000 | 01926 a2200577 4500 | ||
---|---|---|---|
005 | 20250516094956.0 | ||
264 | 0 | _c20130110 | |
008 | 201301s 0 0 eng d | ||
022 | _a1097-6833 | ||
024 | 7 |
_a10.1016/j.jpeds.2012.04.045 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aSpengler, Sabrina | |
245 | 0 | 0 |
_aMolecular karyotyping as a relevant diagnostic tool in children with growth retardation with Silver-Russell features. _h[electronic resource] |
260 |
_bThe Journal of pediatrics _cNov 2012 |
||
300 |
_a933-42 p. _bdigital |
||
500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
650 | 0 | 4 | _aChild |
650 | 0 | 4 | _aChild, Preschool |
650 | 0 | 4 | _aChromosome Aberrations |
650 | 0 | 4 | _aChromosome Deletion |
650 | 0 | 4 |
_aChromosomes, Human, Pair 11 _xgenetics |
650 | 0 | 4 |
_aChromosomes, Human, Pair 7 _xgenetics |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 |
_aGenetic Markers _xgenetics |
650 | 0 | 4 |
_aGrowth Disorders _xdiagnosis |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aInfant |
650 | 0 | 4 |
_aKaryotyping _xmethods |
650 | 0 | 4 | _aMale |
650 | 0 | 4 | _aMutation |
650 | 0 | 4 | _aOligonucleotide Array Sequence Analysis |
650 | 0 | 4 | _aPhenotype |
650 | 0 | 4 | _aPolymorphism, Single Nucleotide |
650 | 0 | 4 |
_aSilver-Russell Syndrome _xdiagnosis |
700 | 1 | _aBegemann, Matthias | |
700 | 1 | _aOrtiz Brüchle, Nadina | |
700 | 1 | _aBaudis, Michael | |
700 | 1 | _aDenecke, Bernd | |
700 | 1 | _aKroisel, Peter Michael | |
700 | 1 | _aOehl-Jaschkowitz, Barbara | |
700 | 1 | _aSchulze, Bernd | |
700 | 1 | _aRaabe-Meyer, Gisela | |
700 | 1 | _aSpaich, Christiane | |
700 | 1 | _aBlümel, Peter | |
700 | 1 | _aJauch, Anna | |
700 | 1 | _aMoog, Ute | |
700 | 1 | _aZerres, Klaus | |
700 | 1 | _aEggermann, Thomas | |
773 | 0 |
_tThe Journal of pediatrics _gvol. 161 _gno. 5 _gp. 933-42 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.jpeds.2012.04.045 _zAvailable from publisher's website |
999 |
_c21850962 _d21850962 |