000 01359 a2200397 4500
005 20250513211044.0
264 0 _c20000606
008 200006s 0 0 eng d
022 _a1328-8067
024 7 _a10.1046/j.1442-200x.2000.01183.x
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aAkiba, T
245 0 0 _aThree patients with different phenotypes in a family with chromosome 22q11.2 deletions.
_h[electronic resource]
260 _bPediatrics international : official journal of the Japan Pediatric Society
_cApr 2000
300 _a183-5 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAdult
650 0 4 _aChild, Preschool
650 0 4 _aChromosomes, Human, Pair 22
_xgenetics
650 0 4 _aDuctus Arteriosus, Patent
_xgenetics
650 0 4 _aFacial Asymmetry
_xgenetics
650 0 4 _aFemale
650 0 4 _aGene Deletion
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aMale
650 0 4 _aPedigree
650 0 4 _aPhenotype
700 1 _aOdake, A
700 1 _aShirahata, E
700 1 _aMatsunaga, A
700 1 _aSakamoto, M
700 1 _aYazaki, N
773 0 _tPediatrics international : official journal of the Japan Pediatric Society
_gvol. 42
_gno. 2
_gp. 183-5
856 4 0 _uhttps://doi.org/10.1046/j.1442-200x.2000.01183.x
_zAvailable from publisher's website
999 _c10756617
_d10756617