000 01479 a2200421 4500
005 20250517024521.0
264 0 _c20160217
008 201602s 0 0 eng d
022 _a1552-4833
024 7 _a10.1002/ajmg.a.36846
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aKamien, Benjamin
245 0 0 _aCharacterization of a 520 kb deletion on chromosome 15q26.1 including ST8SIA2 in a patient with behavioral disturbance, autism spectrum disorder, and epilepsy: additional information.
_h[electronic resource]
260 _bAmerican journal of medical genetics. Part A
_cJun 2015
300 _a1424 p.
_bdigital
500 _aPublication Type: Case Reports; Letter
650 0 4 _aAdolescent
650 0 4 _aAutism Spectrum Disorder
_xgenetics
650 0 4 _aChromosome Deletion
650 0 4 _aChromosomes, Human, Pair 15
650 0 4 _aEpilepsy
_xgenetics
650 0 4 _aFathers
650 0 4 _aGene Deletion
650 0 4 _aGene Expression
650 0 4 _aHumans
650 0 4 _aInheritance Patterns
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aSialyltransferases
_xdeficiency
700 1 _aHarraway, James
700 1 _aLundie, Ben
700 1 _aSmallhorne, Lex
700 1 _aGibbs, Vicki
700 1 _aHeath, Anna
700 1 _aFullerton, Janice M
773 0 _tAmerican journal of medical genetics. Part A
_gvol. 167
_gno. 6
_gp. 1424
856 4 0 _uhttps://doi.org/10.1002/ajmg.a.36846
_zAvailable from publisher's website
999 _c24777841
_d24777841