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