000 01635 a2200517 4500
005 20250514160358.0
264 0 _c20040319
008 200403s 0 0 eng d
022 _a1526-632X
024 7 _a10.1212/wnl.61.7.909
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aWohlgemuth, M
245 0 0 _aPossible phenotypic dosage effect in patients compound heterozygous for FSHD-sized 4q35 alleles.
_h[electronic resource]
260 _bNeurology
_cOct 2003
300 _a909-13 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAged
650 0 4 _aAlleles
650 0 4 _aChromosomes, Human, Pair 4
_xgenetics
650 0 4 _aCytogenetic Analysis
650 0 4 _aElectrophoresis, Gel, Pulsed-Field
650 0 4 _aFemale
650 0 4 _aGene Dosage
650 0 4 _aGenes, Dominant
650 0 4 _aHeterozygote
650 0 4 _aHumans
650 0 4 _aIn Situ Hybridization, Fluorescence
650 0 4 _aMale
650 0 4 _aMuscular Dystrophy, Facioscapulohumeral
_xgenetics
650 0 4 _aPedigree
650 0 4 _aPenetrance
650 0 4 _aPhenotype
650 0 4 _aRepetitive Sequences, Nucleic Acid
650 0 4 _aRestriction Mapping
700 1 _aLemmers, R J
700 1 _avan der Kooi, E L
700 1 _avan der Wielen, M J
700 1 _avan Overveld, P G
700 1 _aDauwerse, H
700 1 _aBakker, E
700 1 _aFrants, R R
700 1 _aPadberg, G W
700 1 _avan der Maarel, S M
773 0 _tNeurology
_gvol. 61
_gno. 7
_gp. 909-13
856 4 0 _uhttps://doi.org/10.1212/wnl.61.7.909
_zAvailable from publisher's website
999 _c14300813
_d14300813