000 01368 a2200385 4500
005 20250513153537.0
264 0 _c19990105
008 199901s 0 0 eng d
022 _a0022-2593
024 7 _a10.1136/jmg.35.10.829
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMatsumoto, N
245 0 0 _aIsolation of BAC clones spanning the Xq22.3 translocation breakpoint in a lissencephaly patient with a de novo X;2 translocation.
_h[electronic resource]
260 _bJournal of medical genetics
_cOct 1998
300 _a829-32 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aBrain
_xabnormalities
650 0 4 _aChromosomes, Bacterial
_xgenetics
650 0 4 _aChromosomes, Human, Pair 2
650 0 4 _aContig Mapping
650 0 4 _aElectrophoresis, Gel, Pulsed-Field
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aIn Situ Hybridization, Fluorescence
650 0 4 _aSequence Analysis, DNA
650 0 4 _aSequence Tagged Sites
650 0 4 _aTranslocation, Genetic
650 0 4 _aX Chromosome
700 1 _aPilz, D T
700 1 _aFantes, J A
700 1 _aKittikamron, K
700 1 _aLedbetter, D H
773 0 _tJournal of medical genetics
_gvol. 35
_gno. 10
_gp. 829-32
856 4 0 _uhttps://doi.org/10.1136/jmg.35.10.829
_zAvailable from publisher's website
999 _c9748262
_d9748262