000 01490 a2200469 4500
005 20250512144949.0
264 0 _c19720627
008 197206s 0 0 eng d
022 _a0011-4537
024 7 _a10.1159/000130161
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aWeber, F M
245 0 0 _aDouble monosomy mosaicism (45,X-45, XX,21-) in a retarded child with multiple congenital malformations.
_h[electronic resource]
260 _bCytogenetics
_c1971
300 _a404-12 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAbnormalities, Multiple
_xgenetics
650 0 4 _aAneuploidy
650 0 4 _aAutoradiography
650 0 4 _aBlood Protein Electrophoresis
650 0 4 _aBone Marrow Cells
650 0 4 _aChild, Preschool
650 0 4 _aChromosomes, Human, 21-22 and Y
650 0 4 _aFemale
650 0 4 _aFibroblasts
_xcytology
650 0 4 _aHair
_xcytology
650 0 4 _aHumans
650 0 4 _aIntellectual Disability
_xgenetics
650 0 4 _aKaryotyping
650 0 4 _aLymphocytes
_xcytology
650 0 4 _aMicroscopy, Fluorescence
650 0 4 _aMosaicism
650 0 4 _aMouth Mucosa
_xcytology
650 0 4 _aSex Chromatin
650 0 4 _aSex Chromosome Aberrations
650 0 4 _aThymidine
_xmetabolism
650 0 4 _aTritium
700 1 _aSparkes, R S
700 1 _aMuller, H
773 0 _tCytogenetics
_gvol. 10
_gno. 6
_gp. 404-12
856 4 0 _uhttps://doi.org/10.1159/000130161
_zAvailable from publisher's website
999 _c5148643
_d5148643