000 01454 a2200445 4500
005 20250513060217.0
264 0 _c19940922
008 199409s 0 0 eng d
022 _a0022-2593
024 7 _a10.1136/jmg.31.5.413
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aD'Alessandro, E
245 0 0 _aPartial monosomy of 7q32 in a case of de novo rcp(7;15)(q32;q15).
_h[electronic resource]
260 _bJournal of medical genetics
_cMay 1994
300 _a413-5 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAbnormalities, Multiple
_xgenetics
650 0 4 _aChild, Preschool
650 0 4 _aChromosome Aberrations
_xgenetics
650 0 4 _aChromosome Deletion
650 0 4 _aChromosome Disorders
650 0 4 _aChromosomes, Human, Pair 15
650 0 4 _aChromosomes, Human, Pair 7
650 0 4 _aDwarfism
_xgenetics
650 0 4 _aFace
_xabnormalities
650 0 4 _aFemale
650 0 4 _aFingers
_xabnormalities
650 0 4 _aHumans
650 0 4 _aIntellectual Disability
_xgenetics
650 0 4 _aKaryotyping
650 0 4 _aMicrocephaly
_xgenetics
650 0 4 _aTranslocation, Genetic
700 1 _aLigas, C
700 1 _aLo Re, M L
700 1 _aMarcanio, M P
700 1 _aGentile, T
700 1 _aDel Porto, G
773 0 _tJournal of medical genetics
_gvol. 31
_gno. 5
_gp. 413-5
856 4 0 _uhttps://doi.org/10.1136/jmg.31.5.413
_zAvailable from publisher's website
999 _c8064149
_d8064149