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Human Genetics|February 14, 2006
Association between the MLH1 gene and longevityDong Jo Kim, Sang Mi Yi, Seung Yeon Lee, et al.Human Genetics|January 21, 2006
Inactivation status of PCDH11X: sexual dimorphisms in gene expression levels in brainAlexandra M Lopes, Norman Ross, James Close, et al.Human Genetics|January 13, 2006
A SALL4 zinc finger missense mutation predicted to result in increased DNA binding affinity is associated with cranial midline defects and mild features of Okihiro syndromeJan Miertus, Wiktor Borozdin, Vladimir Frecer, et al.Human Genetics|January 28, 1999
Genomic structure of the human ezrin geneP Majander-Nordenswan, M Sainio, O Turunen, et al.Human Genetics|January 28, 1999
Characterization of mutations in patients with autoimmune polyglandular syndrome type 1 (APS1)C Y Wang, A Davoodi-Semiromi, W Huang, et al.Human Genetics|January 28, 1999
Relaxation of imprinting in Prader-Willi syndromeP K Rogan, J R Seip, L M White, et al.Human Genetics|January 28, 1999
Chromosomal fragile site expression in lymphocytes from patients with schizophreniaC H Chen, H H Shih, S Wang-Wuu, et al.Human Genetics|January 28, 1999
Complete mutational screening of the CFTR gene in 120 patients with pulmonary diseaseC Bombieri, M Benetazzo, A Saccomani, et al.Human Genetics|November 3, 1998
The molecular genetics of growth hormone deficiencyA M Procter, J A Phillips, D N CooperHuman Genetics|November 3, 1998
A functional polymorphism in the monoamine oxidase A gene promoterS Z Sabol, S Hu, D HamerPageof 957