000 00995 a2200337 4500
005 20250511133745.0
264 0 _c19790925
008 197909s 0 0 ita d
022 _a0026-4946
040 _aNLM
_beng
_cNLM
100 1 _aFerrante, E
245 0 0 _a[18p syndrome -- caused by 18/21 translocation].
_h[electronic resource]
260 _bMinerva pediatrica
_cApr 1979
300 _a657-64 p.
_bdigital
500 _aPublication Type: Case Reports; English Abstract; Journal Article
650 0 4 _aChild
650 0 4 _aChromosome Aberrations
650 0 4 _aChromosome Deletion
650 0 4 _aChromosomes, Human, 16-18
650 0 4 _aChromosomes, Human, 21-22 and Y
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aInfant, Newborn
650 0 4 _aSyndrome
650 0 4 _aTranslocation, Genetic
700 1 _aChessa, L
700 1 _aBruni, L
700 1 _aTozzi, M C
700 1 _aLo Cuoco, A
773 0 _tMinerva pediatrica
_gvol. 31
_gno. 8
_gp. 657-64
999 _c480545
_d480545