000 01502 a2200433 4500
005 20250516085542.0
264 0 _c20121026
008 201210s 0 0 eng d
022 _a1552-4833
024 7 _a10.1002/ajmg.a.35311
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aKvarnung, Malin
245 0 0 _aInherited mosaicism for the supernumerary marker chromosome in cat eye syndrome: inter- and intra-individual variation and correlation to the phenotype.
_h[electronic resource]
260 _bAmerican journal of medical genetics. Part A
_cMay 2012
300 _a1111-7 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAneuploidy
650 0 4 _aChild
650 0 4 _aChromosome Disorders
_xgenetics
650 0 4 _aChromosomes, Human, Pair 22
_xgenetics
650 0 4 _aEye Abnormalities
650 0 4 _aFamily
650 0 4 _aGenetic Markers
650 0 4 _aHumans
650 0 4 _aIn Situ Hybridization, Fluorescence
650 0 4 _aMale
650 0 4 _aMosaicism
650 0 4 _aPhenotype
650 0 4 _aSpermatozoa
700 1 _aLindstrand, Anna
700 1 _aMalmgren, Helena
700 1 _aThåström, Anders
700 1 _aJacobson, Lena
700 1 _aDahl, Niklas
700 1 _aLundin, Johanna
700 1 _aBlennow, Elisabeth
773 0 _tAmerican journal of medical genetics. Part A
_gvol. 158A
_gno. 5
_gp. 1111-7
856 4 0 _uhttps://doi.org/10.1002/ajmg.a.35311
_zAvailable from publisher's website
999 _c21697328
_d21697328