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Circulation. Genomic and Precision Medicine|February 21, 2023
Evidence-Based Assessment of Congenital Heart Disease Genes to Enable Returning Results in a Genomic StudyEmily L Griffin, Shannon N Nees, Sarah U Morton, et al.American Journal of Respiratory and Critical Care Medicine|October 13, 2018
Bone Morphogenetic Protein 9 Is a Mechanistic Biomarker of Portopulmonary HypertensionIvana Nikolic, Lai-Ming Yung, Peiran Yang, et al.American Journal of Obstetrics and Gynecology|February 4, 2020
Micronized vaginal progesterone to prevent miscarriage: a critical evaluation of randomized evidenceArri Coomarasamy, Adam J Devall, Jan J Brosens, et al.Nature Genetics|December 8, 2009
A restricted spectrum of NRAS mutations causes Noonan syndromeIon C Cirstea, Kerstin Kutsche, Radovan Dvorsky, et al.Nature Astronomy|April 25, 2023
Neutron star mass estimates from gamma-ray eclipses in spider millisecond pulsar binariesC J Clark, M Kerr, E D Barr, et al.JAMA Network Open|August 8, 2025
Sex-Related Measurement Bias in Autism Spectrum Disorder Symptoms in the Baby Siblings Research ConsortiumCatherine A Burrows, Sooyeon Sung, Shuting Zheng, et al.Human Genetics|January 9, 2016
Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndromeElisabeth E Mlynarski, Michael Xie, Deanne Taylor, et al.Brain : a Journal of Neurology|February 11, 2020
Clinical, morphological and genetic characterization of Brody disease: an international study of 40 patientsJoery P Molenaar, Jamie I Verhoeven, Richard J Rodenburg, et al.Annals of the Rheumatic Diseases|January 27, 2017
Cytosolic 5'-nucleotidase 1A autoantibody profile and clinical characteristics in inclusion body myositisJ B Lilleker, A Rietveld, S R Pye, et al.Circulation. Genomic and Precision Medicine|August 20, 2020
De Novo Damaging Variants, Clinical Phenotypes, and Post-Operative Outcomes in Congenital Heart DiseaseMarko T Boskovski, Jason Homsy, Meena Nathan, et al.Pageof 236