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A Bar-Shira

Showing results (11-20 of 28) with videos related to

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Neurology|October 17, 2007
The LRRK2 G2019S mutation in Ashkenazi Jews with Parkinson disease: is there a gender effect?A Orr-Urtreger, C Shifrin, U Rozovski, et al.
Journal of Neurology|August 3, 2015
The Alzheimer disease BIN1 locus as a modifier of GBA-associated Parkinson diseaseZ Gan-Or, I Amshalom, A Bar-Shira, et al.
American Journal of Human Genetics|April 29, 1998
Genotype-phenotype relationships in ataxia-telangiectasia and variantsS Gilad, L Chessa, R Khosravi, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|December 26, 2018
Microarray analysis has no additional value in fetal aberrant right subclavian artery: description of 268 pregnancies and systematic literature reviewL Sagi-Dain, A Singer, S Josefsberg, et al.
Journal of Neurology|August 25, 1999
Absence of mutations in ATM, the gene responsible for ataxia telangiectasia in patients with cerebellar ataxiaS Hassin-Baer, A Bar-Shira, S Gilad, et al.
Human Molecular Genetics|July 1, 1993
Paired STSs amplified from radiation hybrids, and from associated YACs, identify highly polymorphic loci flanking the ataxia telangiectasia locus on chromosome 11q22-23C M McConville, P J Byrd, H J Ambrose, et al.
Human Mutation|February 5, 1998
Identification of ATM mutations using extended RT-PCR and restriction endonuclease fingerprinting, and elucidation of the repertoire of A-T mutations in IsraelS Gilad, R Khosravi, R Harnik, et al.
Somatic Cell and Molecular Genetics|March 1, 1995
Human cDNA clones that modify radiomimetic sensitivity of ataxia-telangiectasia (group A) cellsY Ziv, A Bar-Shira, T J Jorgensen, et al.
Human Molecular Genetics|December 1, 1996
Ataxia-telangiectasia: founder effect among north African JewsS Gilad, A Bar-Shira, R Harnik, et al.
Human Genetics|April 1, 1995
A high-density microsatellite map of the ataxia-telangiectasia locusL Vanagaite, M R James, G Rotman, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
Neurology|October 17, 2007
The LRRK2 G2019S mutation in Ashkenazi Jews with Parkinson disease: is there a gender effect?A Orr-Urtreger, C Shifrin, U Rozovski, et al.
Journal of Neurology|August 3, 2015
The Alzheimer disease BIN1 locus as a modifier of GBA-associated Parkinson diseaseZ Gan-Or, I Amshalom, A Bar-Shira, et al.
American Journal of Human Genetics|April 29, 1998
Genotype-phenotype relationships in ataxia-telangiectasia and variantsS Gilad, L Chessa, R Khosravi, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|December 26, 2018
Microarray analysis has no additional value in fetal aberrant right subclavian artery: description of 268 pregnancies and systematic literature reviewL Sagi-Dain, A Singer, S Josefsberg, et al.
Journal of Neurology|August 25, 1999
Absence of mutations in ATM, the gene responsible for ataxia telangiectasia in patients with cerebellar ataxiaS Hassin-Baer, A Bar-Shira, S Gilad, et al.
Human Molecular Genetics|July 1, 1993
Paired STSs amplified from radiation hybrids, and from associated YACs, identify highly polymorphic loci flanking the ataxia telangiectasia locus on chromosome 11q22-23C M McConville, P J Byrd, H J Ambrose, et al.
Human Mutation|February 5, 1998
Identification of ATM mutations using extended RT-PCR and restriction endonuclease fingerprinting, and elucidation of the repertoire of A-T mutations in IsraelS Gilad, R Khosravi, R Harnik, et al.
Somatic Cell and Molecular Genetics|March 1, 1995
Human cDNA clones that modify radiomimetic sensitivity of ataxia-telangiectasia (group A) cellsY Ziv, A Bar-Shira, T J Jorgensen, et al.
Human Molecular Genetics|December 1, 1996
Ataxia-telangiectasia: founder effect among north African JewsS Gilad, A Bar-Shira, R Harnik, et al.
Human Genetics|April 1, 1995
A high-density microsatellite map of the ataxia-telangiectasia locusL Vanagaite, M R James, G Rotman, et al.
Pageof 3