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H Peretz

Showing results (41-50 of 59) with videos related to

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Blood|August 8, 1998
A single genetic origin for the common prothrombotic G20210A polymorphism in the prothrombin geneA Zivelin, N Rosenberg, S Faier, et al.
Pediatric Neurology|April 10, 2026
Neurodevelopmental Symptoms Associated With MIRAGE Syndrome: A Case Report of Three Children and Review of the LiteratureEmily Garavatti, Ryan H Peretz, Cristian Cruz, et al.
Blood|January 15, 1995
One of the two common mutations causing factor XI deficiency in Ashkenazi Jews (type II) is also prevalent in Iraqi Jews, who represent the ancient gene pool of JewsO Shpilberg, H Peretz, A Zivelin, et al.
Journal of Thrombosis and Haemostasis : JTH|August 2, 2006
Diversity of Glanzmann thrombasthenia in southern India: 10 novel mutations identified among 15 unrelated patientsE J R Nelson, S C Nair, H Peretz, et al.
Clinical Chemistry and Laboratory Medicine|November 7, 1998
Screening for tumour suppressor p16(CDKN2A) germline mutations in Israeli melanoma familiesE A Yakobson, A Zlotogorski, R Shafir, et al.
Journal of Thrombosis and Haemostasis : JTH|May 14, 2004
A common ancestral mutation (C128X) occurring in 11 non-Jewish families from the UK with factor XI deficiencyP H B Bolton-Maggs, H Peretz, R Butler, et al.
Journal of Medical Genetics|May 3, 2005
Search for genetic variants associated with cutaneous malignant melanoma in the Ashkenazi Jewish populationJ C Y Loo, A D Paterson, A Hao, et al.
Mediators of Inflammation|January 1, 1994
Differential Proliferative Characteristics of Alveolar Fibroblasts in Interstitial Lung Diseases: Regulative Role of IL-1 and PGE(2)E Fireman, S Ben Efraim, J Greif, et al.
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.
Genetic Testing|January 6, 2001
The risk of fragile X premutation expansion is lower in carriers detected by general prenatal screening than in carriers from known fragile X familiesE Geva, Y Yaron, R Shomrat, et al.
Pageof 6

Showing results (41-50 of 59) with videos related to

Sort By:
Pageof 6
Blood|August 8, 1998
A single genetic origin for the common prothrombotic G20210A polymorphism in the prothrombin geneA Zivelin, N Rosenberg, S Faier, et al.
Pediatric Neurology|April 10, 2026
Neurodevelopmental Symptoms Associated With MIRAGE Syndrome: A Case Report of Three Children and Review of the LiteratureEmily Garavatti, Ryan H Peretz, Cristian Cruz, et al.
Blood|January 15, 1995
One of the two common mutations causing factor XI deficiency in Ashkenazi Jews (type II) is also prevalent in Iraqi Jews, who represent the ancient gene pool of JewsO Shpilberg, H Peretz, A Zivelin, et al.
Journal of Thrombosis and Haemostasis : JTH|August 2, 2006
Diversity of Glanzmann thrombasthenia in southern India: 10 novel mutations identified among 15 unrelated patientsE J R Nelson, S C Nair, H Peretz, et al.
Clinical Chemistry and Laboratory Medicine|November 7, 1998
Screening for tumour suppressor p16(CDKN2A) germline mutations in Israeli melanoma familiesE A Yakobson, A Zlotogorski, R Shafir, et al.
Journal of Thrombosis and Haemostasis : JTH|May 14, 2004
A common ancestral mutation (C128X) occurring in 11 non-Jewish families from the UK with factor XI deficiencyP H B Bolton-Maggs, H Peretz, R Butler, et al.
Journal of Medical Genetics|May 3, 2005
Search for genetic variants associated with cutaneous malignant melanoma in the Ashkenazi Jewish populationJ C Y Loo, A D Paterson, A Hao, et al.
Mediators of Inflammation|January 1, 1994
Differential Proliferative Characteristics of Alveolar Fibroblasts in Interstitial Lung Diseases: Regulative Role of IL-1 and PGE(2)E Fireman, S Ben Efraim, J Greif, et al.
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.
Genetic Testing|January 6, 2001
The risk of fragile X premutation expansion is lower in carriers detected by general prenatal screening than in carriers from known fragile X familiesE Geva, Y Yaron, R Shomrat, et al.
Pageof 6