000 01436 a2200385 4500
005 20250515145423.0
264 0 _c20090428
008 200904s 0 0 eng d
022 _a1878-0849
024 7 _a10.1016/j.ejmg.2008.10.001
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aLespinasse, James
245 0 0 _aCharacterization of an interstitial deletion 6q13-q14.1 in a female with mild mental retardation, language delay and minor dysmorphisms.
_h[electronic resource]
260 _bEuropean journal of medical genetics
_c
300 _a49-52 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aChild
650 0 4 _aChromosome Deletion
650 0 4 _aChromosomes, Human, Pair 16
650 0 4 _aComparative Genomic Hybridization
650 0 4 _aFemale
650 0 4 _aGenotype
650 0 4 _aHumans
650 0 4 _aIntellectual Disability
_xgenetics
650 0 4 _aLanguage Development Disorders
_xgenetics
650 0 4 _aPhenotype
650 0 4 _aPsychomotor Disorders
_xgenetics
700 1 _aGimelli, Stefania
700 1 _aBéna, Frédérique
700 1 _aAntonarakis, Stylianos E
700 1 _aAnsermet, François
700 1 _aPaoloni-Giacobino, Ariane
773 0 _tEuropean journal of medical genetics
_gvol. 52
_gno. 1
_gp. 49-52
856 4 0 _uhttps://doi.org/10.1016/j.ejmg.2008.10.001
_zAvailable from publisher's website
999 _c18453278
_d18453278