000 | 01359 a2200397 4500 | ||
---|---|---|---|
005 | 20250513211044.0 | ||
264 | 0 | _c20000606 | |
008 | 200006s 0 0 eng d | ||
022 | _a1328-8067 | ||
024 | 7 |
_a10.1046/j.1442-200x.2000.01183.x _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aAkiba, T | |
245 | 0 | 0 |
_aThree patients with different phenotypes in a family with chromosome 22q11.2 deletions. _h[electronic resource] |
260 |
_bPediatrics international : official journal of the Japan Pediatric Society _cApr 2000 |
||
300 |
_a183-5 p. _bdigital |
||
500 | _aPublication Type: Case Reports; Journal Article | ||
650 | 0 | 4 | _aAdult |
650 | 0 | 4 | _aChild, Preschool |
650 | 0 | 4 |
_aChromosomes, Human, Pair 22 _xgenetics |
650 | 0 | 4 |
_aDuctus Arteriosus, Patent _xgenetics |
650 | 0 | 4 |
_aFacial Asymmetry _xgenetics |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 | _aGene Deletion |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aInfant |
650 | 0 | 4 | _aMale |
650 | 0 | 4 | _aPedigree |
650 | 0 | 4 | _aPhenotype |
700 | 1 | _aOdake, A | |
700 | 1 | _aShirahata, E | |
700 | 1 | _aMatsunaga, A | |
700 | 1 | _aSakamoto, M | |
700 | 1 | _aYazaki, N | |
773 | 0 |
_tPediatrics international : official journal of the Japan Pediatric Society _gvol. 42 _gno. 2 _gp. 183-5 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1046/j.1442-200x.2000.01183.x _zAvailable from publisher's website |
999 |
_c10756617 _d10756617 |