000 01576 a2200469 4500
005 20250514063459.0
264 0 _c20040106
008 200401s 0 0 eng d
022 _a1552-4825
024 7 _a10.1002/ajmg.a.10164
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aVialard, François
245 0 0 _aMechanism of intrachromosomal triplications 15q11-q13: a new clinical report.
_h[electronic resource]
260 _bAmerican journal of medical genetics. Part A
_cApr 2003
300 _a229-34 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdult
650 0 4 _aCell Nucleus
_xultrastructure
650 0 4 _aChromosome Mapping
650 0 4 _aChromosomes, Human, Pair 15
650 0 4 _aCytogenetics
650 0 4 _aEpilepsy
_xgenetics
650 0 4 _aFamily Health
650 0 4 _aFemale
650 0 4 _aGene Duplication
650 0 4 _aGenetic Markers
650 0 4 _aHumans
650 0 4 _aIn Situ Hybridization, Fluorescence
650 0 4 _aIntellectual Disability
_xgenetics
650 0 4 _aMale
650 0 4 _aMeiosis
650 0 4 _aModels, Genetic
650 0 4 _aPedigree
700 1 _aMignon-Ravix, Cécile
700 1 _aParain, Dominique
700 1 _aDepetris, Danielle
700 1 _aPortnoï, Marie-France
700 1 _aMoirot, Hélène
700 1 _aMattei, Marie-Geneviève
773 0 _tAmerican journal of medical genetics. Part A
_gvol. 118A
_gno. 3
_gp. 229-34
856 4 0 _uhttps://doi.org/10.1002/ajmg.a.10164
_zAvailable from publisher's website
999 _c12466483
_d12466483