| 000 | 01223 a2200337 4500 | ||
|---|---|---|---|
| 005 | 20250518003447.0 | ||
| 264 | 0 | _c20190725 | |
| 008 | 201907s 0 0 eng d | ||
| 022 | _a1755-8794 | ||
| 024 | 7 |
_a10.1186/s12920-018-0410-6 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aKaseniit, Kristjan Eerik | |
| 245 | 0 | 0 |
_aStrategies to minimize false positives and interpret novel microdeletions based on maternal copy-number variants in 87,000 noninvasive prenatal screens. _h[electronic resource] |
| 260 |
_bBMC medical genomics _cOct 2018 |
||
| 300 |
_a90 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aDNA Copy Number Variations |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGene Deletion |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMaternal Serum Screening Tests |
| 650 | 0 | 4 | _aPregnancy |
| 650 | 0 | 4 |
_aPrenatal Diagnosis _xmethods |
| 650 | 0 | 4 | _aWhole Genome Sequencing |
| 700 | 1 | _aHogan, Gregory J | |
| 700 | 1 | _aD'Auria, Kevin M | |
| 700 | 1 | _aHaverty, Carrie | |
| 700 | 1 | _aMuzzey, Dale | |
| 773 | 0 |
_tBMC medical genomics _gvol. 11 _gno. 1 _gp. 90 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1186/s12920-018-0410-6 _zAvailable from publisher's website |
| 999 |
_c28958178 _d28958178 |
||