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Hane Lee

Showing results (31-40 of 134) with videos related to

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Human Molecular Genetics|December 7, 2005
A genome-wide linkage scan of familial benign recurrent vertigo: linkage to 22q12 with evidence of heterogeneityHane Lee, Joanna C Jen, Hui Wang, et al.
BMC Genomics|January 2, 2010
Improving the efficiency of genomic loci capture using oligonucleotide arrays for high throughput resequencingHane Lee, Brian D O'Connor, Barry Merriman, et al.
Cornea|February 18, 2025
Corneal Myofibromatous and Pterygium-Like Changes in a Family With a PDGFRB VariantIrving M Raber, Ashley Khalili, Rin Khang, et al.
Journal of Medical Genetics|March 29, 2014
Expanding the phenotype of mutations in DICER1: mosaic missense mutations in the RNase IIIb domain of DICER1 cause GLOW syndromeSteven Klein, Hane Lee, Shahnaz Ghahremani, et al.
Annals of Human Genetics|November 15, 2024
Secondary findings in 443 exome sequencing dataMarija Branković, Heonjong Han, Milena Janković, et al.
Bioinformatics (Oxford, England)|August 11, 2011
Exome sequencing-based copy-number variation and loss of heterozygosity detection: ExomeCNVJarupon Fah Sathirapongsasuti, Hane Lee, Basil A J Horst, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 17, 2010
Accuracy of phenotyping of autistic children based on Internet implemented parent reportHane Lee, Alison R Marvin, Tamara Watson, et al.
Retina (Philadelphia, Pa.)|June 20, 2023
LONG-TERM CLINICAL OUTCOMES AND GENOTYPE-PHENOTYPE CORRELATION IN FAMILIAL EXUDATIVE VITREORETINOPATHY IN A TERTIARY REFERRAL CENTERAndrew S H Tsai, Eugene Y C Kang, Nan-Kai Wang, et al.
Molecular Genetics & Genomic Medicine|January 21, 2025
A Korean Patient With Leber Congenital Amaurosis and a Homozygous RPE65 Variant Originating From a Paternal Uniparental IsodisomyHane Lee, Dongseok Moon, Rin Khang, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|February 11, 2020
Myopathy associated with homozygous PYROXD1 pathogenic variants detected by genome sequencingJeremy D Woods, Negar Khanlou, Hane Lee, et al.
Pageof 14

Showing results (31-40 of 134) with videos related to

Sort By:
Pageof 14
Human Molecular Genetics|December 7, 2005
A genome-wide linkage scan of familial benign recurrent vertigo: linkage to 22q12 with evidence of heterogeneityHane Lee, Joanna C Jen, Hui Wang, et al.
BMC Genomics|January 2, 2010
Improving the efficiency of genomic loci capture using oligonucleotide arrays for high throughput resequencingHane Lee, Brian D O'Connor, Barry Merriman, et al.
Cornea|February 18, 2025
Corneal Myofibromatous and Pterygium-Like Changes in a Family With a PDGFRB VariantIrving M Raber, Ashley Khalili, Rin Khang, et al.
Journal of Medical Genetics|March 29, 2014
Expanding the phenotype of mutations in DICER1: mosaic missense mutations in the RNase IIIb domain of DICER1 cause GLOW syndromeSteven Klein, Hane Lee, Shahnaz Ghahremani, et al.
Annals of Human Genetics|November 15, 2024
Secondary findings in 443 exome sequencing dataMarija Branković, Heonjong Han, Milena Janković, et al.
Bioinformatics (Oxford, England)|August 11, 2011
Exome sequencing-based copy-number variation and loss of heterozygosity detection: ExomeCNVJarupon Fah Sathirapongsasuti, Hane Lee, Basil A J Horst, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 17, 2010
Accuracy of phenotyping of autistic children based on Internet implemented parent reportHane Lee, Alison R Marvin, Tamara Watson, et al.
Retina (Philadelphia, Pa.)|June 20, 2023
LONG-TERM CLINICAL OUTCOMES AND GENOTYPE-PHENOTYPE CORRELATION IN FAMILIAL EXUDATIVE VITREORETINOPATHY IN A TERTIARY REFERRAL CENTERAndrew S H Tsai, Eugene Y C Kang, Nan-Kai Wang, et al.
Molecular Genetics & Genomic Medicine|January 21, 2025
A Korean Patient With Leber Congenital Amaurosis and a Homozygous RPE65 Variant Originating From a Paternal Uniparental IsodisomyHane Lee, Dongseok Moon, Rin Khang, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|February 11, 2020
Myopathy associated with homozygous PYROXD1 pathogenic variants detected by genome sequencingJeremy D Woods, Negar Khanlou, Hane Lee, et al.
Pageof 14