Search Results - Nancy B. Spinner

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  1. 1
    Alagille Syndrome: Genetics and Functional Models

    Alagille Syndrome: Genetics and Functional Models by Melissa A. Gilbert, Nancy B. Spinner

    Published 2017
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  2. 2
    Notch signaling in human development and disease

    Notch signaling in human development and disease by Andrea Penton, Laura D. Leonard, Nancy B. Spinner

    Published 2012
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  3. 3
    Jagged1 (JAG1): Structure, expression, and disease associations

    Jagged1 (JAG1): Structure, expression, and disease associations by Christopher M. Grochowski, Kathleen M. Loomes, Nancy B. Spinner

    Published 2015
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  4. 4
    Alagille syndrome.

    Alagille syndrome. by Ian D. Krantz, David A. Piccoli, Nancy B. Spinner

    Published 1997
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  5. 5
    Unique forms of human and mouse nuclear receptor corepressor SMRT

    Unique forms of human and mouse nuclear receptor corepressor SMRT by Peter Ordentlich, Michael Downes, Wen Xie, Anna Genin, Nancy B. Spinner, Ronald M. Evans

    Published 1999
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  6. 6
    Genomic Diagnosis for Pediatric Disorders: Revolution and Evolution

    Genomic Diagnosis for Pediatric Disorders: Revolution and Evolution by Emilie Lalonde, Stefan Rentas, Fumin Lin, Matthew C. Dulik, Cara Skraban, Nancy B. Spinner

    Published 2020
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  7. 7
    Prenatal DNA Sequencing: Clinical, Counseling, and Diagnostic Laboratory Considerations

    Prenatal DNA Sequencing: Clinical, Counseling, and Diagnostic Laboratory Considerations by Ahmad Abou Tayoun, Nancy B. Spinner, Heidi L. Rehm, Robert C. Green, Diana W. Bianchi

    Published 2017
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  8. 8
    Parents’ Perceptions of the Usefulness of Chromosomal Microarray Analysis for Children with Autism Spectrum Disorders

    Parents’ Perceptions of the Usefulness of Chromosomal Microarray Analysis for Children with Autism Spectrum Disorders by Marian Reiff, Ellen Giarelli, Barbara A. Bernhardt, Ebony Easley, Nancy B. Spinner, Pamela Sankar, Surabhi Mulchandani

    Published 2015
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  9. 9
    The human osmoregulatory Na+/myo-inositol cotransporter gene (SLC5A3): molecular cloning and localization to chromosome 21

    The human osmoregulatory Na+/myo-inositol cotransporter gene (SLC5A3): molecular cloning and localization to chromosome 21 by Gerard T. Berry, John Mallee, H. Moo Kwon, Jong S. Rim, Wadia R. Mulla, Maximilian Muenke, Nancy B. Spinner

    Published 1995
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  10. 10
    Effect of Kasai Procedure on Hepatic Outcome in Alagille Syndrome

    Effect of Kasai Procedure on Hepatic Outcome in Alagille Syndrome by Adam J. Kaye, Elizabeth B. Rand, Pedro S Munoz, Nancy B. Spinner, Alan W. Flake, Binita M. Kamath

    Published 2010
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  11. 11
    “What does it mean?”: Uncertainties in understanding results of chromosomal microarray testing

    “What does it mean?”: Uncertainties in understanding results of chromosomal microarray testing by Marian Reiff, Barbara A. Bernhardt, Surabhi Mulchandani, Danielle Soucier, Diana Cornell, Reed E. Pyeritz, Nancy B. Spinner

    Published 2012
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  12. 12
    Features of Alagille Syndrome in 92 Patients: Frequency and Relation to Prognosis

    Features of Alagille Syndrome in 92 Patients: Frequency and Relation to Prognosis by Karan M. Emerick, Elizabeth B. Rand, Elizabeth Goldmuntz, Ian D. Krantz, Nancy B. Spinner, David A. Piccoli

    Published 1999
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  13. 13
    Jagged1 mutations in Alagille syndrome

    Jagged1 mutations in Alagille syndrome by Nancy B. Spinner, Raymond P. Colliton, C�cile Crosnier, Ian D. Krantz, Michelle Hadchouel, M Meunier-Rotival

    Published 2000
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  14. 14
    Spectrum and Frequency of Jagged1 (JAG1) Mutations in Alagille Syndrome Patients and Their Families

    Spectrum and Frequency of Jagged1 (JAG1) Mutations in Alagille Syndrome Patients and Their Families by Ian D. Krantz, Raymond P. Colliton, Anna Genin, Elizabeth B. Rand, Linheng Li, David A. Piccoli, Nancy B. Spinner

    Published 1998
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  15. 15
    Analysis of Cardiovascular Phenotype and Genotype-Phenotype Correlation in Individuals With a <i>JAG1</i> Mutation and/or Alagille Syndrome

    Analysis of Cardiovascular Phenotype and Genotype-Phenotype Correlation in Individuals With a <i>JAG1</i> Mutation and/or Alagille Syndrome by Doff B. McElhinney, Ian D. Krantz, Lynn Bason, David A. Piccoli, Karan M. Emerick, Nancy B. Spinner, Elizabeth Goldmuntz

    Published 2002
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  16. 16
    Vascular Anomalies in Alagille Syndrome

    Vascular Anomalies in Alagille Syndrome by Binita M. Kamath, Nancy B. Spinner, Karan M. Emerick, Albert E. Chudley, Carol Booth, David A. Piccoli, Ian D. Krantz

    Published 2004
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  17. 17
    Jagged1 mutations in patients ascertained with isolated congenital heart defects

    Jagged1 mutations in patients ascertained with isolated congenital heart defects by Ian D. Krantz, Rosemarie Smith, Ray P. Colliton, Hilary Tinkel, Elaine H. Zackai, David A. Piccoli, Elizabeth Goldmuntz, Nancy B. Spinner

    Published 1999
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  18. 18
    Precocious sister chromatid separation (PSCS) in Cornelia de Lange syndrome

    Precocious sister chromatid separation (PSCS) in Cornelia de Lange syndrome by Maninder Kaur, Cheryl DeScipio, Jennifer McCallum, Dinah Yaeger, Marcella Devoto, Laird G. Jackson, Nancy B. Spinner, Ian D. Krantz

    Published 2005
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  19. 19
    Intracranial Vascular Abnormalities in Patients with Alagille Syndrome

    Intracranial Vascular Abnormalities in Patients with Alagille Syndrome by Karan M. Emerick, Ian D. Krantz, Binita M. Kamath, Crystal F. Darling, Delilah Burrowes, Nancy B. Spinner, Peter F. Whitington, David A. Piccoli

    Published 2005
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  20. 20
    NOTCH2 Mutations Cause Alagille Syndrome, a Heterogeneous Disorder of the Notch Signaling Pathway

    NOTCH2 Mutations Cause Alagille Syndrome, a Heterogeneous Disorder of the Notch Signaling Pathway by Ryan M. McDaniell, Daniel M. Warthen, Pedro A. Sanchez‐Lara, Athma A. Pai, Ian D. Krantz, David A. Piccoli, Nancy B. Spinner

    Published 2006
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