Pfeiffer Syndrome: Top KOLs in the world #1 M Michael Cohen Department of Pediatrics, Faculty of Medicine, Dalhousie Uni star star star star star Known for Ataxia Telangiectasia | Publication Abnormalities | Prenatal Diagnosis | Birth Prevalence | Apert Syndrome
#2 Maximilian Muenke National Human Genome Research Institute, National Institute star star star star star Known for Fibroblast Growth Factor | Holoprosencephaly Hpe | Sonic Hedgehog | Diverse Populations | Muenke Syndrome
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#3 Elaine H Zackai Department of Pediatrics, Perelman School of Medicine at the star star star star star_half Known for Human Pair | Deletion Syndrome | Situ Hybridization | Fibroblast Growth Factor | Intellectual Disability
#4 Richard David Hayward UCL Great Ormond Street Institute of Child Health, WC1N 1EH, star star star star star_half Known for Apert Syndrome | Fibroblast Growth Factor | Syndromic Craniosynostosis | Monobloc Distraction | Intracranial Pressure
#5 Barry M Jones London and Oxford, United Kingdom. | From the Departments of star star star star star_border Known for Fibroblast Growth Factor | Crouzon Syndrome | Cervical Spine | Syndromic Craniosynostosis | Intracranial Pressure
#6 Robin M Winter Genes, Development and Disease Theme, Institute of Child Hea star star star star star_border Known for Short Stature | Cleft Palate | Mental Retardation | Crouzon Syndrome | Fibroblast Growth Factor
#7 Andrew O M Wilkie MRC Weatherall Institute of Molecular Medicine, University o star star star star star_border Known for Apert Syndrome | Intracranial Hypertension | Type 2 Receptors | Fgfr2 Mutations | Fibroblast Growth Factor
#8 R A Pfeiffer Institut für Humangenetik, Friedrich-Alexander Universität E star star star star star_border Known for Long Arm | Fourier Transform Integrals | Partial Trisomy | Chromosome s Human | Hearing Loss
#9 William Reardon National Centre for Medical Genetics, Our Lady's Children's star star star star star_border Known for Pds Gene | Human Pair | Pendred Syndrome | Myotonic Dystrophy | Fibroblast Growth Factor
#10 Paul Rutland Genetics and Genomic Medicine, UCL Institute of Child Health star star star star star_border Known for Type 2 Receptors | Immunoglobulin Domain | Prenatal Diagnosis | Fibroblast Growth Factor | Crouzon Syndrome
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Recently Asked Questions
Refeeding Syndrome Refeeding syndrome is a life-threatening condition caused by the reintroduction of food in severely malnourished individuals. It is characterized by an...
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,...