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Annals of Hematology|September 1, 2005
Genomewide linkage analysis of soluble transferrin receptor plasma levelsAngel F Remacha, Joan C Souto, José Manuel Soria, et al.
European Journal of Human Genetics : EJHG|April 26, 2002
DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34Mirna Mustapha, Eliane Chouery, Sébastien Chardenoux, et al.
Frontiers in Reproductive Health|June 7, 2023
Equipping providers to offer novel MPTs: Developing counseling messages for the Dual Prevention Pill in clinical studies and beyondKate Segal, Danielle M Harris, Andy Carmone, et al.
Human Genetics|December 17, 2002
A novel locus for autosomal dominant nonsyndromic hearing loss (DFNA44) maps to chromosome 3q28-29Silvia Modamio-Høybjør, Miguel Angel Moreno-Pelayo, Angeles Mencía, et al.
Journal of Human Genetics|July 8, 2011
A polymorphism of the POLG2 gene is genetically associated with the invasiveness of urinary bladder cancer in Japanese malesChanavee Ratanajaraya, Hiroyuki Nishiyama, Meiko Takahashi, et al.
Investigative Ophthalmology & Visual Science|May 20, 2026
Comparative Analysis of Intravitreal Diffusion Patterns Across Ex Vivo Human and In Vivo/Ex Vivo Animal ModelsAnfisa Ayalon, Avigail Beryozkin, Katherine A Davoli, et al.
Journal of Human Genetics|July 9, 2024
Genomic variants associated with age at diagnosis of childhood-onset type 1 diabetesPierre Bougnères, Sophie Le Fur, Yoichiro Kamatani, et al.
American Journal of Human Genetics|December 1, 1986
Further linkage data on cystic fibrosis: the Utah StudyR White, M Leppert, P O'Connell, et al.
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