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Human Molecular Genetics|March 1, 1997
Molecular and phenotypic variation in patients with severe Hunter syndromeK M Timms, M L Bondeson, M A Ansari-Lari, et al.
Journal of Medical Genetics|May 6, 2008
Noonan and cardio-facio-cutaneous syndromes: two clinically and genetically overlapping disordersA-M Nyström, S Ekvall, E Berglund, et al.
Genes, Chromosomes & Cancer|May 23, 1998
Cytogenetic comparison of primary tumors and lymph node metastases in breast cancer patientsN Pandis, M R Teixeira, A Adeyinka, et al.
Annals of Human Genetics|February 3, 2009
Candidate gene association study for noise-induced hearing loss in two independent noise-exposed populationsA Konings, L Van Laer, A Wiktorek-Smagur, et al.
Molecular Psychiatry|February 4, 2015
X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genesH Hu, S A Haas, J Chelly, et al.
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