Canlyniadau Chwilio - Nancy B. Spinner

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  1. 1
    Alagille Syndrome: Genetics and Functional Models

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

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

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

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

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

    Cyhoeddwyd 2015
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  4. 4
    Alagille syndrome.

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

    Cyhoeddwyd 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 gan Peter Ordentlich, Michael Downes, Wen Xie, Anna Genin, Nancy B. Spinner, Ronald M. Evans

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

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

    Cyhoeddwyd 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 gan Ahmad Abou Tayoun, Nancy B. Spinner, Heidi L. Rehm, Robert C. Green, Diana W. Bianchi

    Cyhoeddwyd 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 gan Marian Reiff, Ellen Giarelli, Barbara A. Bernhardt, Ebony Easley, Nancy B. Spinner, Pamela Sankar, Surabhi Mulchandani

    Cyhoeddwyd 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 gan Gerard T. Berry, John Mallee, H. Moo Kwon, Jong S. Rim, Wadia R. Mulla, Maximilian Muenke, Nancy B. Spinner

    Cyhoeddwyd 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 gan Adam J. Kaye, Elizabeth B. Rand, Pedro S Munoz, Nancy B. Spinner, Alan W. Flake, Binita M. Kamath

    Cyhoeddwyd 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 gan Marian Reiff, Barbara A. Bernhardt, Surabhi Mulchandani, Danielle Soucier, Diana Cornell, Reed E. Pyeritz, Nancy B. Spinner

    Cyhoeddwyd 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 gan Karan M. Emerick, Elizabeth B. Rand, Elizabeth Goldmuntz, Ian D. Krantz, Nancy B. Spinner, David A. Piccoli

    Cyhoeddwyd 1999
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  13. 13
    Jagged1 mutations in Alagille syndrome

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

    Cyhoeddwyd 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 gan Ian D. Krantz, Raymond P. Colliton, Anna Genin, Elizabeth B. Rand, Linheng Li, David A. Piccoli, Nancy B. Spinner

    Cyhoeddwyd 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 gan Doff B. McElhinney, Ian D. Krantz, Lynn Bason, David A. Piccoli, Karan M. Emerick, Nancy B. Spinner, Elizabeth Goldmuntz

    Cyhoeddwyd 2002
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  16. 16
    Vascular Anomalies in Alagille Syndrome

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

    Cyhoeddwyd 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 gan Ian D. Krantz, Rosemarie Smith, Ray P. Colliton, Hilary Tinkel, Elaine H. Zackai, David A. Piccoli, Elizabeth Goldmuntz, Nancy B. Spinner

    Cyhoeddwyd 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 gan Maninder Kaur, Cheryl DeScipio, Jennifer McCallum, Dinah Yaeger, Marcella Devoto, Laird G. Jackson, Nancy B. Spinner, Ian D. Krantz

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

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

    Cyhoeddwyd 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 gan Ryan M. McDaniell, Daniel M. Warthen, Pedro A. Sanchez‐Lara, Athma A. Pai, Ian D. Krantz, David A. Piccoli, Nancy B. Spinner

    Cyhoeddwyd 2006
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