| 000 | 01496 a2200421 4500 | ||
|---|---|---|---|
| 005 | 20250513094440.0 | ||
| 264 | 0 | _c19961009 | |
| 008 | 199610s 0 0 eng d | ||
| 022 | _a0148-7299 | ||
| 024 | 7 |
_a10.1002/(SICI)1096-8628(19960102)61:1<65::AID-AJMG12>3.0.CO;2-U _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aRossbach, H C | |
| 245 | 0 | 0 |
_aFanconi anemia in brothers initially diagnosed with VACTERL association with hydrocephalus, and subsequently with Baller-Gerold syndrome. _h[electronic resource] |
| 260 |
_bAmerican journal of medical genetics _cJan 1996 |
||
| 300 |
_a65-7 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 |
_aAbnormalities, Multiple _xdiagnosis |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 |
_aCraniosynostoses _xdiagnosis |
| 650 | 0 | 4 | _aCytogenetics |
| 650 | 0 | 4 | _aDiagnosis, Differential |
| 650 | 0 | 4 |
_aFanconi Anemia _xdiagnosis |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aHydrocephalus _xgenetics |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aNuclear Family |
| 650 | 0 | 4 |
_aRadius _xabnormalities |
| 650 | 0 | 4 | _aSyndrome |
| 700 | 1 | _aSutcliffe, M J | |
| 700 | 1 | _aHaag, M M | |
| 700 | 1 | _aGrana, N H | |
| 700 | 1 | _aRossi, A R | |
| 700 | 1 | _aBarbosa, J L | |
| 773 | 0 |
_tAmerican journal of medical genetics _gvol. 61 _gno. 1 _gp. 65-7 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/(SICI)1096-8628(19960102)61:1<65::AID-AJMG12>3.0.CO;2-U _zAvailable from publisher's website |
| 999 |
_c8738978 _d8738978 |
||