Potter Sequence

Potter Sequence is a congenital developmental anomaly characterized by a specific pattern of physical deformities resulting from chronic oligohydramnios, primarily due to bilateral renal agenesis or severe bilateral renal dysplasia, which leads to diminished fetal urine production and impaired lung development.

27

Publications

804

Citations

123

Authors

47

Institutions

Publications per year

2017–2026

3

Variants

Potter SyndromePotter's SequencePotter's Syndrome

Authors

123

  1. KV
    Kamiel Vandenberghe

    KU Leuven, Belgium

    2 publications · 70 citations

    2

    h-index

  2. JF
    James F. Reynolds

    Duke University, United States

    2 publications · 77 citations

    2

    h-index

  3. JM
    John M. Opitz

    University of Wisconsin–Madison, United States

    2 publications · 77 citations

    2

    h-index

  4. JP
    J. P. Fryns

    KU Leuven, Belgium

    2 publications · 70 citations

    2

    h-index

  5. DE
    Dennis E. Bulman

    University of Ottawa, Canada

    1 publications · 16 citations

    1

    h-index

1–5 of 123

Venues

  1. American Journal of Medical Genetics

    7 publications · 246 citations

    7

    h-index

  2. PubMed

    Repository · 3 publications · 53 citations

    3

    h-index

  3. American Journal of Medical Genetics Part A

    2 publications · 43 citations

    2

    h-index

  4. Journal of Archaeological Method and Theory

    1 publications · 28 citations

    1

    h-index

  5. PLoS ONE

    1 publications · 44 citations

    1

    h-index

1–5