Morphometric analysis of untreated adult skulls in syndromic and nonsyndromic craniosynostosis

A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome.

Maximilian Muenke, Karen W. Gripp, Donna M. McDonald‐McGinn et al. · PubMed · 1997 · 394 citations

Dentistry, Genetics, Molecular Genetics +16

Intracranial Pressure and Intracranial Volume in Children with Craniosynostosis

David Gault, Dominique Rénier, Daniel Marchac et al. · Plastic & Reconstructive Surgery · 1992 · 308 citations

Medicine, Pediatrics, Craniofacial Development +12

Principles and practice of pediatric neurosurgery

Mario Giordano · Child s Nervous System · 2015 · 260 citations · Full text

Medicine, Neurological Surgery, Neurosurgery +12

Genetic Heterogeneity of Saethre-Chotzen Syndrome, Due to TWIST and FGFR Mutations

William A. Paznekas, Michael L. Cunningham, Timothy D. Howard et al. · The American Journal of Human Genetics · 1998 · 221 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Intracranial venous sinus hypertension: cause or consequence of hydrocephalus in infants?

Christian Sainte‐Rose, Jacques Lacombe, Alain Pierre‐Kahn et al. · Journal of neurosurgery · 1984 · 207 citations

Medicine, Neurosurgery, Pediatrics +13