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S MacKay

Showing results (271-280 of 312) with videos related to

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Studies in Health Technology and Informatics|April 25, 2001
Web-based surgical educational toolsN W John, M Riding, N I Phillips, et al.
Thorax|September 1, 1986
Short duration combination chemotherapy in the treatment of small cell lung cancerA J Dorward, S W Banham, A W Hutcheon, et al.
The American Review of Respiratory Disease|July 1, 1992
Immunohistology of the nasal mucosa following allergen-induced rhinitis. Identification of activated T lymphocytes, eosinophils, and neutrophilsV A Varney, M R Jacobson, R M Sudderick, et al.
American Journal of Human Genetics|November 3, 2009
Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humansZheng Li, Panagiotis I Sergouniotis, Michel Michaelides, et al.
Molecular Vision|January 21, 2010
Biallelic mutation of protocadherin-21 (PCDH21) causes retinal degeneration in humansRobert H Henderson, Zheng Li, Mai M Abd El Aziz, et al.
Transactions of the Royal Society of Tropical Medicine and Hygiene|July 1, 1994
An urban outbreak of visceral leishmaniasis in Natal, BrazilS M Jeronimo, R M Oliveira, S Mackay, et al.
Investigative Ophthalmology & Visual Science|February 12, 2011
Screening of SPATA7 in patients with Leber congenital amaurosis and severe childhood-onset retinal dystrophy reveals disease-causing mutationsDonna S Mackay, Louise A Ocaka, Arundhati Dev Borman, et al.
Molecular Vision|April 3, 2010
A detailed phenotypic assessment of individuals affected by MFRP-related oculopathyRajarshi Mukhopadhyay, Panagiotis I Sergouniotis, Donna S Mackay, et al.
Ophthalmology|June 18, 2013
The clinical effect of homozygous ABCA4 alleles in 18 patientsKaoru Fujinami, Panagiotis I Sergouniotis, Alice E Davidson, et al.
Human Molecular Genetics|July 28, 2007
SNP genome scanning localizes oto-dental syndrome to chromosome 11q13 and microdeletions at this locus implicate FGF3 in dental and inner-ear disease and FADD in ocular colobomaCheryl Y Gregory-Evans, Mariya Moosajee, Matthew D Hodges, et al.
Pageof 32

Showing results (271-280 of 312) with videos related to

Sort By:
Pageof 32
Studies in Health Technology and Informatics|April 25, 2001
Web-based surgical educational toolsN W John, M Riding, N I Phillips, et al.
Thorax|September 1, 1986
Short duration combination chemotherapy in the treatment of small cell lung cancerA J Dorward, S W Banham, A W Hutcheon, et al.
The American Review of Respiratory Disease|July 1, 1992
Immunohistology of the nasal mucosa following allergen-induced rhinitis. Identification of activated T lymphocytes, eosinophils, and neutrophilsV A Varney, M R Jacobson, R M Sudderick, et al.
American Journal of Human Genetics|November 3, 2009
Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humansZheng Li, Panagiotis I Sergouniotis, Michel Michaelides, et al.
Molecular Vision|January 21, 2010
Biallelic mutation of protocadherin-21 (PCDH21) causes retinal degeneration in humansRobert H Henderson, Zheng Li, Mai M Abd El Aziz, et al.
Transactions of the Royal Society of Tropical Medicine and Hygiene|July 1, 1994
An urban outbreak of visceral leishmaniasis in Natal, BrazilS M Jeronimo, R M Oliveira, S Mackay, et al.
Investigative Ophthalmology & Visual Science|February 12, 2011
Screening of SPATA7 in patients with Leber congenital amaurosis and severe childhood-onset retinal dystrophy reveals disease-causing mutationsDonna S Mackay, Louise A Ocaka, Arundhati Dev Borman, et al.
Molecular Vision|April 3, 2010
A detailed phenotypic assessment of individuals affected by MFRP-related oculopathyRajarshi Mukhopadhyay, Panagiotis I Sergouniotis, Donna S Mackay, et al.
Ophthalmology|June 18, 2013
The clinical effect of homozygous ABCA4 alleles in 18 patientsKaoru Fujinami, Panagiotis I Sergouniotis, Alice E Davidson, et al.
Human Molecular Genetics|July 28, 2007
SNP genome scanning localizes oto-dental syndrome to chromosome 11q13 and microdeletions at this locus implicate FGF3 in dental and inner-ear disease and FADD in ocular colobomaCheryl Y Gregory-Evans, Mariya Moosajee, Matthew D Hodges, et al.
Pageof 32