| 000 | 01571 a2200493 4500 | ||
|---|---|---|---|
| 005 | 20250516002122.0 | ||
| 264 | 0 | _c20110210 | |
| 008 | 201102s 0 0 eng d | ||
| 022 | _a1421-9964 | ||
| 024 | 7 |
_a10.1159/000317012 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aAnselem, O | |
| 245 | 0 | 0 |
_aPrenatal diagnosis of 18q-syndrome: a case of fetal mosaicism with a normal karyotype in chorionic villi. _h[electronic resource] |
| 260 |
_bFetal diagnosis and therapy _c2010 |
||
| 300 |
_a180-5 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aAmniocentesis |
| 650 | 0 | 4 |
_aChorionic Villi _xultrastructure |
| 650 | 0 | 4 | _aChorionic Villi Sampling |
| 650 | 0 | 4 | _aChromosome Deletion |
| 650 | 0 | 4 |
_aChromosome Disorders _xdiagnosis |
| 650 | 0 | 4 |
_aChromosomes, Human, Pair 18 _xdiagnostic imaging |
| 650 | 0 | 4 |
_aCorpus Callosum _xdiagnostic imaging |
| 650 | 0 | 4 | _aFalse Negative Reactions |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aFetal Development |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aKaryotyping |
| 650 | 0 | 4 | _aMosaicism |
| 650 | 0 | 4 | _aPregnancy |
| 650 | 0 | 4 | _aPrenatal Diagnosis |
| 650 | 0 | 4 | _aStillbirth |
| 650 | 0 | 4 | _aUltrasonography, Prenatal |
| 700 | 1 | _aBazin, A | |
| 700 | 1 | _aMechler, C | |
| 700 | 1 | _aBlin, G | |
| 700 | 1 | _aGarel, C | |
| 700 | 1 | _aAboura, A | |
| 700 | 1 | _aMoutard, M-L | |
| 700 | 1 | _aMandelbrot, L | |
| 773 | 0 |
_tFetal diagnosis and therapy _gvol. 28 _gno. 3 _gp. 180-5 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1159/000317012 _zAvailable from publisher's website |
| 999 |
_c20161758 _d20161758 |
||