000 01478 a2200445 4500
005 20250518025358.0
264 0 _c20200930
008 202009s 0 0 eng d
022 _a1878-0849
024 7 _a10.1016/j.ejmg.2019.02.008
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aRepnikova, Elena A
245 0 0 _aCNTN6 copy number variations: Uncertain clinical significance in individuals with neurodevelopmental disorders.
_h[electronic resource]
260 _bEuropean journal of medical genetics
_cJan 2020
300 _a103636 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAdolescent
650 0 4 _aChild
650 0 4 _aContactins
_xgenetics
650 0 4 _aFemale
650 0 4 _aGene Dosage
_xgenetics
650 0 4 _aGenetic Association Studies
650 0 4 _aGenetic Predisposition to Disease
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMicroarray Analysis
650 0 4 _aNeurodevelopmental Disorders
_xdiagnosis
650 0 4 _aPhenotype
700 1 _aLyalin, Dmitry A
700 1 _aMcDonald, Kimberly
700 1 _aAstbury, Caroline
700 1 _aHansen-Kiss, Emily
700 1 _aCooley, Linda D
700 1 _aPfau, Ruthann
700 1 _aHerman, Gail E
700 1 _aPyatt, Robert E
700 1 _aHickey, Scott E
773 0 _tEuropean journal of medical genetics
_gvol. 63
_gno. 1
_gp. 103636
856 4 0 _uhttps://doi.org/10.1016/j.ejmg.2019.02.008
_zAvailable from publisher's website
999 _c29443141
_d29443141