000 01002 a2200301 4500
005 20250511150837.0
264 0 _c19790925
008 197909s 0 0 eng d
022 _a0301-0171
024 7 _a10.1159/000131011
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aFerguson-Smith, M A
245 0 0 _aHeterozygosity at the alpha-haptoglobin locus associated with a deletion, 16q22 leads to 16qter.
_h[electronic resource]
260 _bCytogenetics and cell genetics
_c1978
300 _a513 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aChild
650 0 4 _aChromosome Deletion
650 0 4 _aChromosome Mapping
650 0 4 _aChromosomes, Human, 16-18
650 0 4 _aFemale
650 0 4 _aHaptoglobins
_xgenetics
650 0 4 _aHeterozygote
650 0 4 _aHumans
700 1 _aAitken, D A
773 0 _tCytogenetics and cell genetics
_gvol. 22
_gno. 1-6
_gp. 513
856 4 0 _uhttps://doi.org/10.1159/000131011
_zAvailable from publisher's website
999 _c772870
_d772870