Craniofrontonasal dysplasia

This publication has 24 references indexed in Scilit:

• The central nervous system in the Apert syndrome
  American Journal of Medical Genetics, 1990
• Craniofrontonasal dysostosis with deafness and axillary pterygia
  American Journal of Medical Genetics, 1989
• Autosomal recessive acro‐fronto‐facio‐nasal dysostosis associated with genitourinary anomalies
  American Journal of Medical Genetics, 1989
• New autosomal dominant syndrome resembling craniofrontonasal dysplasia
  American Journal of Medical Genetics, 1987
• Delineation of the male phenotype in craniofrontonasal syndrome
  American Journal of Medical Genetics, 1987
• Congenital hypothalamic hamartoma associated with severe midline defect: A developmental field defect. Report of a case
  American Journal of Medical Genetics, 1986
• A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with fronto‐nasal dysostosis, cleft lip/palate, limb hypoplasia, and postaxial poly‐syndactyly: Acro‐fronto‐facio‐nasal dysostosis syndrome
  American Journal of Medical Genetics, 1985
• Frontonasal dysplasia, coronal cranisoynostosis, pre‐ and postaxial polydactyly and split nails: a new autosomal dominant mutant with reduced penetrance and varibale expression?
  Clinical Genetics, 1983
• Fronto-facio-nasal dysostosis - a new autosomal recessive syndrome
  American Journal of Medical Genetics, 1981
• Frontonasal dysplasia
  The Journal of Pediatrics, 1970