Baller Gerold syndrome and Fanconi anaemia

Am J Med Genet. 1998 Jan 13;75(2):228-9. doi: 10.1002/(sici)1096-8628(19980113)75:2<228::aid-ajmg25>3.0.co;2-q.
No abstract available

Publication types

  • Case Reports
  • Comment
  • Letter

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Chromosome Breakage
  • Consanguinity
  • Craniosynostoses / genetics
  • Fanconi Anemia / diagnosis
  • Fanconi Anemia / genetics*
  • Follow-Up Studies
  • Humans
  • Infant
  • Karyotyping
  • Male
  • Syndrome