• KOL
  • Pfeiffer Syndrome
  • Pfeiffer Syndrome



    Pfeiffer Syndrome: Top KOLs in the world

    M Michael Cohen #1
    M Michael Cohen
    Department of Pediatrics, Faculty of Medicine, Dalhousie Uni
    Known for Ataxia Telangiectasia | Publication Abnormalities | Prenatal Diagnosis | Birth Prevalence | Apert Syndrome
    Maximilian Muenke #2
    Maximilian Muenke
    National Human Genome Research Institute, National Institute
    Known for Fibroblast Growth Factor | Holoprosencephaly Hpe | Sonic Hedgehog | Diverse Populations | Muenke Syndrome

    Elaine H Zackai #3
    Elaine H Zackai
    Department of Pediatrics, Perelman School of Medicine at the
    Known for Human Pair | Deletion Syndrome | Situ Hybridization | Fibroblast Growth Factor | Intellectual Disability
    Richard David Hayward #4
    Richard David Hayward
    UCL Great Ormond Street Institute of Child Health, WC1N 1EH,
    Known for Apert Syndrome | Fibroblast Growth Factor | Syndromic Craniosynostosis | Monobloc Distraction | Intracranial Pressure
    Barry M Jones #5
    Barry M Jones
    London and Oxford, United Kingdom. | From the Departments of
    Known for Fibroblast Growth Factor | Crouzon Syndrome | Cervical Spine | Syndromic Craniosynostosis | Intracranial Pressure
    Robin M Winter #6
    Robin M Winter
    Genes, Development and Disease Theme, Institute of Child Hea
    Known for Short Stature | Cleft Palate | Mental Retardation | Crouzon Syndrome | Fibroblast Growth Factor
    Andrew O M Wilkie #7
    Andrew O M Wilkie
    MRC Weatherall Institute of Molecular Medicine, University o
    Known for Apert Syndrome | Intracranial Hypertension | Type 2 Receptors | Fgfr2 Mutations | Fibroblast Growth Factor
    R A Pfeiffer #8
    R A Pfeiffer
    Institut für Humangenetik, Friedrich-Alexander Universität E
    Known for Long Arm | Fourier Transform Integrals | Partial Trisomy | Chromosomes Human | Hearing Loss
    William Reardon #9
    William Reardon
    National Centre for Medical Genetics, Our Lady's Children's
    Known for Pds Gene | Human Pair | Pendred Syndrome | Myotonic Dystrophy | Fibroblast Growth Factor
    Paul Rutland #10
    Paul Rutland
    Genetics and Genomic Medicine, UCL Institute of Child Health
    Known for Type 2 Receptors | Immunoglobulin Domain | Prenatal Diagnosis | Fibroblast Growth Factor | Crouzon Syndrome

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    Recently Asked Questions

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    Pfeiffer Syndrome Pfeiffer syndrome is a rare genetic disorder that affects the bones and skull. It is characterized by an abnormal fusion of certain bones in the skull,...