000 01382 a2200433 4500
005 20250513070946.0
264 0 _c19940209
008 199402s 0 0 eng d
022 _a0009-9163
024 7 _a10.1111/j.1399-0004.1993.tb03869.x
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aSpeleman, F
245 0 0 _aMolecular cytogenetic analysis of a familial pericentric inversion of chromosome 12.
_h[electronic resource]
260 _bClinical genetics
_cSep 1993
300 _a156-63 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAdult
650 0 4 _aChromosome Banding
650 0 4 _aChromosome Inversion
650 0 4 _aChromosomes, Human, Pair 12
650 0 4 _aDNA Probes
650 0 4 _aFailure to Thrive
_xgenetics
650 0 4 _aFemale
650 0 4 _aFollow-Up Studies
650 0 4 _aHumans
650 0 4 _aIn Situ Hybridization, Fluorescence
_xmethods
650 0 4 _aInfant, Newborn
650 0 4 _aIntellectual Disability
_xgenetics
650 0 4 _aMale
650 0 4 _aPedigree
650 0 4 _aSyndrome
700 1 _aVan Roy, N
700 1 _aDe Vos, E
700 1 _aHilliker, C
700 1 _aSuijkerbuijk, R F
700 1 _aLeroy, J G
773 0 _tClinical genetics
_gvol. 44
_gno. 3
_gp. 156-63
856 4 0 _uhttps://doi.org/10.1111/j.1399-0004.1993.tb03869.x
_zAvailable from publisher's website
999 _c8274858
_d8274858