000 01475 a2200433 4500
005 20250515060226.0
264 0 _c20070508
008 200705s 0 0 eng d
022 _a1552-4825
024 7 _a10.1002/ajmg.a.31614
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aBarber, John C K
245 0 0 _aTransmitted duplication of 12q21.32-12q22 includes 48 genes and has no apparent phenotypic consequences.
_h[electronic resource]
260 _bAmerican journal of medical genetics. Part A
_cMar 2007
300 _a615-8 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAdult
650 0 4 _aChild, Preschool
650 0 4 _aChromosome Aberrations
650 0 4 _aChromosome Banding
650 0 4 _aChromosome Disorders
_xdiagnosis
650 0 4 _aChromosomes, Human, Pair 12
_xgenetics
650 0 4 _aFamily Health
650 0 4 _aFemale
650 0 4 _aGene Duplication
650 0 4 _aGenome, Human
650 0 4 _aHumans
650 0 4 _aIn Situ Hybridization, Fluorescence
650 0 4 _aKaryotyping
650 0 4 _aNucleic Acid Hybridization
_xmethods
650 0 4 _aPhenotype
700 1 _aMaloney, Viv K
700 1 _aKirchhoff, Maria
700 1 _aThomas, N Simon
700 1 _aBoyle, Tracy A
700 1 _aCastle, Bruce
773 0 _tAmerican journal of medical genetics. Part A
_gvol. 143A
_gno. 6
_gp. 615-8
856 4 0 _uhttps://doi.org/10.1002/ajmg.a.31614
_zAvailable from publisher's website
999 _c16876930
_d16876930