000 01424 a2200445 4500
005 20250515022343.0
264 0 _c20060710
008 200607s 0 0 eng d
022 _a1552-4825
024 7 _a10.1002/ajmg.a.31210
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aSelicorni, A
245 0 0 _aThyroid anomalies in Williams syndrome: investigation of 95 patients.
_h[electronic resource]
260 _bAmerican journal of medical genetics. Part A
_cMay 2006
300 _a1098-101 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aMale
650 0 4 _aThyroid Diseases
_xblood
650 0 4 _aThyroid Function Tests
650 0 4 _aThyroid Gland
_xabnormalities
650 0 4 _aThyrotropin
_xblood
650 0 4 _aThyroxine
_xblood
650 0 4 _aTriiodothyronine
_xblood
650 0 4 _aUltrasonography
650 0 4 _aWilliams Syndrome
_xcomplications
700 1 _aFratoni, A
700 1 _aPavesi, M A
700 1 _aBottigelli, M
700 1 _aArnaboldi, E
700 1 _aMilani, D
773 0 _tAmerican journal of medical genetics. Part A
_gvol. 140
_gno. 10
_gp. 1098-101
856 4 0 _uhttps://doi.org/10.1002/ajmg.a.31210
_zAvailable from publisher's website
999 _c16202472
_d16202472