000 01181 a2200349 4500
005 20250518025946.0
264 0 _c20190325
008 201903s 0 0 eng d
022 _a1536-5964
024 7 _a10.1097/MD.0000000000014782
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aBravo-Gil, Nereida
245 0 0 _aExpanding the clinical and mutational spectrum of germline ABL1 mutations-associated syndrome: A case report.
_h[electronic resource]
260 _bMedicine
_cMar 2019
300 _ae14782 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAbnormalities, Multiple
_xdiagnosis
650 0 4 _aDiagnosis, Differential
650 0 4 _aGerm-Line Mutation
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aMale
650 0 4 _aPhenotype
650 0 4 _aProto-Oncogene Proteins c-abl
_xgenetics
650 0 4 _aSyndrome
700 1 _aMarcos, Irene
700 1 _aGonzález-Meneses, Antonio
700 1 _aAntiñolo, Guillermo
700 1 _aBorrego, Salud
773 0 _tMedicine
_gvol. 98
_gno. 10
_gp. e14782
856 4 0 _uhttps://doi.org/10.1097/MD.0000000000014782
_zAvailable from publisher's website
999 _c29462065
_d29462065