Two sporadic cases of amelia/phocomelia with similar phenotype: rare and unusually symmetrical form of FFU dysostosis or separate entity?

Kardon, N B

Two sporadic cases of amelia/phocomelia with similar phenotype: rare and unusually symmetrical form of FFU dysostosis or separate entity? [electronic resource] - American journal of medical genetics. Supplement 1986 - 239-45 p. digital

Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

1040-3787

10.1002/ajmg.1320250627 doi


Ectromelia--classification
Femur--abnormalities
Fibula--abnormalities
Humans
Infant, Newborn
Male
Radiography
Syndrome
Ulna--abnormalities