000 01339 a2200385 4500
005 20250515002013.0
264 0 _c20051109
008 200511s 0 0 eng d
022 _a1769-7212
024 7 _a10.1016/j.ejmg.2005.04.012
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aPramparo, Tiziano
245 0 0 _aNarrowing the deleted region associated with the 15q21 syndrome.
_h[electronic resource]
260 _bEuropean journal of medical genetics
_c
300 _a346-52 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAbnormalities, Multiple
_xdiagnosis
650 0 4 _aChild, Preschool
650 0 4 _aChromosome Deletion
650 0 4 _aChromosome Disorders
_xdiagnosis
650 0 4 _aChromosomes, Human, Pair 15
_xgenetics
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aMale
650 0 4 _aNucleic Acid Hybridization
650 0 4 _aOligonucleotide Array Sequence Analysis
650 0 4 _aSyndrome
700 1 _aMattina, Teresa
700 1 _aGimelli, Stefania
700 1 _aLiehr, Thomas
700 1 _aZuffardi, Orsetta
773 0 _tEuropean journal of medical genetics
_gvol. 48
_gno. 3
_gp. 346-52
856 4 0 _uhttps://doi.org/10.1016/j.ejmg.2005.04.012
_zAvailable from publisher's website
999 _c15811079
_d15811079