| 000 | 01724 a2200481 4500 | ||
|---|---|---|---|
| 005 | 20250518004637.0 | ||
| 264 | 0 | _c20191029 | |
| 008 | 201910s 0 0 eng d | ||
| 022 | _a1552-4833 | ||
| 024 | 7 |
_a10.1002/ajmg.a.40641 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aAbu-El-Haija, Aya | |
| 245 | 0 | 0 |
_aTwo patients with FOXF1 mutations with alveolar capillary dysplasia with misalignment of pulmonary veins and other malformations: Two different presentations and outcomes. _h[electronic resource] |
| 260 |
_bAmerican journal of medical genetics. Part A _c12 2018 |
||
| 300 |
_a2877-2881 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 |
_aAbnormalities, Multiple _xdiagnosis |
| 650 | 0 | 4 | _aAutopsy |
| 650 | 0 | 4 | _aBiomarkers |
| 650 | 0 | 4 | _aBiopsy |
| 650 | 0 | 4 | _aComparative Genomic Hybridization |
| 650 | 0 | 4 | _aCytogenetic Analysis |
| 650 | 0 | 4 | _aEchocardiography |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aForkhead Transcription Factors _xgenetics |
| 650 | 0 | 4 | _aGenetic Association Studies |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 |
_aPersistent Fetal Circulation Syndrome _xdiagnosis |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aPolymorphism, Single Nucleotide |
| 650 | 0 | 4 |
_aPulmonary Alveoli _xabnormalities |
| 650 | 0 | 4 |
_aPulmonary Veins _xabnormalities |
| 700 | 1 | _aFineman, Jeff | |
| 700 | 1 | _aConnolly, Andrew J | |
| 700 | 1 | _aMurali, Priyanka | |
| 700 | 1 | _aJudge, Luke M | |
| 700 | 1 | _aSlavotinek, Anne M | |
| 773 | 0 |
_tAmerican journal of medical genetics. Part A _gvol. 176 _gno. 12 _gp. 2877-2881 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/ajmg.a.40641 _zAvailable from publisher's website |
| 999 |
_c28996887 _d28996887 |
||