| 000 | 01444 a2200445 4500 | ||
|---|---|---|---|
| 005 | 20250512091552.0 | ||
| 264 | 0 | _c19740919 | |
| 008 | 197409s 0 0 fre d | ||
| 022 | _a0003-9764 | ||
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aRochiccioli, P | |
| 245 | 0 | 0 |
_a[Thyroid hormonosynthesis disorders due to iodotyrosine-dehalogenase deficiency. Value of the D.I.T. test for the detection of heterozygotes]. _h[electronic resource] |
| 260 |
_bArchives francaises de pediatrie _cJan 1974 |
||
| 300 |
_a25-36 p. _bdigital |
||
| 500 | _aPublication Type: Clinical Trial; English Abstract; Journal Article | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aChromosome Aberrations |
| 650 | 0 | 4 | _aChromosome Disorders |
| 650 | 0 | 4 | _aClinical Trials as Topic |
| 650 | 0 | 4 | _aConsanguinity |
| 650 | 0 | 4 |
_aDiiodotyrosine _xurine |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenes, Recessive |
| 650 | 0 | 4 |
_aGoiter _xetiology |
| 650 | 0 | 4 | _aHeterozygote |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aHypothyroidism _xdiagnosis |
| 650 | 0 | 4 |
_aIodine _xmetabolism |
| 650 | 0 | 4 | _aIodine Radioisotopes |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMetabolism, Inborn Errors _xcomplications |
| 650 | 0 | 4 | _aMethods |
| 650 | 0 | 4 | _aThyroid Function Tests |
| 650 | 0 | 4 |
_aThyroid Hormones _xbiosynthesis |
| 700 | 1 | _aDutau, G | |
| 773 | 0 |
_tArchives francaises de pediatrie _gvol. 31 _gno. 1 _gp. 25-36 |
|
| 999 |
_c4141029 _d4141029 |
||