000 01218 a2200373 4500
005 20250513190131.0
264 0 _c19991227
008 199912s 0 0 eng d
022 _a1015-8146
040 _aNLM
_beng
_cNLM
100 1 _aGoossens, E
245 0 0 _aMosaic normal/15q11-q13 duplication associated with developmental delay but normal phenotype.
_h[electronic resource]
260 _bGenetic counseling (Geneva, Switzerland)
_c1999
300 _a133-6 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aCell Line
650 0 4 _aChild, Preschool
650 0 4 _aChromosome Aberrations
_xgenetics
650 0 4 _aChromosome Disorders
650 0 4 _aChromosomes, Human, Pair 15
_xgenetics
650 0 4 _aDNA Probes
650 0 4 _aDevelopmental Disabilities
_xgenetics
650 0 4 _aGene Duplication
650 0 4 _aHumans
650 0 4 _aIn Situ Hybridization, Fluorescence
_xmethods
650 0 4 _aKaryotyping
650 0 4 _aMale
650 0 4 _aMosaicism
_xgenetics
650 0 4 _aPhenotype
700 1 _aDecock, P
700 1 _aPotgieter, S
700 1 _aFryns, J P
773 0 _tGenetic counseling (Geneva, Switzerland)
_gvol. 10
_gno. 2
_gp. 133-6
999 _c10379975
_d10379975