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Saudi Medical Journal|July 28, 2005
Homozygous AMN mutation in hereditary selective intestinal malabsorption of vitamin B12 in JordanJamil R Al-Alami, Stephan M Tanner, Marwan K Tayeh, et al.European Journal of Cancer & Clinical Oncology|July 1, 1988
Immunoglobulin kappa and lambda light chain dual genotype rearrangement in a patient with kappa-secreting B-CLLP Peltomäki, N O Bianchi, S Knuutila, et al.European Journal of Human Genetics : EJHG|February 13, 2014
Biallelic MUTYH mutations can mimic Lynch syndromeMonika Morak, Barbara Heidenreich, Gisela Keller, et al.Journal of the National Cancer Institute|February 14, 2008
The frequency of Muir-Torre syndrome among Lynch syndrome familiesChristopher D South, Heather Hampel, Ilene Comeras, et al.Infectious Diseases Now|December 13, 2021
Implementation of point-of-care ultrasonography in an infectious disease wardCharles Declerck, Rafael Mahieu, Diane Sanderink, et al.Geriatrie Et Psychologie Neuropsychiatrie Du Vieillissement|November 19, 2021
[Theory of mind, empathy and eye gaze strategies during an artwork observation in neurodegenerative pathologies]Kevin Polet, Solange Hesse, Adeline Morisot, et al.British Journal of Cancer|September 9, 2004
MSH6 missense mutations are often associated with no or low cancer susceptibilityR Kariola, H Hampel, W L Frankel, et al.Human Molecular Genetics|January 1, 1995
Assignment of an Usher syndrome type III (USH3) gene to chromosome 3qE M Sankila, L Pakarinen, H Kääriäinen, et al.Thyroid : Official Journal of the American Thyroid Association|April 10, 2004
CITED1 protein expression suggests Papillary Thyroid Carcinoma in high throughput tissue microarray-based studyManju L Prasad, Natalia S Pellegata, Richard T Kloos, et al.Proceedings of the National Academy of Sciences of the United States of America|May 1, 1991
Localization of a gene for progressive myoclonus epilepsy to chromosome 21q22A E Lehesjoki, M Koskiniemi, P Sistonen, et al.Pageof 61