000 01220 a2200337 4500
005 20250512035816.0
264 0 _c19890323
008 198903s 0 0 eng d
022 _a1040-3787
024 7 _a10.1002/ajmg.1320250627
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aKardon, N B
245 0 0 _aTwo sporadic cases of amelia/phocomelia with similar phenotype: rare and unusually symmetrical form of FFU dysostosis or separate entity?
_h[electronic resource]
260 _bAmerican journal of medical genetics. Supplement
_c1986
300 _a239-45 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aEctromelia
_xclassification
650 0 4 _aFemur
_xabnormalities
650 0 4 _aFibula
_xabnormalities
650 0 4 _aHumans
650 0 4 _aInfant, Newborn
650 0 4 _aMale
650 0 4 _aRadiography
650 0 4 _aSyndrome
650 0 4 _aUlna
_xabnormalities
700 1 _aDana, L P
700 1 _aFitzGerald, J M
700 1 _aOpitz, J M
773 0 _tAmerican journal of medical genetics. Supplement
_gvol. 2
_gp. 239-45
856 4 0 _uhttps://doi.org/10.1002/ajmg.1320250627
_zAvailable from publisher's website
999 _c3152092
_d3152092