000 01118 a2200313 4500
005 20250515090825.0
264 0 _c20080117
008 200801s 0 0 eng d
022 _a1552-4876
024 7 _a10.1002/ajmg.c.30151
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aRauch, Anita
245 0 0 _aChromosome 5q subtelomeric deletion syndrome.
_h[electronic resource]
260 _bAmerican journal of medical genetics. Part C, Seminars in medical genetics
_cNov 2007
300 _a372-6 p.
_bdigital
500 _aPublication Type: Journal Article; Review
650 0 4 _aChromosome Mapping
650 0 4 _aChromosomes, Human, Pair 5
_xgenetics
650 0 4 _aGene Deletion
650 0 4 _aHumans
650 0 4 _aIn Situ Hybridization, Fluorescence
650 0 4 _aKaryotyping
650 0 4 _aPhenotype
650 0 4 _aSyndrome
650 0 4 _aTelomere
700 1 _aDörr, Helmuth-Günther
773 0 _tAmerican journal of medical genetics. Part C, Seminars in medical genetics
_gvol. 145C
_gno. 4
_gp. 372-6
856 4 0 _uhttps://doi.org/10.1002/ajmg.c.30151
_zAvailable from publisher's website
999 _c17431753
_d17431753