| 000 | 01465 a2200397 4500 | ||
|---|---|---|---|
| 005 | 20250513122241.0 | ||
| 264 | 0 | _c19970903 | |
| 008 | 199709s 0 0 eng d | ||
| 022 | _a0148-7299 | ||
| 024 | 7 |
_a10.1002/(sici)1096-8628(19970808)71:2<189::aid-ajmg13>3.0.co;2-a _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aStockton, D W | |
| 245 | 0 | 0 |
_aSevere clinical phenotype due to an interstitial deletion of the short arm of chromosome 1: a brief review. _h[electronic resource] |
| 260 |
_bAmerican journal of medical genetics _cAug 1997 |
||
| 300 |
_a189-93 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 |
_aAbnormalities, Multiple _xgenetics |
| 650 | 0 | 4 | _aChromosome Banding |
| 650 | 0 | 4 | _aChromosome Deletion |
| 650 | 0 | 4 |
_aChromosomes, Human, Pair 1 _xgenetics |
| 650 | 0 | 4 |
_aCraniofacial Abnormalities _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aHand Deformities, Congenital _xgenetics |
| 650 | 0 | 4 |
_aHeart Defects, Congenital _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 | _aKaryotyping |
| 650 | 0 | 4 | _aPhenotype |
| 700 | 1 | _aRoss, H L | |
| 700 | 1 | _aBacino, C A | |
| 700 | 1 | _aAltman, C A | |
| 700 | 1 | _aShaffer, L G | |
| 700 | 1 | _aLupski, J R | |
| 773 | 0 |
_tAmerican journal of medical genetics _gvol. 71 _gno. 2 _gp. 189-93 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/(sici)1096-8628(19970808)71:2<189::aid-ajmg13>3.0.co;2-a _zAvailable from publisher's website |
| 999 |
_c9197524 _d9197524 |
||