| 000 | 01831 a2200541 4500 | ||
|---|---|---|---|
| 005 | 20250514023752.0 | ||
| 264 | 0 | _c20020329 | |
| 008 | 200203s 0 0 fre d | ||
| 022 | _a0003-4266 | ||
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aDerrien, C | |
| 245 | 0 | 0 |
_a[Pseudohypoparathyroidism or hypoparathyroidism? A misleading clinical presentation]. _h[electronic resource] |
| 260 |
_bAnnales d'endocrinologie _cDec 2001 |
||
| 300 |
_a529-33 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; English Abstract; Journal Article | ||
| 650 | 0 | 4 |
_aAbnormalities, Multiple _xgenetics |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aChromosome Deletion |
| 650 | 0 | 4 |
_aChromosome Disorders _xdiagnosis |
| 650 | 0 | 4 |
_aChromosomes, Human, Pair 22 _xultrastructure |
| 650 | 0 | 4 | _aDiagnosis, Differential |
| 650 | 0 | 4 |
_aFace _xabnormalities |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aFibrous Dysplasia, Polyostotic _xdiagnosis |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aHypercalcemia _xcongenital |
| 650 | 0 | 4 |
_aHypoparathyroidism _xdiagnosis |
| 650 | 0 | 4 | _aIn Situ Hybridization, Fluorescence |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 |
_aIntellectual Disability _xetiology |
| 650 | 0 | 4 |
_aObesity _xetiology |
| 650 | 0 | 4 |
_aParathyroid Hormone _xdeficiency |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 |
_aPhosphorus _xblood |
| 650 | 0 | 4 | _aPregnancy |
| 650 | 0 | 4 |
_aPregnancy Complications _xdiagnosis |
| 650 | 0 | 4 |
_aPseudohypoparathyroidism _xdiagnosis |
| 650 | 0 | 4 |
_aPurpura, Thrombocytopenic, Idiopathic _xcomplications |
| 650 | 0 | 4 |
_aScoliosis _xetiology |
| 650 | 0 | 4 | _aSyndrome |
| 650 | 0 | 4 |
_aVelopharyngeal Insufficiency _xetiology |
| 700 | 1 | _aOdent, S | |
| 700 | 1 | _aHenry, C | |
| 700 | 1 | _aDe La Villemarque, R | |
| 700 | 1 | _aPoirier, J Y | |
| 700 | 1 | _aMaugendre, D | |
| 773 | 0 |
_tAnnales d'endocrinologie _gvol. 62 _gno. 6 _gp. 529-33 |
|
| 999 |
_c11753686 _d11753686 |
||