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Showing results (51-60 of 57) with videos related to

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Human Genetics|February 24, 2001
Diverse prevalence of large deletions within the OA1 gene in ocular albinism type 1 patients from Europe and North AmericaM T Bassi, A A Bergen, P Bitoun, et al.
Genes, Chromosomes & Cancer|August 26, 1998
Molecular analysis of 1p36 breakpoints in two Merkel cell carcinomasM Van Gele, N Van Roy, S G Ronan, et al.
Journal of Medical Genetics|June 10, 2005
Identification of novel deletion breakpoints bordered by segmental duplications in the NF1 locus using high resolution array-CGHK K Mantripragada, A-C Thuresson, A Piotrowski, et al.
Science (New York, N.Y.)|November 17, 2018
Mutations in LZTR1 drive human disease by dysregulating RAS ubiquitinationM Steklov, S Pandolfi, M F Baietti, 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.
Cytogenetics and Cell Genetics|January 1, 1996
Report of the sixth international workshop on human chromosome 3 mapping 1995S L Naylor, B Carritt, C Boileau, et al.
Human Molecular Genetics|July 27, 2001
Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype--phenotype correlationE De Baere, M J Dixon, K W Small, et al.
Pageof 6

Showing results (51-60 of 57) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 57 results.
Human Genetics|February 24, 2001
Diverse prevalence of large deletions within the OA1 gene in ocular albinism type 1 patients from Europe and North AmericaM T Bassi, A A Bergen, P Bitoun, et al.
Genes, Chromosomes & Cancer|August 26, 1998
Molecular analysis of 1p36 breakpoints in two Merkel cell carcinomasM Van Gele, N Van Roy, S G Ronan, et al.
Journal of Medical Genetics|June 10, 2005
Identification of novel deletion breakpoints bordered by segmental duplications in the NF1 locus using high resolution array-CGHK K Mantripragada, A-C Thuresson, A Piotrowski, et al.
Science (New York, N.Y.)|November 17, 2018
Mutations in LZTR1 drive human disease by dysregulating RAS ubiquitinationM Steklov, S Pandolfi, M F Baietti, 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.
Cytogenetics and Cell Genetics|January 1, 1996
Report of the sixth international workshop on human chromosome 3 mapping 1995S L Naylor, B Carritt, C Boileau, et al.
Human Molecular Genetics|July 27, 2001
Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype--phenotype correlationE De Baere, M J Dixon, K W Small, et al.
Pageof 6