Results 111 to 120 of about 17,432 (228)

Human diseases caused by homozygous PTH1R mutations. [PDF]

open access: yesFront Endocrinol (Lausanne)
Portales-Castillo I   +3 more
europepmc   +1 more source

Use of Artificial Intelligence-Based Software to Aid in the Identification of Ultrasound Findings Associated With Fetal Congenital Heart Defects. [PDF]

open access: yesObstet Gynecol
Lam-Rachlin J   +27 more
europepmc   +1 more source

Artificial Intelligence for the Detection of Fetal Ultrasound Findings Concerning for Major Congenital Heart Defects. [PDF]

open access: yesObstet Gynecol
Zelop CM   +23 more
europepmc   +1 more source

Recent Progress in Keloid Mechanism and Treatment: A Comprehensive Review. [PDF]

open access: yesBiomedicines
Merlino L   +6 more
europepmc   +1 more source

A mouse model of Jansen's metaphyseal chondrodysplasia for investigating disease mechanisms and candidate therapeutics. [PDF]

open access: yesProc Natl Acad Sci U S A
Höppner J   +16 more
europepmc   +1 more source

Gardella/exposing: the shop and the stand

open access: yesFestival dell'Architettura Magazine, 2018
Federico Marcolini
doaj   +1 more source

Assessing the Reliability of Hysteroscopic Sampling Methods for Diagnosing Atypical Endometrial Hyperplasia. [PDF]

open access: yesCancers (Basel)
Giannella L   +29 more
europepmc   +1 more source

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