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Genomics|April 1, 1997
The XRCC2 DNA repair gene: identification of a positional candidateC E Tambini, A M George, J M Rommens, et al.European Journal of Human Genetics : EJHG|September 6, 2022
Developmental implications of genetic testing for physical indicationsDanielle A Baribeau, Ny Hoang, Thanuja Selvanayagam, et al.G3 (Bethesda, Md.)|November 7, 2013
Performance of high-throughput sequencing for the discovery of genetic variation across the complete size spectrumAndy Wing Chun Pang, Jeffrey R Macdonald, Ryan K C Yuen, et al.Ophthalmology. Retina|August 27, 2023
Terminology for Retinal Findings in Sickle Cell Disease Research: A Scoping ReviewGrace R Reilly, Yangyiran Xie, Roberta W Scherer, et al.The Journal of Chemical Physics|February 25, 2012
Electronic states and the influence of oxygen addition on the optical absorption behaviour of manganese phthalocyanineR Friedrich, T Hahn, J Kortus, et al.Molecular Genetics & Genomic Medicine|October 20, 2021
Predictors of empowerment in parents of children with autism and related neurodevelopmental disorders who are undergoing genetic testingIskra Peltekova, Afiqah Yusuf, Jennifer Frei, et al.Journal of Genetic Counseling|September 7, 2020
Adaptation and validation of the Genetic Counseling Outcome Scale for autism spectrum disorders and related conditionsAfiqah Yusuf, Iskra Peltekova, Tal Savion-Lemieux, et al.BMC Medical Genetics|May 8, 2020
Ancestry and frequency of genetic variants in the general population are confounders in the characterization of germline variants linked to cancerAnna Bobyn, Mehdi Zarrei, Yuankun Zhu, et al.Respiration Physiology|March 1, 1993
Microemboli reduce phase III slopes of CO2 and invert phase III slopes of infused SF6M S Schreiner, L G Leksell, S R Gobran, et al.Blood|May 1, 1996
Molecular definition of a narrow interval at 7q22.1 associated with myelodysplasiaE J Johnson, S W Scherer, L Osborne, et al.Pageof 88