gjf003

George J. Feldman, PhD, DMD

Contact Dr. Feldman

1015 Walnut Street
Curtis Building, Room 501
Philadelphia, PA 19107

(215) 955-5480

Most Recent Peer-reviewed Publications

  1. Response to "mutations of the Noggin and of the activin A type I receptor genes in fibrodysplasia ossificans progressiva (FOP)" by Lucotte et al
  2. Over-expression of BMP4 and BMP5 in a child with axial skeletal malformations and heterotopic ossification: A new syndrome
  3. Erratum: A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva (Nature Genetics (2006) 38, (525-527))
  4. A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva
  5. The genetics of fibrodysplasia ossificans progressiva
  6. Exoneration of NF-κB dysregulation in fibrodysplasia ossificans progressiva
  7. Fibrodysplasia ossificans progressiva, a heritable disorder of severe heterotopic ossification, maps to human chromosome 4q27-31
  8. Linkage exclusion and mutational analysis of the noggin gene in patients with fibrodysplasia ossificans progressiva (FOP)
  9. Erratum: Opiz G/BBB syndrome in Xp22: Mutations in the MID1 gene cluster in the carboxy-terminal domain (American Journal of Human Genetics (September 1998) 63 (703-710))
  10. Opitz G/BBB syndrome in Xp22: Mutations in the MID1 gene cluster in the carboxy-terminal domain
  11. A novel phenotypic pattern in X-linked inheritance: Craniofrontonasal syndrome maps to Xp22
  12. Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22
  13. Mutations in FGFR1 and FGFR2 cause familial and sporadic pfeiffer syndrome
  14. A gene for cleidocranial dysplasia maps to the short arm of chromosome 6
  15. Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2
  16. Reports: Linkage of pfeiffer syndrome to chromosome 8 centromere and evidence for genetic heterogeneity