المؤلفون: Cremers, Frans PM, Kimberling, William J, Külm, Maigi, de Brouwer, Arjan P, van Wijk, Erwin, te Brinke, Heleen, Cremers, Cor WRJ, Hoefsloot, Lies H, Banfi, Sandro, Simonelli, Francesca, Fleischhauer, Johannes C, Berger, Wolfgang, Kelley, Phil M, Haralambous, Elene, Bitner-Glindzicz, Maria, Webster, Andrew R, Saihan, Zubin, De Baere, Elfride, Leroy, Bart, Silvestri, Giuliana, McKay, Gareth J, Koenekoop, Robert K, Millan, Jose M, Rosenberg, Thomas, Joensuu, Tarja, Sankila, Eeva-Marja, Weil, Dominique, Weston, Mike D, Wissinger, Bernd, Kremer, Hannie

المصدر: JOURNAL OF MEDICAL GENETICS ; ISSN: 0022-2593

مصطلحات موضوعية: Medicine and Health Sciences, ARRAYED PRIMER EXTENSION, SYNDROME-TYPE-II, LEBER CONGENITAL AMAUROSIS, MYOSIN VIIA GENE, RECESSIVE RETINITIS-PIGMENTOSA, EAR SENSORY CELLS, SYNDROME TYPE 1F, MUTATION DETECTION, HEARING-LOSS, USH2A GENE

وصف الملف: application/pdf

Relation: https://biblio.ugent.be/publication/369918; http://hdl.handle.net/1854/LU-369918; http://dx.doi.org/10.1136/jmg.2006.044784; https://biblio.ugent.be/publication/369918/file/6796456

الاتاحة: https://biblio.ugent.be/publication/369918
http://hdl.handle.net/1854/LU-369918
https://doi.org/10.1136/jmg.2006.044784
https://biblio.ugent.be/publication/369918/file/6796456

المؤلفون: Kelley, Philip M., Weston, Mike D., Chen, Zheng-Yi, Orten, Dana J., Hasson, Tama, Overbeck, Larry D., Pinnt, Jeff, Talmadge, Catherine B., Ing, Paul, Mooseker, Mark S., Corey, David, Sumegi, Janos, Kimberling, William J.

المصدر: Genomics ; volume 40, issue 1, page 73-79 ; ISSN 0888-7543

الاتاحة: http://dx.doi.org/10.1006/geno.1996.4545
https://api.elsevier.com/content/article/PII:S0888754396945450?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0888754396945450?httpAccept=text/plain

المؤلفون: Cremers, Frans P M, Kimberling, William J, Külm, Maigi, de Brouwer, Arjan P, van Wijk, Erwin, te Brinke, Heleen, Cremers, Cor W R J, Hoefsloot, Lies H, Banfi, Sandro, Simonelli, Francesca, Fleischhauer, Johannes C, Berger, Wolfgang, Kelley, Phil M, Haralambous, Elene, Bitner-Glindzicz, Maria, Webster, Andrew R, Saihan, Zubin, De Baere, Elfride, Leroy, Bart P, Silvestri, Giuliana, McKay, Gareth J, Koenekoop, Robert K, Millan, Jose M, Rosenberg, Thomas, Joensuu, Tarja, Sankila, Eeva-Marja, Weil, Dominique, Weston, Mike D, Wissinger, Bernd, Kremer, Hannie

المصدر: Cremers, Frans P M; Kimberling, William J; Külm, Maigi; de Brouwer, Arjan P; van Wijk, Erwin; te Brinke, Heleen; Cremers, Cor W R J; Hoefsloot, Lies H; Banfi, Sandro; Simonelli, Francesca; Fleischhauer, Johannes C; Berger, Wolfgang; Kelley, Phil M; Haralambous, Elene; Bitner-Glindzicz, Maria; Webster, Andrew R; Saihan, Zubin; De Baere, Elfride; Leroy, Bart P; Silvestri, Giuliana; . (2007). Development of a genotyping microarray for Usher syndrome. Journal of medical genetics, 44(2), pp. 153-60. London: BMJ Publishing Group 10.1136/jmg.2006.044784

Relation: https://boris.unibe.ch/20445/

الاتاحة: https://boris.unibe.ch/20445/

المؤلفون: Usami, Shin-ichi, Abe, Satoko, Weston, Mike D., Shinkawa, Hideichi, Van Camp, Guy, Kimberling, William J.

المصدر: 0340-6717 ; Human genetics

Relation: info:eu-repo/semantics/altIdentifier/isi/000079276900011

الاتاحة: https://hdl.handle.net/10067/238420151162165141

المؤلفون: Usami, S., Abe, Satoko, Weston, Mike D., Shinkawa, Hideichi, Van Camp, Guy, Kimberling, William J.

المصدر: Human Genetics ; volume 104, issue 2, page 188-192 ; ISSN 0340-6717 1432-1203

الاتاحة: http://dx.doi.org/10.1007/s004390050933
http://link.springer.com/content/pdf/10.1007/s004390050933.pdf
http://link.springer.com/article/10.1007/s004390050933/fulltext.html
http://link.springer.com/content/pdf/10.1007/s004390050933

المؤلفون: Abe, Satoko, Usami, Shin-ichi, Shinkawa, Hideichi, Weston, Mike D, Overbeck, Larry D, Hoover, Denise M, Kenyon, Judy B, Horai, Satoshi, Kimberling, William J

المصدر: European Journal of Human Genetics; Nov98, Vol. 6 Issue 6, p563, 7p

مصطلحات موضوعية: GENETICS of deafness, GENETIC disorders