CRELD1 mutations contribute to the occurrence of cardiac atrioventricular septal defects in Down syndrome [1]

Cheryl Maslen, Darcie Babcock, Susan W. Robinson, Lora J H Bean, Kenneth J. Dooley, Virginia L. Willour, Stephanie L. Sherman

    Research output: Contribution to journalArticle

    51 Citations (Scopus)
    Original languageEnglish (US)
    Pages (from-to)2501-2505
    Number of pages5
    JournalAmerican Journal of Medical Genetics, Part A
    Volume140
    Issue number22
    DOIs
    StatePublished - Nov 15 2006

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    Molecular Sequence Data
    Heart Septal Defects
    Amino Acid Sequence Homology
    Extracellular Matrix Proteins
    Genetic Models
    Cell Adhesion Molecules
    Amino Acid Substitution
    Down Syndrome
    Tertiary Protein Structure
    Point Mutation
    Amino Acid Sequence
    Exons
    Mutation
    Atrioventricular Septal Defect

    ASJC Scopus subject areas

    • Genetics(clinical)

    Cite this

    CRELD1 mutations contribute to the occurrence of cardiac atrioventricular septal defects in Down syndrome [1]. / Maslen, Cheryl; Babcock, Darcie; Robinson, Susan W.; Bean, Lora J H; Dooley, Kenneth J.; Willour, Virginia L.; Sherman, Stephanie L.

    In: American Journal of Medical Genetics, Part A, Vol. 140, No. 22, 15.11.2006, p. 2501-2505.

    Research output: Contribution to journalArticle

    Maslen, Cheryl ; Babcock, Darcie ; Robinson, Susan W. ; Bean, Lora J H ; Dooley, Kenneth J. ; Willour, Virginia L. ; Sherman, Stephanie L. / CRELD1 mutations contribute to the occurrence of cardiac atrioventricular septal defects in Down syndrome [1]. In: American Journal of Medical Genetics, Part A. 2006 ; Vol. 140, No. 22. pp. 2501-2505.
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