000 00898 a2200289 4500
005 20250512170733.0
264 0 _c19680710
008 196807s 0 0 eng d
022 _a0018-0661
024 7 _a10.1111/j.1601-5223.1967.tb02118.x
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aHall, B
245 0 0 _aA case of monosomy G?
_h[electronic resource]
260 _bHereditas
_c1967
300 _a356-64 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aChromosome Aberrations
650 0 4 _aChromosome Disorders
650 0 4 _aChromosomes, Human, 21-22 and Y
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aMale
700 1 _aFredga, K
700 1 _aSvenningsen, N
773 0 _tHereditas
_gvol. 57
_gno. 3
_gp. 356-64
856 4 0 _uhttps://doi.org/10.1111/j.1601-5223.1967.tb02118.x
_zAvailable from publisher's website
999 _c5587979
_d5587979