000 01376 a2200409 4500
005 20250511170208.0
264 0 _c19750820
008 197508s 0 0 eng d
022 _a0009-9163
024 7 _a10.1111/j.1399-0004.1975.tb00309.x
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aOrye, E
245 0 0 _aA new case of the trisomy 9P syndrome. Report of a patient with unusual chromosome findings (46,XX/47,XX, + i (9p) and a peculiar congenital heart defect.
_h[electronic resource]
260 _bClinical genetics
_cFeb 1975
300 _a134-43 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAbnormalities, Multiple
_xgenetics
650 0 4 _aAneuploidy
650 0 4 _aChromosomes, Human, 6-12 and X
650 0 4 _aCleft Palate
_xgenetics
650 0 4 _aFace
_xabnormalities
650 0 4 _aFemale
650 0 4 _aHeart Defects, Congenital
_xgenetics
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aInfant, Newborn
650 0 4 _aKaryotyping
650 0 4 _aLip
_xabnormalities
650 0 4 _aMosaicism
650 0 4 _aPedigree
650 0 4 _aTrisomy
700 1 _aVerhaaren, H
700 1 _aVan Egmond, H
700 1 _aDevloo-Blancquaert, A
773 0 _tClinical genetics
_gvol. 7
_gno. 2
_gp. 134-43
856 4 0 _uhttps://doi.org/10.1111/j.1399-0004.1975.tb00309.x
_zAvailable from publisher's website
999 _c1138850
_d1138850