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D Stambolian

Showing results (21-30 of 29) with videos related to

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Genome Research|October 1, 1996
Fine structure of the human galactokinase GALK1 geneD J Bergsma, Y Ai, W R Skach, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 1, 1997
Genetic mapping of a mouse ocular malformation locus, Tcm, to chromosome 4E Zhou, P Grimes, J Favor, et al.
Genomics|July 20, 1995
Mapping of the 75-kDa inositol polyphosphate-5-phosphatase (Inpp5b) to distal mouse chromosome 4 and its exclusion as a candidate gene for dysgenetic lensP A Jänne, J M Rochelle, P A Martin-DeLeon, et al.
Eye (London, England)|November 8, 2014
Drusen and RPE atrophy automated quantification by optical coherence tomography in an elderly populationB Diniz, D C Rodger, V R Chavali, et al.
Human Heredity|November 20, 2001
A novel approach to search for identity by descent in small samples of patients and controls from the same mendelian breeding unit: a pilot study on myopiaS Heath, R Robledo, W Beggs, et al.
Human Molecular Genetics|August 1, 2000
A mouse model of galactose-induced cataractsY Ai, Z Zheng, A O'Brien-Jenkins, et al.
Human Molecular Genetics|April 3, 2010
Transcriptome analysis and molecular signature of human retinal pigment epitheliumN V Strunnikova, A Maminishkis, J J Barb, et al.
Human Mutation|May 2, 2000
Novel mutations in 13 probands with galactokinase deficiencyV Kolosha, E Anoia, C de Cespedes, et al.
American Journal of Human Genetics|May 29, 2000
Additional copies of the proteolipid protein gene causing Pelizaeus-Merzbacher disease arise by separate integration into the X chromosomeM E Hodes, K Woodward, N B Spinner, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Genome Research|October 1, 1996
Fine structure of the human galactokinase GALK1 geneD J Bergsma, Y Ai, W R Skach, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 1, 1997
Genetic mapping of a mouse ocular malformation locus, Tcm, to chromosome 4E Zhou, P Grimes, J Favor, et al.
Genomics|July 20, 1995
Mapping of the 75-kDa inositol polyphosphate-5-phosphatase (Inpp5b) to distal mouse chromosome 4 and its exclusion as a candidate gene for dysgenetic lensP A Jänne, J M Rochelle, P A Martin-DeLeon, et al.
Eye (London, England)|November 8, 2014
Drusen and RPE atrophy automated quantification by optical coherence tomography in an elderly populationB Diniz, D C Rodger, V R Chavali, et al.
Human Heredity|November 20, 2001
A novel approach to search for identity by descent in small samples of patients and controls from the same mendelian breeding unit: a pilot study on myopiaS Heath, R Robledo, W Beggs, et al.
Human Molecular Genetics|August 1, 2000
A mouse model of galactose-induced cataractsY Ai, Z Zheng, A O'Brien-Jenkins, et al.
Human Molecular Genetics|April 3, 2010
Transcriptome analysis and molecular signature of human retinal pigment epitheliumN V Strunnikova, A Maminishkis, J J Barb, et al.
Human Mutation|May 2, 2000
Novel mutations in 13 probands with galactokinase deficiencyV Kolosha, E Anoia, C de Cespedes, et al.
American Journal of Human Genetics|May 29, 2000
Additional copies of the proteolipid protein gene causing Pelizaeus-Merzbacher disease arise by separate integration into the X chromosomeM E Hodes, K Woodward, N B Spinner, et al.
Pageof 3