000 01394 a2200397 4500
005 20250512085154.0
264 0 _c19851213
008 198512s 0 0 eng d
022 _a0148-7299
024 7 _a10.1002/ajmg.1320220316
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aDaniel, A
245 0 0 _aNOR activity and centromere suppression related in a de novo fusion tdic(9;13)(p22;p13) chromosome in a child with del(9p) syndrome.
_h[electronic resource]
260 _bAmerican journal of medical genetics
_cNov 1985
300 _a577-84 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aCentromere
_xphysiology
650 0 4 _aChromosome Aberrations
_xgenetics
650 0 4 _aChromosome Banding
650 0 4 _aChromosome Deletion
650 0 4 _aChromosome Disorders
650 0 4 _aChromosomes
_xphysiology
650 0 4 _aChromosomes, Human, 6-12 and X
650 0 4 _aDermatoglyphics
650 0 4 _aFemale
650 0 4 _aGene Expression Regulation
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aNucleolus Organizer Region
_xphysiology
700 1 _aEkblom, L
700 1 _aPhillips, S
700 1 _aFitzGerald, J M
700 1 _aOpitz, J M
773 0 _tAmerican journal of medical genetics
_gvol. 22
_gno. 3
_gp. 577-84
856 4 0 _uhttps://doi.org/10.1002/ajmg.1320220316
_zAvailable from publisher's website
999 _c4067173
_d4067173