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Journal of Medical Genetics|October 9, 2012
Co-occurrence of recurrent duplications of the DiGeorge syndrome region on both chromosome 22 homologues due to inherited and de novo eventsWeimin Bi, Frank J Probst, Joanna Wiszniewska, et al.
Neurogenetics|August 15, 2012
Small genomic rearrangements involving FMR1 support the importance of its gene dosage for normal neurocognitive functionSandesh C S Nagamani, Ayelet Erez, Frank J Probst, et al.
ISME Communications|April 4, 2025
Inferring replication states of bacteria and viruses in enrichment cultures via long-read sequencingSophie A Simon, André R Soares, Till L V Bornemann, et al.
Science (New York, N.Y.)|June 20, 1998
Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3A Wang, Y Liang, R A Fridell, et al.
Science (New York, N.Y.)|June 20, 1998
Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgeneF J Probst, R A Fridell, Y Raphael, et al.
Frontiers in Microbiology|June 25, 2015
S-layers at second glance? Altiarchaeal grappling hooks (hami) resemble archaeal S-layer proteins in structure and sequenceAlexandra K Perras, Bertram Daum, Christine Ziegler, et al.
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