| 000 | 01369 a2200445 4500 | ||
|---|---|---|---|
| 005 | 20250513203411.0 | ||
| 264 | 0 | _c20000327 | |
| 008 | 200003s 0 0 eng d | ||
| 022 | _a0197-3851 | ||
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aLi, M M | |
| 245 | 0 | 0 |
_aCharacterization and clinical implications of marker chromosomes identified at prenatal diagnosis. _h[electronic resource] |
| 260 |
_bPrenatal diagnosis _cFeb 2000 |
||
| 300 |
_a138-43 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article | ||
| 650 | 0 | 4 | _aAmniocentesis |
| 650 | 0 | 4 | _aChromosome Aberrations |
| 650 | 0 | 4 | _aChromosomes, Human, Pair 12 |
| 650 | 0 | 4 | _aChromosomes, Human, Pair 15 |
| 650 | 0 | 4 | _aChromosomes, Human, Pair 18 |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenetic Markers |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aIn Situ Hybridization, Fluorescence |
| 650 | 0 | 4 | _aIsochromosomes |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aPregnancy |
| 650 | 0 | 4 | _aRNA, Long Noncoding |
| 650 | 0 | 4 | _aRNA, Untranslated |
| 650 | 0 | 4 | _aSex Chromosome Aberrations |
| 650 | 0 | 4 |
_aTranscription Factors _xgenetics |
| 650 | 0 | 4 |
_aTurner Syndrome _xdiagnosis |
| 650 | 0 | 4 | _aX Chromosome |
| 700 | 1 | _aHoward-Peebles, P N | |
| 700 | 1 | _aKillos, L D | |
| 700 | 1 | _aFallon, L | |
| 700 | 1 | _aListgarten, E | |
| 700 | 1 | _aStanley, W S | |
| 773 | 0 |
_tPrenatal diagnosis _gvol. 20 _gno. 2 _gp. 138-43 |
|
| 999 |
_c10648831 _d10648831 |
||