000 01075 a2200325 4500
005 20250512060301.0
264 0 _c19870219
008 198702s 0 0 eng d
022 _a0032-5473
024 7 _a10.1136/pgmj.62.724.131
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aPembrey, M
245 0 0 _aRecently recognized chromosomal defects of clinical importance.
_h[electronic resource]
260 _bPostgraduate medical journal
_cFeb 1986
300 _a131-42 p.
_bdigital
500 _aPublication Type: Journal Article; Review
650 0 4 _aChromosome Aberrations
_xdiagnosis
650 0 4 _aChromosome Deletion
650 0 4 _aChromosome Disorders
650 0 4 _aFemale
650 0 4 _aFragile X Syndrome
_xgenetics
650 0 4 _aGenetic Linkage
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aTranslocation, Genetic
650 0 4 _aX Chromosome
700 1 _aBaraitser, M
773 0 _tPostgraduate medical journal
_gvol. 62
_gno. 724
_gp. 131-42
856 4 0 _uhttps://doi.org/10.1136/pgmj.62.724.131
_zAvailable from publisher's website
999 _c3546650
_d3546650