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A Ravella

Showing results (11-20 of 19) with videos related to

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Journal of the American Academy of Dermatology|August 1, 1987
Localized pili canaliculi and trianguliA Ravella, R M Pujol, X Noguera, et al.
American Journal of Human Genetics|November 1, 1995
Molecular characterization of the breakpoints of a 12-kb deletion in the NF1 gene in a family showing germ-line mosaicismC Lázaro, A Gaona, M Lynch, et al.
Medicina Cutanea Ibero-Latino-Americana|January 1, 1988
[Multiple hamartoma syndrome]R M Pujol, A Ravella, X Noguera, et al.
Medicina Cutanea Ibero-Latino-Americana|January 1, 1987
[Ito's hypomelanosis]R M Pujol, A Ravella, A Alomar, et al.
Medicina Clinica|April 19, 1986
[Basal cell nevoid carcinoma syndrome]A Tuneu, J M Piera, A Ravella, et al.
Human Molecular Genetics|June 1, 1993
Novel alleles, hemizygosity and deletions at an Alu-repeat within the neurofibromatosis type 1 (NF1) geneC Lázaro, A Gaona, A Ravella, et al.
Human Genetics|June 21, 2001
Somatic NF1 mutational spectrum in benign neurofibromas: mRNA splice defects are common among point mutationsE Serra, E Ars, A Ravella, et al.
Journal of Medical Genetics|June 17, 2003
Recurrent mutations in the NF1 gene are common among neurofibromatosis type 1 patientsE Ars, H Kruyer, M Morell, et al.
The British Journal of Dermatology|February 1, 1994
Tufted hair folliculitis: a specific disease?R M Pujol, V García-Patos, A Ravella-Mateu, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Journal of the American Academy of Dermatology|August 1, 1987
Localized pili canaliculi and trianguliA Ravella, R M Pujol, X Noguera, et al.
American Journal of Human Genetics|November 1, 1995
Molecular characterization of the breakpoints of a 12-kb deletion in the NF1 gene in a family showing germ-line mosaicismC Lázaro, A Gaona, M Lynch, et al.
Medicina Cutanea Ibero-Latino-Americana|January 1, 1988
[Multiple hamartoma syndrome]R M Pujol, A Ravella, X Noguera, et al.
Medicina Cutanea Ibero-Latino-Americana|January 1, 1987
[Ito's hypomelanosis]R M Pujol, A Ravella, A Alomar, et al.
Medicina Clinica|April 19, 1986
[Basal cell nevoid carcinoma syndrome]A Tuneu, J M Piera, A Ravella, et al.
Human Molecular Genetics|June 1, 1993
Novel alleles, hemizygosity and deletions at an Alu-repeat within the neurofibromatosis type 1 (NF1) geneC Lázaro, A Gaona, A Ravella, et al.
Human Genetics|June 21, 2001
Somatic NF1 mutational spectrum in benign neurofibromas: mRNA splice defects are common among point mutationsE Serra, E Ars, A Ravella, et al.
Journal of Medical Genetics|June 17, 2003
Recurrent mutations in the NF1 gene are common among neurofibromatosis type 1 patientsE Ars, H Kruyer, M Morell, et al.
The British Journal of Dermatology|February 1, 1994
Tufted hair folliculitis: a specific disease?R M Pujol, V García-Patos, A Ravella-Mateu, et al.
Pageof 2