| 000 | 01325 a2200373 4500 | ||
|---|---|---|---|
| 005 | 20250518044849.0 | ||
| 264 | 0 | _c20200608 | |
| 008 | 202006s 0 0 eng d | ||
| 022 | _a2046-1402 | ||
| 024 | 7 |
_a10.12688/f1000research.18455.1 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aKaya, Murat | |
| 245 | 0 | 0 |
_aCase Report: a novel chromosomal insertion, 46, XY, inv ins(18;2)(q11.2;q13q22), in a patient with infertility and mild intellectual disability. _h[electronic resource] |
| 260 |
_bF1000Research _c2019 |
||
| 300 |
_a281 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aChromosome Inversion |
| 650 | 0 | 4 |
_aChromosomes, Human, Pair 18 _xgenetics |
| 650 | 0 | 4 |
_aChromosomes, Human, Pair 2 _xgenetics |
| 650 | 0 | 4 | _aComparative Genomic Hybridization |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aInfertility, Male _xgenetics |
| 650 | 0 | 4 |
_aIntellectual Disability _xgenetics |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMutagenesis, Insertional |
| 700 | 1 | _aSuer, İlknur | |
| 700 | 1 | _aÖztürk, Şükrü | |
| 700 | 1 | _aÇefle, Kıvanç | |
| 700 | 1 | _aKaraman, Birsen | |
| 700 | 1 | _aPalanduz, Şükrü | |
| 773 | 0 |
_tF1000Research _gvol. 8 _gp. 281 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.12688/f1000research.18455.1 _zAvailable from publisher's website |
| 999 |
_c29828338 _d29828338 |
||