| 000 | 01627 a2200493 4500 | ||
|---|---|---|---|
| 005 | 20250516113222.0 | ||
| 264 | 0 | _c20130430 | |
| 008 | 201304s 0 0 eng d | ||
| 022 | _a1097-0223 | ||
| 024 | 7 |
_a10.1002/pd.3977 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aLiao, Jun | |
| 245 | 0 | 0 |
_aPrenatal detection of del(10)(q11.2) mosaicism in chorionic villus specimens likely caused by a common chromosomal fragile site FRA10G is associated with a normal phenotype. _h[electronic resource] |
| 260 |
_bPrenatal diagnosis _cDec 2012 |
||
| 300 |
_a1166-9 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article | ||
| 650 | 0 | 4 | _aCells, Cultured |
| 650 | 0 | 4 | _aChorionic Villi Sampling |
| 650 | 0 | 4 | _aChromosome Deletion |
| 650 | 0 | 4 |
_aChromosome Disorders _xdiagnosis |
| 650 | 0 | 4 |
_aChromosome Fragile Sites _xgenetics |
| 650 | 0 | 4 | _aChromosomes, Human, Pair 10 |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 | _aKaryotyping |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMosaicism |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aPregnancy |
| 650 | 0 | 4 |
_aPregnancy Outcome _xepidemiology |
| 650 | 0 | 4 |
_aPregnancy Trimester, First _xgenetics |
| 650 | 0 | 4 |
_aPrenatal Diagnosis _xmethods |
| 650 | 0 | 4 | _aPrevalence |
| 700 | 1 | _aSathanoori, Malini | |
| 700 | 1 | _aYatsenko, Svetlana A | |
| 700 | 1 | _aHu, Jie | |
| 700 | 1 | _aKochmar, Sally J | |
| 700 | 1 | _aHoffner, Lori | |
| 700 | 1 | _aHogge, W Allen | |
| 700 | 1 | _aSurti, Urvashi | |
| 773 | 0 |
_tPrenatal diagnosis _gvol. 32 _gno. 12 _gp. 1166-9 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/pd.3977 _zAvailable from publisher's website |
| 999 |
_c22138660 _d22138660 |
||