FRITZ SEDLAZECK to Neurodevelopmental Disorders
This is a "connection" page, showing publications FRITZ SEDLAZECK has written about Neurodevelopmental Disorders.
Connection Strength
0.278
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Long read sequencing and expression studies of AHDC1 deletions in Xia-Gibbs syndrome reveal a novel genetic regulatory mechanism. Hum Mutat. 2022 12; 43(12):2033-2053.
Score: 0.143
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Ultrarapid Nanopore Genome Sequencing in a Critical Care Setting. N Engl J Med. 2022 02 17; 386(7):700-702.
Score: 0.136