000 02053 a2200709 4500
005 20250515103505.0
264 0 _c20080811
008 200808s 0 0 eng d
022 _a1468-6244
024 7 _a10.1136/jmg.2007.055830
_2doi
040 _aNLM
_beng
_cNLM
100 1 _avan Bon, B W M
245 0 0 _aClinical and molecular characteristics of 1qter microdeletion syndrome: delineating a critical region for corpus callosum agenesis/hypogenesis.
_h[electronic resource]
260 _bJournal of medical genetics
_cJun 2008
300 _a346-54 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aAgenesis of Corpus Callosum
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aChromosome Deletion
650 0 4 _aChromosomes, Human, Pair 1
_xgenetics
650 0 4 _aFamily
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aMale
650 0 4 _aSyndrome
700 1 _aKoolen, D A
700 1 _aBorgatti, R
700 1 _aMagee, A
700 1 _aGarcia-Minaur, S
700 1 _aRooms, L
700 1 _aReardon, W
700 1 _aZollino, M
700 1 _aBonaglia, M C
700 1 _aDe Gregori, M
700 1 _aNovara, F
700 1 _aGrasso, R
700 1 _aCiccone, R
700 1 _avan Duyvenvoorde, H A
700 1 _aAalbers, A M
700 1 _aGuerrini, R
700 1 _aFazzi, E
700 1 _aNillesen, W M
700 1 _aMcCullough, S
700 1 _aKant, S G
700 1 _aMarcelis, C L
700 1 _aPfundt, R
700 1 _ade Leeuw, N
700 1 _aSmeets, D
700 1 _aSistermans, E A
700 1 _aWit, J M
700 1 _aHamel, B C
700 1 _aBrunner, H G
700 1 _aKooy, F
700 1 _aZuffardi, O
700 1 _ade Vries, B B A
773 0 _tJournal of medical genetics
_gvol. 45
_gno. 6
_gp. 346-54
856 4 0 _uhttps://doi.org/10.1136/jmg.2007.055830
_zAvailable from publisher's website
999 _c17688671
_d17688671