| 000 | 01743 a2200589 4500 | ||
|---|---|---|---|
| 005 | 20250518101415.0 | ||
| 264 | 0 | _c20211004 | |
| 008 | 202110s 0 0 eng d | ||
| 022 | _a1720-8386 | ||
| 024 | 7 |
_a10.1007/s40618-020-01271-z _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aElmougy, F | |
| 245 | 0 | 0 |
_aGenetic profiling of CAH Egyptian children: rapid guide to clinical interpretation of common mutations. _h[electronic resource] |
| 260 |
_bJournal of endocrinological investigation _cJan 2021 |
||
| 300 |
_a83-93 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article | ||
| 650 | 0 | 4 |
_aAdrenal Hyperplasia, Congenital _xepidemiology |
| 650 | 0 | 4 |
_aBiomarkers _xanalysis |
| 650 | 0 | 4 | _aCase-Control Studies |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aCohort Studies |
| 650 | 0 | 4 |
_aEgypt _xepidemiology |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aFollow-Up Studies |
| 650 | 0 | 4 |
_aGenetic Testing _xmethods |
| 650 | 0 | 4 | _aGenotype |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aPrognosis |
| 650 | 0 | 4 |
_aSteroid 21-Hydroxylase _xgenetics |
| 700 | 1 | _aElsharkawy, M | |
| 700 | 1 | _aHafez, M | |
| 700 | 1 | _aAtty, S A | |
| 700 | 1 | _aBaz, H | |
| 700 | 1 | _aIbrahim, A | |
| 700 | 1 | _aSoliman, H | |
| 700 | 1 | _aEkladious, S | |
| 700 | 1 | _aAbdullatif, M | |
| 700 | 1 | _aThabet, G | |
| 700 | 1 | _aRady, N | |
| 700 | 1 | _aAfif, A | |
| 700 | 1 | _aTolba, A | |
| 700 | 1 | _aZaki, Z | |
| 700 | 1 | _aMusa, N | |
| 773 | 0 |
_tJournal of endocrinological investigation _gvol. 44 _gno. 1 _gp. 83-93 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1007/s40618-020-01271-z _zAvailable from publisher's website |
| 999 |
_c30924339 _d30924339 |
||