Arama Sonuçları - Jan M. Friedman

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  1. 1
    Clinical and genetic aspects of neurofibromatosis 1

    Clinical and genetic aspects of neurofibromatosis 1 Yazar: Kimberly Jett, Jan M. Friedman

    Baskı/Yayın Bilgisi 2010
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  2. 2
    Neonatal alloimmune thrombocytopenic purpura and congenital porencephaly in two siblings associated with a "new" maternal antiplatelet antibody

    Neonatal alloimmune thrombocytopenic purpura and congenital porencephaly in two siblings associated with a "new" maternal antiplatelet antibody Yazar: Jan M. Friedman, RH Aster

    Baskı/Yayın Bilgisi 1985
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  3. 3
    MicroRNAs: critical mediators of differentiation, development and disease

    MicroRNAs: critical mediators of differentiation, development and disease Yazar: Jan M. Friedman, P. A. Jones

    Baskı/Yayın Bilgisi 2009
    Tam Metin Erişim
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  4. 4
    Teratogenic effects of drugs, a resource for clinicians (TERIS)

    Teratogenic effects of drugs, a resource for clinicians (TERIS) Yazar: Jan M. Friedman, Janine E. Polifka

    Baskı/Yayın Bilgisi 1994
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  5. 5
    Teratogen update: Azathioprine and 6‐mercaptopurine

    Teratogen update: Azathioprine and 6‐mercaptopurine Yazar: Janine E. Polifka, Jan M. Friedman

    Baskı/Yayın Bilgisi 2002
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  6. 6
    NF1 Gene and Neurofibromatosis 1

    NF1 Gene and Neurofibromatosis 1 Yazar: Sonja A. Rasmussen, Jan M. Friedman

    Baskı/Yayın Bilgisi 2000
    Tam Metin Erişim
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  7. 7
    Angiotensin II receptor antagonist treatment during pregnancy

    Angiotensin II receptor antagonist treatment during pregnancy Yazar: S Alwan, Janine E. Polifka, Jan M. Friedman

    Baskı/Yayın Bilgisi 2005
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  8. 8
    Mortality in Neurofibromatosis 1: An Analysis Using U.S. Death Certificates

    Mortality in Neurofibromatosis 1: An Analysis Using U.S. Death Certificates Yazar: Sonja A. Rasmussen, Quanhe Yang, Jan M. Friedman

    Baskı/Yayın Bilgisi 2001
    Tam Metin Erişim Tam Metin Erişim
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  9. 9
    Massively Parallel Sequencing: The Next Big Thing in Genetic Medicine

    Massively Parallel Sequencing: The Next Big Thing in Genetic Medicine Yazar: Tracy Tucker, Marco A. Marra, Jan M. Friedman

    Baskı/Yayın Bilgisi 2009
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  10. 10
    Value for Money? Array Genomic Hybridization for Diagnostic Testing for Genetic Causes of Intellectual Disability

    Value for Money? Array Genomic Hybridization for Diagnostic Testing for Genetic Causes of Intellectual Disability Yazar: Dean A. Regier, Jan M. Friedman, Carlo A. Marra

    Baskı/Yayın Bilgisi 2010
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  11. 11
    Incidental Findings from Clinical Genome‐Wide Sequencing: A Review

    Incidental Findings from Clinical Genome‐Wide Sequencing: A Review Yazar: Zoe Lohn, Shelin Adam, Patricia Birch, Jan M. Friedman

    Baskı/Yayın Bilgisi 2013
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  12. 12
    Paternalism and the ACMG recommendations on genomic incidental findings: patients seen but not heard

    Paternalism and the ACMG recommendations on genomic incidental findings: patients seen but not heard Yazar: Anne Townsend, Shelin Adam, Patricia Birch, Jan M. Friedman

    Baskı/Yayın Bilgisi 2013
    Tam Metin Erişim Tam Metin Erişim
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  13. 13
    Prevalence of Neurofibromatosis 1 in German Children at Elementary School Enrollment

    Prevalence of Neurofibromatosis 1 in German Children at Elementary School Enrollment Yazar: Marga Lammert, Jan M. Friedman, Lan Kluwe, Victor F. Mautner

    Baskı/Yayın Bilgisi 2005
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  14. 14
    Cellular promoters incorporated into the adenovirus genome: cell specificity of albumin and immunoglobulin expression.

    Cellular promoters incorporated into the adenovirus genome: cell specificity of albumin and immunoglobulin expression. Yazar: Jan M. Friedman, L E Babiss, David F. Clayton, James Darnell

    Baskı/Yayın Bilgisi 1986
    Tam Metin Erişim
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  15. 15
    Low risk of solid tumors in persons with Down syndrome

    Low risk of solid tumors in persons with Down syndrome Yazar: Henrik Hasle, Jan M. Friedman, Jørgen H. Olsen, Sonja A. Rasmussen

    Baskı/Yayın Bilgisi 2016
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  16. 16
    Straglr: discovering and genotyping tandem repeat expansions using whole genome long-read sequences

    Straglr: discovering and genotyping tandem repeat expansions using whole genome long-read sequences Yazar: Readman Chiu, Indhu‐Shree Rajan‐Babu, Jan M. Friedman, İnanç Birol

    Baskı/Yayın Bilgisi 2021
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  17. 17
    Specific SSRIs and birth defects: bayesian analysis to interpret new data in the context of previous reports

    Specific SSRIs and birth defects: bayesian analysis to interpret new data in the context of previous reports Yazar: Jennita Reefhuis, Owen Devine, Jan M. Friedman, Carol Louik, Margaret A. Honein

    Baskı/Yayın Bilgisi 2015
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  18. 18
    Use of Selective Serotonin-Reuptake Inhibitors in Pregnancy and the Risk of Birth Defects

    Use of Selective Serotonin-Reuptake Inhibitors in Pregnancy and the Risk of Birth Defects Yazar: Sura Alwan, Jennita Reefhuis, Sonja A. Rasmussen, Richard S. Olney, Jan M. Friedman

    Baskı/Yayın Bilgisi 2007
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  19. 19
    How many genes underlie the occurrence of common complex diseases in the population?

    How many genes underlie the occurrence of common complex diseases in the population? Yazar: Quanhe Yang, Muin J. Khoury, Jan M. Friedman, Julian Little, W. Dana Flanders

    Baskı/Yayın Bilgisi 2005
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  20. 20
    Improving the Prediction of Complex Diseases by Testing for Multiple Disease-Susceptibility Genes

    Improving the Prediction of Complex Diseases by Testing for Multiple Disease-Susceptibility Genes Yazar: Quanhe Yang, Muin J. Khoury, Lorenzo D. Botto, Jan M. Friedman, W. Dana Flanders

    Baskı/Yayın Bilgisi 2003
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