000 | 01195 a2200337 4500 | ||
---|---|---|---|
005 | 20250517210259.0 | ||
264 | 0 | _c20190321 | |
008 | 201903s 0 0 eng d | ||
022 | _a1878-0849 | ||
024 | 7 |
_a10.1016/j.ejmg.2018.03.009 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aBayat, Allan | |
245 | 0 | 0 |
_aNeonatal hyperinsulinemic hypoglycemia in a patient with 9p deletion syndrome. _h[electronic resource] |
260 |
_bEuropean journal of medical genetics _cAug 2018 |
||
300 |
_a473-477 p. _bdigital |
||
500 | _aPublication Type: Case Reports; Journal Article | ||
650 | 0 | 4 |
_aAbnormalities, Multiple _xgenetics |
650 | 0 | 4 | _aChromosome Deletion |
650 | 0 | 4 |
_aChromosome Disorders _xgenetics |
650 | 0 | 4 |
_aChromosomes, Human, Pair 9 _xgenetics |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 |
_aHyperinsulinism _xgenetics |
650 | 0 | 4 |
_aHypoglycemia _xgenetics |
650 | 0 | 4 | _aInfant |
650 | 0 | 4 | _aMale |
700 | 1 | _aKirchhoff, Maria | |
700 | 1 | _aMadsen, Camilla Gøbel | |
700 | 1 | _aKreiborg, Sven | |
773 | 0 |
_tEuropean journal of medical genetics _gvol. 61 _gno. 8 _gp. 473-477 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.ejmg.2018.03.009 _zAvailable from publisher's website |
999 |
_c28235018 _d28235018 |