000 | 01840 a2200541 4500 | ||
---|---|---|---|
005 | 20250514000134.0 | ||
264 | 0 | _c20010927 | |
008 | 200109s 0 0 eng d | ||
022 | _a1098-3600 | ||
024 | 7 |
_a10.1097/00125817-200101000-00010 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aMarino, B | |
245 | 0 | 0 |
_aAnatomic patterns of conotruncal defects associated with deletion 22q11. _h[electronic resource] |
260 |
_bGenetics in medicine : official journal of the American College of Medical Genetics _c |
||
300 |
_a45-8 p. _bdigital |
||
500 | _aPublication Type: Journal Article | ||
650 | 0 | 4 |
_aAbnormalities, Multiple _xgenetics |
650 | 0 | 4 | _aAdolescent |
650 | 0 | 4 |
_aAorta, Thoracic _xabnormalities |
650 | 0 | 4 | _aChild |
650 | 0 | 4 | _aChild, Preschool |
650 | 0 | 4 | _aChromosome Deletion |
650 | 0 | 4 | _aChromosomes, Human, Pair 22 |
650 | 0 | 4 |
_aDiGeorge Syndrome _xdiagnosis |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 | _aGenotype |
650 | 0 | 4 |
_aHeart Defects, Congenital _xdiagnosis |
650 | 0 | 4 |
_aHeart Septal Defects, Ventricular _xdiagnosis |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aIn Situ Hybridization, Fluorescence |
650 | 0 | 4 | _aInfant |
650 | 0 | 4 | _aInfant, Newborn |
650 | 0 | 4 | _aMale |
650 | 0 | 4 | _aPhenotype |
650 | 0 | 4 |
_aPulmonary Atresia _xdiagnosis |
650 | 0 | 4 |
_aTetralogy of Fallot _xdiagnosis |
650 | 0 | 4 |
_aTruncus Arteriosus _xabnormalities |
700 | 1 | _aDigilio, M C | |
700 | 1 | _aToscano, A | |
700 | 1 | _aAnaclerio, S | |
700 | 1 | _aGiannotti, A | |
700 | 1 | _aFeltri, C | |
700 | 1 | _ade Ioris, M A | |
700 | 1 | _aAngioni, A | |
700 | 1 | _aDallapiccola, B | |
773 | 0 |
_tGenetics in medicine : official journal of the American College of Medical Genetics _gvol. 3 _gno. 1 _gp. 45-8 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1097/00125817-200101000-00010 _zAvailable from publisher's website |
999 |
_c11272395 _d11272395 |