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H Peretz

Showing results (51-60 of 59) with videos related to

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Human Mutation|January 1, 1997
Cys 618 Arg mutation in the RET proto-oncogene associated with familial medullary thyroid carcinoma and maternally transmitted Hirschsprung's disease suggesting a role for imprintingH Peretz, R Luboshitsky, E Baron, et al.
American Journal of Medical Genetics. Part A|December 21, 2022
A de novo hexokinase 1 (HK1) variant presenting as Boucher-Neuhäuser syndromeRyan H Peretz, Wadih M Zein, Robert B Hufnagel, et al.
European Journal of Neurology|March 16, 2007
Triggered C-reactive protein (CRP) concentrations and the CRP gene -717A>G polymorphism in acute stroke or transient ischemic attackE Ben-Assayag, S Shenhar-Tsarfaty, I Bova, et al.
The Hematology Journal : the Official Journal of the European Haematology Association|March 29, 2002
Molecular characterization of four novel mutations causing factor VII deficiencyH Tamary, Y Fromovich-Amit, L Shalmon, et al.
Journal of Thrombosis and Haemostasis : JTH|December 20, 2005
A 13-bp deletion in alpha(IIb) gene is a founder mutation that predominates in Palestinian-Arab patients with Glanzmann thrombastheniaN Rosenberg, H Hauschner, H Peretz, et al.
Blood|November 5, 1997
The two common mutations causing factor XI deficiency in Jews stem from distinct founders: one of ancient Middle Eastern origin and another of more recent European originH Peretz, A Mulai, S Usher, et al.
European Journal of Human Genetics : EJHG|August 22, 2000
Two p16 (CDKN2A) germline mutations in 30 Israeli melanoma familiesE Yakobson, P Shemesh, E Azizi, et al.
Clinical Biochemistry|June 16, 2001
Cytokine network in nonresponding chronic hepatitis C patients with genotype 1: role of triple therapy with interferon alpha, ribavirin, and ursodeoxycholateM G Neuman, L M Blendis, N H Shear, et al.
The Journal of Clinical Endocrinology and Metabolism|December 22, 1999
Mendelian diseases among Roman Jews: implications for the origins of disease allelesC Oddoux, E Guillen-Navarro, C Ditivoli, et al.
Pageof 6

Showing results (51-60 of 59) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 59 results.
Human Mutation|January 1, 1997
Cys 618 Arg mutation in the RET proto-oncogene associated with familial medullary thyroid carcinoma and maternally transmitted Hirschsprung's disease suggesting a role for imprintingH Peretz, R Luboshitsky, E Baron, et al.
American Journal of Medical Genetics. Part A|December 21, 2022
A de novo hexokinase 1 (HK1) variant presenting as Boucher-Neuhäuser syndromeRyan H Peretz, Wadih M Zein, Robert B Hufnagel, et al.
European Journal of Neurology|March 16, 2007
Triggered C-reactive protein (CRP) concentrations and the CRP gene -717A>G polymorphism in acute stroke or transient ischemic attackE Ben-Assayag, S Shenhar-Tsarfaty, I Bova, et al.
The Hematology Journal : the Official Journal of the European Haematology Association|March 29, 2002
Molecular characterization of four novel mutations causing factor VII deficiencyH Tamary, Y Fromovich-Amit, L Shalmon, et al.
Journal of Thrombosis and Haemostasis : JTH|December 20, 2005
A 13-bp deletion in alpha(IIb) gene is a founder mutation that predominates in Palestinian-Arab patients with Glanzmann thrombastheniaN Rosenberg, H Hauschner, H Peretz, et al.
Blood|November 5, 1997
The two common mutations causing factor XI deficiency in Jews stem from distinct founders: one of ancient Middle Eastern origin and another of more recent European originH Peretz, A Mulai, S Usher, et al.
European Journal of Human Genetics : EJHG|August 22, 2000
Two p16 (CDKN2A) germline mutations in 30 Israeli melanoma familiesE Yakobson, P Shemesh, E Azizi, et al.
Clinical Biochemistry|June 16, 2001
Cytokine network in nonresponding chronic hepatitis C patients with genotype 1: role of triple therapy with interferon alpha, ribavirin, and ursodeoxycholateM G Neuman, L M Blendis, N H Shear, et al.
The Journal of Clinical Endocrinology and Metabolism|December 22, 1999
Mendelian diseases among Roman Jews: implications for the origins of disease allelesC Oddoux, E Guillen-Navarro, C Ditivoli, et al.
Pageof 6