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    3 research outputs found

    Congenital Central Hypothyroidism due to a Homozygous Mutation in the Thyrotropin β-Subunit Gene Follows an Autosomal Recessive Inheritance

    Author
    Publication venue
    'The Endocrine Society'
    Publication date
    Field of study
    No full text

    A heterozygous mutation of the IGF-1 receptor causes retention of the nascent protein in the endoplasmic reticulum and results in intrauterine and postnatal growth retardation

    Author
    Publication venue
    'S. Karger AG'
    Publication date
    Field of study
    No full text

    A heterozygous mutation of the IGF-1 receptor causes retention of the nascent protein in the endoplasmic reticulum and results in intrauterine and postnatal growth retardation

    Author
    Publication venue
    'S. Karger AG'
    Publication date
    Field of study
    No full text
    Publikationsserver der RWTH Aachen University
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