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Publications by Nancy Bettina Spinner
NOTCH2mutations in Alagille Syndrome
Journal of Medical Genetics
Genetics
Related publications
Alagille Syndrome: Family Studies.
Journal of Medical Genetics
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ALAGILLE SYNDROME AS a CHALLENGING CLINICAL CASE IN PEDIATRIC PRACTICE (Case Report)
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A New Model of Alagille Syndrome With Broad Phenotypic Representation
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Hepatology
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Extracranial and Intracranial Vasculopathy With “Moyamoya Phenomenon” in Association With Alagille Syndrome
Frontiers in Neurology
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Novel Heterozygous Mutations in JAG1 and NOTCH2 Genes in a Neonatal Patient With Alagille Syndrome
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Critical Region in 2q31.2q32.3 Deletion Syndrome: Report of Two Phenotypically Distinct Patients, One With an Additional Deletion in Alagille Syndrome Region
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An Autosomal Recessive Form of Alagille-Like Syndrome That Is Not Linked to JAG1
Genetics in Medicine
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SR-BI- And ABCA1-mediated Cholesterol Efflux to Serum From Patients With Alagille Syndrome
Journal of Lipid Research
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Endocrinology
Cell Biology
DoUble Resin Casting Micro Computed Tomography (DUCT) Reveals Biliary and Vascular Pathology in a Mouse Model of Alagille Syndrome
