000 | 01219 a2200373 4500 | ||
---|---|---|---|
005 | 20250513045043.0 | ||
264 | 0 | _c19950302 | |
008 | 199503s 0 0 eng d | ||
022 | _a0009-9163 | ||
024 | 7 |
_a10.1111/j.1399-0004.1994.tb04162.x _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aHertz, J M | |
245 | 0 | 0 |
_aCharcot-Marie-Tooth disease type 1A: the parental origin of a de novo 17p11.2-p12 duplication. _h[electronic resource] |
260 |
_bClinical genetics _cOct 1994 |
||
300 |
_a291-4 p. _bdigital |
||
500 | _aPublication Type: Journal Article | ||
650 | 0 | 4 | _aAdult |
650 | 0 | 4 |
_aCharcot-Marie-Tooth Disease _xgenetics |
650 | 0 | 4 | _aChromosome Aberrations |
650 | 0 | 4 | _aChromosomes, Human, Pair 17 |
650 | 0 | 4 | _aDNA Mutational Analysis |
650 | 0 | 4 | _aFathers |
650 | 0 | 4 | _aGenomic Imprinting |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aMale |
650 | 0 | 4 | _aPedigree |
650 | 0 | 4 | _aRepetitive Sequences, Nucleic Acid |
700 | 1 | _aBørglum, A D | |
700 | 1 | _aBrandt, C A | |
700 | 1 | _aFlint, T | |
700 | 1 | _aBisgaard, C | |
773 | 0 |
_tClinical genetics _gvol. 46 _gno. 4 _gp. 291-4 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1111/j.1399-0004.1994.tb04162.x _zAvailable from publisher's website |
999 |
_c7834230 _d7834230 |