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American Journal of Medical Genetics. Part A|June 9, 2006
Mosaicism for a full mutation, premutation, and deletion of the CGG repeats results in 22% FMRP and elevated FMR1 mRNA levels in a high-functioning fragile X maleXiao-Dong Han, Berkley R Powell, Judith L Phalin, et al.Journal De Chirurgie|June 16, 2009
[Primary leiomyosarcoma of the pancreas]S Rifki Jai, F Bensardi, A Hizaz, et al.American Journal of Human Genetics|February 1, 1991
A dimorphic 4-bp repeat in the cystic fibrosis gene is in absolute linkage disequilibrium with the delta F508 mutation: implications for prenatal diagnosis and mutation originF F Chehab, J Johnson, E Louie, et al.Plos One|September 19, 2014
First report of a deletion encompassing an entire exon in the homogentisate 1,2-dioxygenase gene causing alkaptonuriaMohammad Zouheir Habbal, Tarek Bou-Assi, Jun Zhu, et al.FEBS Letters|April 23, 2003
Comparison of the anti-apoptotic effects of Bcr-Abl, Bcl-2 and Bcl-x(L) following diverse apoptogenic stimuliGabriela Brumatti, Ricardo Weinlich, Cristina F Chehab, et al.Journal De Pharmacie De Belgique|October 4, 2018
[Evaluation of preoperative nutritional status in visceral surgery Correlational study]H El Alama, R Boufettal, A Benmoussa, et al.Preventive Medicine|May 23, 2026
Prevalence and associated social determinants of health for pregestational and gestational diabetes mellitus in California by disaggregated racial and ethnic groups and subgroupsCheng-Tzu Hsieh, Xinze Xu, Xuyuehe Ren, et al.BJOG : an International Journal of Obstetrics and Gynaecology|March 8, 2026
Maternal Obesity, Gestational Diabetes Mellitus and Offspring's Body Mass Index Trajectories From Birth to Age 6 Years: Glucose in Relation to Women and Babies' Health (GrownB) StudyCheng-Tzu Hsieh, Xinyue Liu, Xiang Li, et al.The American Statistician|October 10, 2024
Prioritizing Variables for Observational Study Design using the Joint Variable Importance PlotLauren D Liao, Yeyi Zhu, Amanda L Ngo, et al.Blood|January 1, 1993
Rapid and simultaneous typing of hemoglobin S, hemoglobin C, and seven Mediterranean beta-thalassemia mutations by covalent reverse dot-blot analysis: application to prenatal diagnosis in SicilyA Maggio, A Giambona, S P Cai, et al.Pageof 10