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J Ignatius

Showing results (61-70 of 91) with videos related to

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American Journal of Human Genetics|March 11, 2000
Assignment of a novel locus for autosomal recessive congenital ichthyosis to chromosome 19p13.1-p13.2E Virolainen, M Wessman, I Hovatta, et al.
Human Mutation|June 30, 2000
A CRX mutation in a Finnish family with dominant cone-rod retinal dystrophyE M Sankila, T H Joensuu, R H Hämäläinen, et al.
Lancet (London, England)|July 29, 1995
SMN gene deletion in variant of infantile spinal muscular atrophyL Bürglen, R Spiegel, J Ignatius, et al.
Neuropediatrics|December 22, 1999
Clinical spectrum and diagnostic difficulties of infantile ponto-cerebellar hypoplasia type 1F Muntoni, F Goodwin, C Sewry, et al.
Journal of Medical Genetics|February 1, 1996
Gene deletions in spinal muscular atrophyN R Rodrigues, N Owen, K Talbot, et al.
American Journal of Preventive Medicine|September 1, 1986
Effects of labeling and treatment of hypertension on perceived healthL C Harlan, B F Polk, S Cooper, et al.
American Journal of Epidemiology|January 1, 1984
Disability days associated with detection and treatment in a hypertension control programB F Polk, L C Harlan, S P Cooper, et al.
Developmental Neuroscience|January 1, 1989
Integrins and cell adhesion molecules: neuronal receptors that regulate axon growth on extracellular matrices and cell surfacesL F Reichardt, J L Bixby, D E Hall, et al.
The British Journal of Dermatology|November 11, 2010
Multiple miliary osteoma cutis is a distinct disease entity: four case reports and review of the literatureR M Myllylä, K M Haapasaari, R Palatsi, et al.
American Journal of Human Genetics|July 31, 1998
Assignment of the disease locus for lethal congenital contracture syndrome to a restricted region of chromosome 9q34, by genome scan using five affected individualsP Mäkelä-Bengs, N Järvinen, K Vuopala, et al.
Pageof 10

Showing results (61-70 of 91) with videos related to

Sort By:
Pageof 10
American Journal of Human Genetics|March 11, 2000
Assignment of a novel locus for autosomal recessive congenital ichthyosis to chromosome 19p13.1-p13.2E Virolainen, M Wessman, I Hovatta, et al.
Human Mutation|June 30, 2000
A CRX mutation in a Finnish family with dominant cone-rod retinal dystrophyE M Sankila, T H Joensuu, R H Hämäläinen, et al.
Lancet (London, England)|July 29, 1995
SMN gene deletion in variant of infantile spinal muscular atrophyL Bürglen, R Spiegel, J Ignatius, et al.
Neuropediatrics|December 22, 1999
Clinical spectrum and diagnostic difficulties of infantile ponto-cerebellar hypoplasia type 1F Muntoni, F Goodwin, C Sewry, et al.
Journal of Medical Genetics|February 1, 1996
Gene deletions in spinal muscular atrophyN R Rodrigues, N Owen, K Talbot, et al.
American Journal of Preventive Medicine|September 1, 1986
Effects of labeling and treatment of hypertension on perceived healthL C Harlan, B F Polk, S Cooper, et al.
American Journal of Epidemiology|January 1, 1984
Disability days associated with detection and treatment in a hypertension control programB F Polk, L C Harlan, S P Cooper, et al.
Developmental Neuroscience|January 1, 1989
Integrins and cell adhesion molecules: neuronal receptors that regulate axon growth on extracellular matrices and cell surfacesL F Reichardt, J L Bixby, D E Hall, et al.
The British Journal of Dermatology|November 11, 2010
Multiple miliary osteoma cutis is a distinct disease entity: four case reports and review of the literatureR M Myllylä, K M Haapasaari, R Palatsi, et al.
American Journal of Human Genetics|July 31, 1998
Assignment of the disease locus for lethal congenital contracture syndrome to a restricted region of chromosome 9q34, by genome scan using five affected individualsP Mäkelä-Bengs, N Järvinen, K Vuopala, et al.
Pageof 10