| 000 | 01512 a2200445 4500 | ||
|---|---|---|---|
| 005 | 20250517153420.0 | ||
| 264 | 0 | _c20180326 | |
| 008 | 201803s 0 0 eng d | ||
| 022 | _a1791-3004 | ||
| 024 | 7 |
_a10.3892/mmr.2017.6569 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aSi, Yan-Mei | |
| 245 | 0 | 0 |
_aHypospadias in a male infant with an unusual mosaic 45,X/46,X,psu idic(Y)(p11.32)/46,XY and haploinsufficiency of SHOX: A case report. _h[electronic resource] |
| 260 |
_bMolecular medicine reports _cJul 2017 |
||
| 300 |
_a201-207 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 | _aBiomarkers |
| 650 | 0 | 4 | _aChromosome Aberrations |
| 650 | 0 | 4 | _aChromosomes, Human, X |
| 650 | 0 | 4 | _aChromosomes, Human, Y |
| 650 | 0 | 4 | _aComparative Genomic Hybridization |
| 650 | 0 | 4 | _aGenetic Association Studies |
| 650 | 0 | 4 | _aHaploinsufficiency |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aHypospadias _xdiagnosis |
| 650 | 0 | 4 | _aIn Situ Hybridization, Fluorescence |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 | _aKaryotyping |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMosaicism |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aPolymorphism, Single Nucleotide |
| 650 | 0 | 4 |
_aShort Stature Homeobox Protein _xgenetics |
| 700 | 1 | _aDong, Yuan | |
| 700 | 1 | _aWang, Wei | |
| 700 | 1 | _aQi, Ke-Yan | |
| 700 | 1 | _aWang, Xin | |
| 773 | 0 |
_tMolecular medicine reports _gvol. 16 _gno. 1 _gp. 201-207 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.3892/mmr.2017.6569 _zAvailable from publisher's website |
| 999 |
_c27167629 _d27167629 |
||