000 01374 a2200397 4500
005 20250517191645.0
264 0 _c20180903
008 201809s 0 0 eng d
022 _a1473-5717
024 7 _a10.1097/MCD.0000000000000209
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aSchirwani, Schaida
245 0 0 _aClinical and molecular characterization of the first familial report of 1p32 microdeletion.
_h[electronic resource]
260 _bClinical dysmorphology
_cApr 2018
300 _a36-41 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAbnormalities, Multiple
_xgenetics
650 0 4 _aAdult
650 0 4 _aChromosome Deletion
650 0 4 _aChromosomes, Human, Pair 1
_xgenetics
650 0 4 _aComparative Genomic Hybridization
650 0 4 _aDNA-Binding Proteins
_xgenetics
650 0 4 _aDevelopmental Disabilities
_xgenetics
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aLDL-Receptor Related Proteins
_xgenetics
650 0 4 _aMale
650 0 4 _aMicrocephaly
_xgenetics
650 0 4 _aPedigree
650 0 4 _aPhenotype
650 0 4 _aTranscription Factors
_xgenetics
700 1 _aSmith, Kath
700 1 _aBalasubramanian, Meena
773 0 _tClinical dysmorphology
_gvol. 27
_gno. 2
_gp. 36-41
856 4 0 _uhttps://doi.org/10.1097/MCD.0000000000000209
_zAvailable from publisher's website
999 _c27888983
_d27888983