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 |