000 01518 a2200433 4500
005 20250515023754.0
264 0 _c20060727
008 200607s 0 0 eng d
022 _a1552-4825
024 7 _a10.1002/ajmg.a.31229
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aLennon, P A
245 0 0 _aWAGR(O?) syndrome and congenital ptosis caused by an unbalanced t(11;15)(p13;p11.2)dn demonstrating a 7 megabase deletion by FISH.
_h[electronic resource]
260 _bAmerican journal of medical genetics. Part A
_cJun 2006
300 _a1214-8 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAbnormalities, Multiple
_xgenetics
650 0 4 _aBlepharoptosis
_xpathology
650 0 4 _aChromosome Banding
650 0 4 _aChromosome Deletion
650 0 4 _aChromosomes, Human, Pair 11
_xgenetics
650 0 4 _aChromosomes, Human, Pair 15
_xgenetics
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aIn Situ Hybridization, Fluorescence
650 0 4 _aInfant
650 0 4 _aKaryotyping
650 0 4 _aObesity
_xpathology
650 0 4 _aTranslocation, Genetic
650 0 4 _aWAGR Syndrome
_xpathology
700 1 _aScott, D A
700 1 _aLonsdorf, D
700 1 _aWargowski, D S
700 1 _aKirkpatrick, S
700 1 _aPatel, A
700 1 _aCheung, S W
773 0 _tAmerican journal of medical genetics. Part A
_gvol. 140
_gno. 11
_gp. 1214-8
856 4 0 _uhttps://doi.org/10.1002/ajmg.a.31229
_zAvailable from publisher's website
999 _c16248487
_d16248487