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 |