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