Results 101 to 110 of about 2,971 (153)

Mexican Patients With Suspected 22q11.2 Deletion Syndrome: Clinical Characterization and Molecular Findings by Fluorescence In Situ Hybridization and Multiplex Ligation-Dependent Probe Amplification. [PDF]

open access: yesMol Genet Genomic Med
Aguayo-Orozco TA   +7 more
europepmc   +1 more source

Metabolomic and transcriptomic landscape of the bovine uterine lumen during the second week of the estrous cycle. [PDF]

open access: yesJ Anim Sci Biotechnol
Waheed A   +8 more
europepmc   +1 more source

Consensus-based detection of aetiologic copy number variants for syndromic orofacial clefts utilising whole exome sequencing of case parent trios. [PDF]

open access: yesBMC Genom Data
Quaynor SK   +9 more
europepmc   +1 more source

Home - About - Disclaimer - Privacy