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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 imprinting
H 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 syndrome
Ryan 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 attack
E 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 deficiency
H 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 thrombasthenia
N 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 origin
H 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 families
E 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 ursodeoxycholate
M 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 alleles
C Oddoux, E Guillen-Navarro, C Ditivoli, et al.
Page
of 6
Search research articles
Search
Showing results (51-60 of 59) with videos related to
Sort By:
Page
of 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 imprinting
H 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 syndrome
Ryan 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 attack
E 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 deficiency
H 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 thrombasthenia
N 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 origin
H 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 families
E 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 ursodeoxycholate
M 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 alleles
C Oddoux, E Guillen-Navarro, C Ditivoli, et al.
Page
of 6