craig, M Günel, O Cepeda, et al.
Page
of 38