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 |