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W L Alward

Showing results (51-60 of 73) with videos related to

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American Journal of Ophthalmology|January 23, 1998
Autosomal dominant iris hypoplasia is caused by a mutation in the Rieger syndrome (RIEG/PITX2) geneW L Alward, E V Semina, J W Kalenak, et al.
Genome Research|September 1, 1996
Fine mapping of the autosomal dominant juvenile open angle glaucoma (GLC1A) region and evaluation of candidate genesS L Sunden, W L Alward, B E Nichols, et al.
Nature Genetics|May 1, 1993
Genetic linkage of familial open angle glaucoma to chromosome 1q21-q31V C Sheffield, E M Stone, W L Alward, et al.
Investigative Ophthalmology & Visual Science|September 28, 2000
Localization of MYOC transcripts in human eye and optic nerve by in situ hybridizationR E Swiderski, J L Ross, J H Fingert, et al.
The Journal of Infectious Diseases|April 1, 1985
Acute hepatitis B virus infection: relation of age to the clinical expression of disease and subsequent development of the carrier stateB J McMahon, W L Alward, D B Hall, et al.
Genome Research|June 13, 1998
Characterization and comparison of the human and mouse GLC1A glaucoma genesJ H Fingert, L Ying, R E Swiderski, et al.
Journal of Glaucoma|December 12, 2001
Screening for mutations of Axenfeld-Rieger syndrome caused by FOXC1 gene in Japanese patientsC Kawase, K Kawase, T Taniguchi, et al.
Nature Genetics|June 10, 1998
A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMDE V Semina, R E Ferrell, H A Mintz-Hittner, et al.
Human Molecular Genetics|August 1, 1995
Linkage of autosomal dominant iris hypoplasia to the region of the Rieger syndrome locus (4q25)E Héon, B P Sheth, J W Kalenak, et al.
Nature Genetics|September 1, 1992
Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4J C Murray, S R Bennett, A E Kwitek, et al.
Pageof 8

Showing results (51-60 of 73) with videos related to

Sort By:
Pageof 8
American Journal of Ophthalmology|January 23, 1998
Autosomal dominant iris hypoplasia is caused by a mutation in the Rieger syndrome (RIEG/PITX2) geneW L Alward, E V Semina, J W Kalenak, et al.
Genome Research|September 1, 1996
Fine mapping of the autosomal dominant juvenile open angle glaucoma (GLC1A) region and evaluation of candidate genesS L Sunden, W L Alward, B E Nichols, et al.
Nature Genetics|May 1, 1993
Genetic linkage of familial open angle glaucoma to chromosome 1q21-q31V C Sheffield, E M Stone, W L Alward, et al.
Investigative Ophthalmology & Visual Science|September 28, 2000
Localization of MYOC transcripts in human eye and optic nerve by in situ hybridizationR E Swiderski, J L Ross, J H Fingert, et al.
The Journal of Infectious Diseases|April 1, 1985
Acute hepatitis B virus infection: relation of age to the clinical expression of disease and subsequent development of the carrier stateB J McMahon, W L Alward, D B Hall, et al.
Genome Research|June 13, 1998
Characterization and comparison of the human and mouse GLC1A glaucoma genesJ H Fingert, L Ying, R E Swiderski, et al.
Journal of Glaucoma|December 12, 2001
Screening for mutations of Axenfeld-Rieger syndrome caused by FOXC1 gene in Japanese patientsC Kawase, K Kawase, T Taniguchi, et al.
Nature Genetics|June 10, 1998
A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMDE V Semina, R E Ferrell, H A Mintz-Hittner, et al.
Human Molecular Genetics|August 1, 1995
Linkage of autosomal dominant iris hypoplasia to the region of the Rieger syndrome locus (4q25)E Héon, B P Sheth, J W Kalenak, et al.
Nature Genetics|September 1, 1992
Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4J C Murray, S R Bennett, A E Kwitek, et al.
Pageof 8