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Human Molecular Genetics|September 16, 1998
Characterization of the myotubularin dual specificity phosphatase gene family from yeast to humanJ Laporte, F Blondeau, A Buj-Bello, et al.American Journal of Human Genetics|January 1, 1995
X-linked progressive mixed deafness: a new microdeletion that involves a more proximal region in Xq21C Piussan, A Hanauer, N Dahl, et al.ACS Biomaterials Science & Engineering|January 4, 2022
Promoting and Orienting Axon Extension Using Scaffold-Free Dental Pulp Stem Cell SheetsMichelle D Drewry, Matthew T Dailey, Kristi Rothermund, et al.Human Genetics|December 22, 1999
Truncating ribosomal protein S19 mutations and variable clinical expression in Diamond-Blackfan anemiaH Matsson, J Klar, N Draptchinskaia, et al.Genomics|June 14, 2000
Large-insert clone/STS contigs in Xq11-q12, spanning deletions in patients with androgen insensitivity and mental retardationM G Schueler, A W Higgins, R Nagaraja, et al.ERJ Open Research|March 5, 2025
Relationship between age, sex, geography and incidence of nontuberculous mycobacteria in Denmark from 1991 to 2022Victor N Dahl, Andreas A Pedersen, Jakko van Ingen, et al.Clinical Genetics|December 1, 1991
Genetic mapping of loci for X-linked retinitis pigmentosaN Dahl, M Sundvall, U Pettersson, et al.Human Molecular Genetics|April 1, 1995
Inversion of the IDS gene resulting from recombination with IDS-related sequences is a common cause of the Hunter syndromeM L Bondeson, N Dahl, H Malmgren, et al.Genomics|May 1, 1997
Cloning and characterization of an alternatively spliced gene in proximal Xq28 deleted in two patients with intersexual genitalia and myotubular myopathyJ Laporte, P Kioschis, L J Hu, et al.Human Genetics|September 15, 2000
Alpha-tectorin involvement in hearing disabilities: one gene--two phenotypesJ Balciuniene, N Dahl, P Jalonen, et al.Pageof 14