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