000 01302 a2200385 4500
005 20250518013832.0
264 0 _c20191121
008 201911s 0 0 eng d
022 _a1545-5017
024 7 _a10.1002/pbc.27589
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aCsillag, Bernhard
245 0 0 _aSomatic mosaic monosomy 7 and UPD7q in a child with MIRAGE syndrome caused by a novel SAMD9 mutation.
_h[electronic resource]
260 _bPediatric blood & cancer
_c04 2019
300 _ae27589 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aChild, Preschool
650 0 4 _aChromosome Deletion
650 0 4 _aChromosomes, Human, Pair 7
650 0 4 _aHumans
650 0 4 _aIntracellular Signaling Peptides and Proteins
650 0 4 _aMale
650 0 4 _aMutation
650 0 4 _aMyelodysplastic Syndromes
_xgenetics
650 0 4 _aProteins
_xgenetics
700 1 _aIlencikova, Denisa
700 1 _aMeissl, Manfred
700 1 _aWebersinke, Gerald
700 1 _aLaccone, Franco
700 1 _aNarumi, Satoshi
700 1 _aHaas, Oskar
700 1 _aDuba, Hans-Christoph
773 0 _tPediatric blood & cancer
_gvol. 66
_gno. 4
_gp. e27589
856 4 0 _uhttps://doi.org/10.1002/pbc.27589
_zAvailable from publisher's website
999 _c29178556
_d29178556