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D Viskochil

Showing results (31-40 of 38) with videos related to

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Genomics|August 1, 1990
Identification and characterization of transcripts from the neurofibromatosis 1 region: the sequence and genomic structure of EVI2 and mapping of other transcriptsR M Cawthon, P O'Connell, A M Buchberg, et al.
Familial Cancer|July 26, 2012
Parent-of-origin in individuals with familial neurofibromatosis type 1 and optic pathway gliomasK J Johnson, M J Fisher, R L Listernick, et al.
Cell|July 13, 1990
Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locusD Viskochil, A M Buchberg, G Xu, et al.
Genomics|March 1, 1991
cDNA sequence and genomic structure of EV12B, a gene lying within an intron of the neurofibromatosis type 1 geneR M Cawthon, L B Andersen, A M Buchberg, et al.
American Journal of Medical Genetics. Part A|May 3, 2025
Worth the Effort: Lessons for Discovery and Care From an Unusual Case of Gorlin SyndromeV Taliercio, J Zhao, S E Boyden, et al.
The Journal of Pediatrics|December 1, 1996
Sudden death in Williams syndrome: report of ten casesL M Bird, G F Billman, R V Lacro, et al.
American Journal of Human Genetics|December 13, 2006
An absence of cutaneous neurofibromas associated with a 3-bp inframe deletion in exon 17 of the NF1 gene (c.2970-2972 delAAT): evidence of a clinically significant NF1 genotype-phenotype correlationM Upadhyaya, S M Huson, M Davies, et al.
American Journal of Medical Genetics. Part A|September 19, 2009
Expanding CEP290 mutational spectrum in ciliopathiesLorena Travaglini, Francesco Brancati, Tania Attie-Bitach, et al.
Pageof 4

Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
Genomics|August 1, 1990
Identification and characterization of transcripts from the neurofibromatosis 1 region: the sequence and genomic structure of EVI2 and mapping of other transcriptsR M Cawthon, P O'Connell, A M Buchberg, et al.
Familial Cancer|July 26, 2012
Parent-of-origin in individuals with familial neurofibromatosis type 1 and optic pathway gliomasK J Johnson, M J Fisher, R L Listernick, et al.
Cell|July 13, 1990
Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locusD Viskochil, A M Buchberg, G Xu, et al.
Genomics|March 1, 1991
cDNA sequence and genomic structure of EV12B, a gene lying within an intron of the neurofibromatosis type 1 geneR M Cawthon, L B Andersen, A M Buchberg, et al.
American Journal of Medical Genetics. Part A|May 3, 2025
Worth the Effort: Lessons for Discovery and Care From an Unusual Case of Gorlin SyndromeV Taliercio, J Zhao, S E Boyden, et al.
The Journal of Pediatrics|December 1, 1996
Sudden death in Williams syndrome: report of ten casesL M Bird, G F Billman, R V Lacro, et al.
American Journal of Human Genetics|December 13, 2006
An absence of cutaneous neurofibromas associated with a 3-bp inframe deletion in exon 17 of the NF1 gene (c.2970-2972 delAAT): evidence of a clinically significant NF1 genotype-phenotype correlationM Upadhyaya, S M Huson, M Davies, et al.
American Journal of Medical Genetics. Part A|September 19, 2009
Expanding CEP290 mutational spectrum in ciliopathiesLorena Travaglini, Francesco Brancati, Tania Attie-Bitach, et al.
Pageof 4