Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Smith, Richard JH."'
Publikováno v:
In International Journal of Pediatric Otorhinolaryngology November 2021 150
Autor:
Benedek, Pálma, Balakrishnan, Karthik, Cunningham, Michael J., Friedman, Norman R., Goudy, Steven L., Ishman, Stacey L., Katona, Gábor, Kirkham, Erin M., Lam, Derek J., Leboulanger, Nicolas, Lee, Gi Soo, Le Treut, Claire, Mitchell, Ron B., Muntz, Harlan R., Musso, Mary Fances, Parikh, Sanjay R., Rahbar, Reza, Roy, Soham, Russell, John, Sidell, Douglas R., Sie, Kathleen C.Y., Smith, Richard JH., Soma, Marlene A., Wyatt, Michelle E., Zalzal, George, Zur, Karen B., Boudewyns, An
Publikováno v:
In International Journal of Pediatric Otorhinolaryngology November 2020 138
Autor:
Hildebrand, Michael S, Newton, Stephen S, Gubbels, Samuel P, Sheffield, Abraham M, Kochhar, Amit, de Silva, Michelle G, Dahl, Hans-Henrik M, Rose, Scott D, Behlke, Mark A, Smith, Richard JH
Publikováno v:
In Molecular Therapy February 2008 16(2):224-236
Publikováno v:
In The Lancet 2005 365(9462):879-890
Autor:
Shearer A Eliot, Hildebrand Michael S, Ravi Harini, Joshi Swati, Guiffre Angelica C, Novak Barbara, Happe Scott, LeProust Emily M, Smith Richard JH
Publikováno v:
BMC Genomics, Vol 13, Iss 1, p 618 (2012)
Abstract Background Targeted genomic enrichment (TGE) is a widely used method for isolating and enriching specific genomic regions prior to massively parallel sequencing. To make effective use of sequencer output, barcoding and sample pooling (multip
Externí odkaz:
https://doaj.org/article/56f45441d56945659b27e42c21cd6038
Publikováno v:
BMC Biotechnology, Vol 12, Iss 1, p 20 (2012)
Abstract Background Solution-based targeted genomic enrichment (TGE) protocols permit selective sequencing of genomic regions of interest on a massively parallel scale. These protocols could be improved by: 1) modifying or eliminating time consuming
Externí odkaz:
https://doaj.org/article/2320a0b8a6a04b8a8ff4181d5aa17f17
Autor:
Smith Richard JH, Pollak Martin R, Meyer Nicole, Cheng Junsheng, Hao Ke, Leykin Igor, Wong Wing, Rosenow Carsten, Li Cheng
Publikováno v:
BMC Genetics, Vol 6, Iss 1, p 7 (2005)
Abstract Background The identification of disease-associated genes using single nucleotide polymorphisms (SNPs) has been increasingly reported. In particular, the Affymetrix Mapping 10 K SNP microarray platform uses one PCR primer to amplify the DNA
Externí odkaz:
https://doaj.org/article/8789a84c3e55413c83d70694af07a058
Autor:
Kemerley, Andrew, Sloan-Heggen, Christina M, Pfeifer, Wanda L, Smith, Richard JH, Drack, Arlene V
Baraitser-Winter syndrome (cerebrofrontofacial syndrome, type 3) is a rare developmental disorder typified by hypertelorism, ptosis, high-arched eyebrows, ocular coloboma, and brain malformations. Other common manifestations include hearing loss, sho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3f6853dac1eb518a6d26a6c4960d70cd
https://europepmc.org/articles/PMC5722223/
https://europepmc.org/articles/PMC5722223/
Publikováno v:
Journal of Medical Genetics (JMG); 2018, Vol. 55 Issue: 8 p555-560, 6p
Publikováno v:
Current Opinion in Otolaryngology & Head & Neck Surgery; 2011 Oct, Vol. 19 Issue 5, p397-402, 6p